Lead recalls (page 2)
349 recalls.
- INFINION CX LEAD KIT recall (Boston Scientific Neuromodulation Corporation)
Medical deviceClass IReported August 12, 2026 · Spinal cord stimulation system lead body may be exposed to stress at the anchor site. This may result in high impedance measurements or lead fractures, which... - Flow Anesthesia Machine Flow-i C20 6677200 Flow-i C30 6677300 Flow-i C40 6677400 ... recall (Maquet Critical Care AB)
Medical deviceClass IIReported August 12, 2026 · Events observed where anesthetic agent was not delivered when the vaporizer was activated. Failure to deliver the anesthetic agent may result in the patient... - Anti-Torque recall (Innovasis, Inc)
Medical deviceClass IIReported August 12, 2026 · Pedicle screw system intended to provide immobilization/stabilization of spinal segments as adjunct to thoracic/lumbar/sacral spine fusion may have anti-torque... - OsteoBallast recall (IsoTis OrthoBiologics, Inc.)
Medical deviceClass IIReported August 5, 2026 · Demineralized bone matrix (DBM) in resorbable mesh indicated for use with autograft as a bone graft extender in the posterolateral spine and pelvis, were... - L-Cath Midline S/L Catheter 20ga recall (Argon Medical Devices, Inc)
Medical deviceClass IIReported August 5, 2026 · Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may... - L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga recall (Argon Medical Devices, Inc)
Medical deviceClass IIReported August 5, 2026 · Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may... - Brooklyn Roasting Company Pasteurized Cold Brew Concentrate recall (Brooklyn Roasting Works LLC)
FoodClass IIReported July 29, 2026 · Ambient storage of the product may lead to Clostridium botulinum toxin formation. - MiniMed Go App recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported July 29, 2026 · For MiniMed Go app version 1.0.0 and 1.1.0, when the Set day and night is turned OFF and missed dose or Correct high glucose alerts are enabled, the... - ST AIA-Pack Testosterone recall (Tosoh Bioscience Inc)
Medical deviceClass IIReported July 22, 2026 · The Test cup lot F level 1 low-quality control results values for the device were lower than expected on the Automated Immunoassay Analyzer (AIA) which could... - Rapid Refill Continuous Injection System recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 22, 2026 · Devices contain recalled Medline Namic Angiographic Control Syringe with Rotating Adaptor. There is a risk of syringe loosening or disconnecting from the... - Warren James Recalls the Copper Cup Found in Flashgitz Relic Lunch Boxes Due to Risk of Serious Injury or Death from Lead Poisoning
Consumer productReported July 17, 2026 · The cup in the lunch boxes contains high lead concentration levels for drinking vessels, posing a lead poisoning hazard. Lead is toxic if ingested by adults or... - MiniMed 780G Insulin Pump recall (Medtronic MiniMed, Inc.)
Medical deviceClass IIReported July 15, 2026 · A software anomaly can occur when the pump is paired with the Instinct sensor. Under certain circumstances, the pump unexpectedly stops delivering insulin and... - Intracept Access Instruments recall (Boston Scientific Neuromodulation Corporation)
Medical deviceClass IIReported July 15, 2026 · Intraosseous nerve ablation system instruments may have sterile barrier breach of the outer tray seal, which may introduce a risk of sterility breach, and if... - Brand Name: Medela Product Name: ENFit ExSet Strl 60 2.0ml PV 1ct EN Model/Catalog... recall (Medela Inc)
Medical deviceClass IIReported July 8, 2026 · May contain incorrect connectors and will not attach or misconnect to ENFit connections and is thus incompatible. Issue could lead to slight delay in delivery... - Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401206RH recall (Medline Industries, LP)
Medical deviceClass IReported July 8, 2026 · Expansion of RES 98277. Specific lots of reprocessed catheters may contain small particles of residual material. If devices with residual particulates on... - Medline Convenience kits containing recalled Swan-Ganz Catheters CABG A CDS ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters OPEN HEART ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters CV ANESTHESIA -... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters KIT GERMANTOWN... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters CENTRAL AND... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters CARDIAC MAJOR ... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Medline Convenience kits containing recalled Swan-Ganz Catheters RIGHT HEART CATH... recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal... - Omnipod recall (Insulet Corporation)
Medical deviceClass IReported July 8, 2026 · External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or... - Omnipod DASH Pod. Includes the below Model/REF Numbers: 1. POD-BLE-I1-525 recall (Insulet Corporation)
Medical deviceClass IReported July 8, 2026 · External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or... - Omnipod 5 Pods. Includes the below Model/REF Numbers: 1. POD-OMNI-I1-6720. 2.... recall (Insulet Corporation)
