Recalls in May 2026 (page 2)
579 recalls.
- 1274108D PowerPICC SV Catheter 4 Fr Dual-Lumen REKW2449 00801741087110 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000662 PowerPICC SOLO HF Catheter 5 Fr Triple-Lumen UDI-DI Code: 00801741129674 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - 5625240 DuoGlide Short-Term Straight Dialysis Catheter 13 Fr Dual-Lumen UDI-DI Code:... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - CK000495A Poly Midline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741121609 ... recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - OTP5000 THORA/PARA TRAY recall (Bard Access Systems, Inc.)
Medical deviceClass IIReported July 8, 2026 · Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by... - RayCare 2024A SP4. Oncology Information Systems. recall (RAYSEARCH LABORATORIES AB)
Medical deviceClass IIReported July 8, 2026 · Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during... - RayCare 2024A SP1. Oncology Information Systems. recall (RAYSEARCH LABORATORIES AB)
Medical deviceClass IIReported July 8, 2026 · Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during... - ARTIS icono floor. Model Number: 11327700. recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported July 8, 2026 · Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits. - ARTIS icono ceiling. Model Number: 11328100. recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported July 8, 2026 · Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits. - ARTIS icono biplane. Model Number: 11327600. recall (Siemens Medical Solutions USA, Inc)
Medical deviceClass IIReported July 8, 2026 · Potential for loss of movement capability after adjusting the detector lift height to its maximum or minimum limits. - Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges recall (TELEFLEX LLC)
Medical deviceClass IIReported July 8, 2026 · Due to out-of-specification, or potential out-of-specification, levels of endotoxins - CRE Wireguided 18-20mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Wireguided 15-18mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Wireguided 12-15mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Wireguided 10-12mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Wireguided 8-10mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Wireguided 6-8mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 18-20mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 15-18mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 12-15mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 10-12mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 8-10mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - CRE Pro Wireguided 6-8mm 240cm recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 8, 2026 · Potential sterile breach of the pouches in which devices are packaged. - IntelliCuff recall (Hamilton Medical AG)
Medical deviceClass IIReported July 8, 2026 · Due to reported complaints, the cuff device may alarm with a "Cuff System Leakage" error. As a result, the motor may pump continuously and fail to maintain the... - Medtronic Harmony Delivery Catheter System recall (Medtronic Heart Valves Division)
Medical deviceClass IReported July 8, 2026 · Devices containing inner shaft assemblies from specific manufacturing lots may have an increased potential for distal tip detachment from the delivery system... - A M S recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IReported July 8, 2026 · Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a... - A M S recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IReported July 8, 2026 · Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a... - A M S recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IReported July 8, 2026 · Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a... - A M S recall (Windstone Medical Packaging, Inc.)
Medical deviceClass IReported July 8, 2026 · Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a... - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported July 8, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - Depuy Synthes recall (DEPUY (IRELAND))
Medical deviceClass IIReported July 8, 2026 · The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility. - 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... - Medline Convenience Kits: 1) OPHTHALMIC PACK W/LIDO recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) MERCY MEDICAL CIRCUMCISION TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) L&D CONTINUOUS EPIDURAL TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) LUMBAR PUNCTURE CHOICE recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) ARTERIAL LINE KIT recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) SUTURE TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) PI CVC KIT 3L 7 FR 16 CM recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) SUTURING SET recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) IMAGING BIOPSY TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) STD recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) DYNJ0621189X recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) MULTIMED recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) BLOCK TRAY recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) PAIN MGMT/ PREF W. MED NDL recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Medline Convenience Kits: 1) ARTERIAL ACCESS TRAY W/LIDOCAINE recall (Medline Industries, LP)
Medical deviceClass IIReported July 8, 2026 · The kits containing Huons Lidocaine HCL Injection USP 1% 10mg/ml 5mL Ampules (Lidocaine Ampules)(OEM). A recall notice was issued by Huons Co., Ltd. for... - Breathing circuit set recall (Hamilton Medical AG)
Medical deviceClass IReported July 8, 2026 · Ventilator coaxial breathing circuit may have, expiratory valve sets with membranes sticking to valve body, not detectable during pre-operative test, which... - boichik bagles Pumpernickel Mix Bagels 6 pre-sliced bagels recall (Boichik Bagels, Inc.)