Medical deviceClass IReported July 8, 2026 · External soft cannula damage during manufacturing that results in insulin leaking around the Pod instead of being delivered to the user regardless of basal or... - Hillrom VOLARA System P.CIRCUIT 5KIT AC recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Hillrom VOLARA System P.CIRCUIT KIT AC recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Hillrom VOLARA P.CIRCUIT 5KIT recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Hillrom VOLARA System P.CIRCUIT KIT recall (Baxter Healthcare Corporation)
Medical deviceClass IReported July 8, 2026 · There have been reports of air and medication leakage from the nebulizer cup during therapy of Volara system patient circuits. The leakage can lead to an... - Philips Telemetry Monitor 5500 1.4 GHz. Model Number: 867232. Includes the following... recall (Philips North America Llc)
Medical deviceClass IIReported July 1, 2026 · Potential for device reset to default "NEW_DEVICE" state, which may lead to a to loss of device configuration and the equipment label, resulting in a failure... - GE Healthcare AW Server 3.2 ext.6.5 recall (GE Medical Systems SCS)
Medical deviceClass IIReported July 1, 2026 · GE HealthCare has become aware of a context synchronization issue in AW Server 3.2 ext. 6.5. When a user selects a patient or exam in the AW Server Web Client... - Brand Name: Inspire Medical Systems recall (Inspire Medical Systems Inc.)
Medical deviceClass IIReported June 24, 2026 · Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation of a... - Brand Name: Inspire Medical Systems recall (Inspire Medical Systems Inc.)
Medical deviceClass IIReported June 24, 2026 · Products are labeled with incorrect Use By Date, extending beyond the validated three-year shelf life from date of manufacturer. Material degradation of a... - Ritmed Neurological Sponges recall (AMD Medicom Inc.)
Medical deviceClass IIReported June 24, 2026 · Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during incision, may not... - Ritmed Neurological Sponges recall (AMD Medicom Inc.)
Medical deviceClass IIReported June 24, 2026 · Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to protect the brain during incision, may not... - TRIGEN PROXIMAL STRAIGHT HUMERAL NAIL 8/7 X 16 recall (Smith & Nephew, Inc.)
Medical deviceClass IIReported June 24, 2026 · Humeral nail due to a manufacturing error is missing distal holes and if implanted may lead to revision surgery but, if the missing holes are identified before... - Description/REF: RA CATH KIT: 20 GA X 1-1/2IN/NA-04220-1A recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: CVC KIT: 16 GA X 8IN/AK-04210 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PICC ACCESS TRAY/ASK-04001-CG1 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: MIDLINE CATHETER KIT: 3 FR X 20 CM/CDC-02031-MK1A recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PSI KIT: 7 FR X 4 IN/ASK-09701-UP recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ACCESS TRAY/ASK-04001-MC3 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: RA CATH KIT: 20 GA X 1-3/4IN/AK-04020-SPC recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: SAC KIT: 18 GA X 12CM W BIO/SAC-01218-B recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: SPINAL ANESTHESIA KIT/ASA-24090-SB recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 20 CM/AK-15122-F recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PI MIDLINE 2L: 5FR X 20CM/CDC-32052-MPKC recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PARACENTESIS KIT/ASK-00376-JHH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ACCESS TRAY/GU-04020 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ACCESS TRAY/ASK-04001-JHH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PACING/PSI KIT: 5 FR 2L/ASK-07155-MGU recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: DRAINAGE KIT/AK-01600 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: HEMODIALYSIS KIT: 2-LUMEN 12 FR X 16 CM/AK-12122-F recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PI JACC KIT: 2L 5.5 FR X 15 CM CG+/ASK-41552-LTAC recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PI PICC: 3: 6FR x 55CM w CHG/ DLX-35563-HPKC recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ARTERIAL LINE KIT: SL 20 GA X 5 IN/ASK-04510-MM6 RA CATH KIT: 20 GA X... recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: CVC/PSI KIT: 2 LUMEN 8 FR X 6 IN/ASK-42802-PLH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PI CVC KIT: 3L 7 FR X 16 CM AGB+/ASK-42703-PNHS2 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: AHDC KIT: 3-L 12 FR X 16 CM/AK-12123-PCDC recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: HEMODIALYSIS KIT: 2-LUMEN 8 FR X 11 CM/AK-11802-F recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: HEMODIALYSIS KIT: 2L 14 FR X 20 CM AGB CDC-25142-X1A recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: EPIDURAL CATHETER KIT: 19 GA X 90 CM/ASK-05502-VM1 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PI AGBA PICC KIT: 3L 6 FR X 40 CM W/VPS/ASK-44063-NS AGBA... recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PSI KIT: 7 FR X 4IN ANTIMICROBIAL/ASK-09701-UMH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: RA CATH KIT: 20 GA X 1 3/4 IN/TJ-04020-1 recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: AGBA PICC G4 Stylet: 3L 6FR x 55CM BP/DLX-45563-VPSB recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: PACING PSI KIT: 6 FR/AI-06210-KS recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: BIOPSY SYSTEM COMPREHENSIVE KIT/ASK-09458-AH recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - Description/REF: ACCESS TRAY/ASK-04001-SUH-S recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - PARACENTESIS KIT recall (ARROW INTERNATIONAL, LLC)
Medical deviceClass IReported June 24, 2026 · Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality... - DRAGONFLY Thai Ginger Powder Net Weight: 4.37 oz recall (U.S. Tov, Inc. dba U.S. Trading Company)
FoodClass IIReported June 17, 2026 · Potential contamination with lead. - EXCOR Pediatric Ventricular Assist Device recall (BERLIN HEART GMBH)
Medical deviceClass IIReported June 17, 2026 · Blood pump inner package expiration date does not match the outer-correct expiration date, which may lead to delays in surgical procedures. - Allia Moveo angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Allia IGS Pulse angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Allia IGS 7 Pulse angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Allia IGS 5 Pulse angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Allia IGS 3 Pulse angiographic X-ray system recall (GE Medical Systems, LLC)
Medical deviceClass IIReported June 17, 2026 · GE HealthCare has become aware of a potential issue affecting an electrical cable on certain IGS systems equipped with Gaia generators. This issue could lead... - Plum Duo Precision IV Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and... - Plum Duo Infusion Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and... - Plum Solo Precision IV Pump recall (ICU Medical, Inc.)
Medical deviceClass IIReported June 17, 2026 · Under certain conditions, the pump may not display a soft limit alert, and will not notify the clinician of a soft limit violation before confirming and... - Brand Name: Exacta Mix Product Name: Vented Micro-Volume Inlet Model/Catalog Number:... recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported June 10, 2026 · Affected lots may contain incorrect 0.8-micron filters. Use of a 0.8-micron filter in place of the validated 3-micron filter may lead to reduced flow... - Pediatric care bed recall (KAYSERBETTEN GMBH & CO. KG)
Medical deviceClass IReported June 10, 2026 · If the adjustment functions of the hand control, as instructed in the Manual, are not locked with the provided key when the patient (child) is unattended... - Wyze Labs Recalls Solar Cam Pan Security Cameras Due to Risk of Serious Injury from Fire and Burn Hazards
Consumer productReported June 5, 2026 · The recalled Wyze Solar Cam Pan security cameras' incorrect assembly instructions can lead consumers to accidentally puncture the lithium ion battery's metal... - Allura system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported June 3, 2026 · It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of... - Azurion system recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported June 3, 2026 · It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of... - Automated Impella Controller recall (Abiomed, Inc.)
Medical deviceClass IReported June 3, 2026 · A retrospective review identified that there are AIC units requiring specific hardware updates to address potential safety concerns. These hardware updates... - Liposomal Sleep Spray. Dosage: 6 sprays Liquid. Packaging: Aluminum bottle. 30 ml.... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml. Firm... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal D3+B12 Spray. Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml.... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal D3-5000IU Spray Dosage: 3 sprays Liquid. Packaging: Aluminum bottle. 30 ml.... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Prenatal+Postnatal Liquid Multivitamin Drops - Iron Free. Dosage: 3mL... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Women's Liquid Multivitamin Drops - Iron Free. Dosage: 3ml Liquid.... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Kids Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Collagen Booster. Dosage: 3mL Liquid. Packaging: Aluminum bottle. 90 ml.... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Women's Liquid Multivitamin Drops with Iron. Dosage: 3mL Liquid. Packaging:... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Mens 50+ Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Mens Liquid Multivitamin Drops. Dosage: 3mL Liquid. Packaging: Aluminum... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns. - Liposomal Womens 50+ Liquid Multivitamin Drops. Dosage: 3ml Liquid. Packaging:... recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen and possible C. Botulinum concerns.