FoodClass IIReported July 1, 2026 · Undeclared allergen, sesame. - boichik bagles Tuna Salad Ingredients: albacore tuna recall (Boichik Bagels, Inc.)
FoodClass IIReported July 1, 2026 · Ingredient statement declares eggs, but eggs are omitted from the "contains" allergen statement on the product labels. - boichik bagels Whitefish Salad Ingredients: Smoked whitefish recall (Boichik Bagels, Inc.)
FoodClass IIReported July 1, 2026 · Ingredient statement declares eggs, but eggs are omitted from the "contains" allergen statement on the product labels. - Pearl Milling Company Original Pancake & Waffle Mix Complete recall (CERELES EN GENERAL SAS)
FoodClass IReported July 1, 2026 · Undeclared allergens: Milk and Soy - Roast beef and cheddar closed face sandwich packed in clear plastic wrap with a green... recall (Produce Innovations)
FoodClass IIIReported July 1, 2026 · Incorrect Product Label; Roast Beef and Swiss closed face sub sandwich labeled as Turkey and Cheddar closed face sub sandwich - El David Gelee recall (Alb-USA Enterprises Inc)
FoodClass IIReported July 1, 2026 · Undeclared colors (FD&C Yellow 5 and FD&C Red 40). - Motor City Pizza Co. 5 Cheese Bread Single retail pack recall (Champion Foods, LLC)
FoodClass IIReported July 1, 2026 · potential salmonella contamination - BD ChloraPrep FREPP Clear recall (CareFusion 213, LLC)
DrugClass IReported July 1, 2026 · Non-Sterility: Due to presence of Aspergillus penicillioides. And Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the... - BD ChloraPrep Clear recall (CareFusion 213, LLC)
DrugClass IReported July 1, 2026 · Non-Sterility: Due to presence of Aspergillus penicillioides. - BD ChloraPrep FREPP Clear recall (CareFusion 213, LLC)
DrugClass IIReported July 1, 2026 · Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area. - BD ChloraPrep Clear recall (CareFusion 213, LLC)
DrugClass IIReported July 1, 2026 · Lack of Assurance of Sterility: Due to wrinkles in the paper lidding which may breach the seal area. - PReye Vitamin See Antioxidant Preservative Free Eye Drops recall (PReye LLC)
DrugClass IIReported July 1, 2026 · Lack of Assurance of Sterility - Fenofibrate Capsules recall (Ajanta Pharma USA Inc)
DrugClass IIReported July 1, 2026 · CGMP Deviations - Abiomed Impella CP Set with SmartAssist recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Abiomed Impella CP Set with SmartAssist recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Abiomed 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP. Impella Set Product... recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Abiomed 14 Fr x 13 cm Low Profile Introducer Kit for Impella CP. Impella Set Product... recall (Abiomed, Inc.)
Medical deviceClass IReported July 1, 2026 · Potential for thrombus formation during prolonged use of the introducer. - Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump recall (Boston Scientific Corporation)
Medical deviceClass IIReported July 1, 2026 · There is the potential for leakage along the drug pathway from the pump through the end of the catheter. - Brand Name: Persona Revision Product Name: Persona Revision¿ Trabecular Metal¿... recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Firm received a complaint with no clinical impact in which a posterior augment was found within the distal augment package. - Octopus 4 Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 1, 2026 · During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to... - Octopus Evolution AS Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 1, 2026 · During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to... - Octopus Evolution Tissue Stabilizer recall (Medtronic Perfusion Systems)
Medical deviceClass IIReported July 1, 2026 · During the manufacturing process, Medtronic personnel identified an assembly issue where the tubing was incorrectly positioned. The short tube was attached to... - Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 US... recall (Dexcom, Inc.)
Medical deviceClass IIReported July 1, 2026 · Certain lots of Dexcom G7 sensors originally designated as scrap and intended for destruction were stolen during the destruction process. The sensors were... - Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser. recall (IPG Medical Corporation)
Medical deviceClass IIReported July 1, 2026 · Software anomaly that causes a false display of error code 5018. - 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... - Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe... recall (Acumed LLC)
Medical deviceClass IIReported July 1, 2026 · Due to manufacturing error, hexalobe screws used with wrist fixation system may break during use. - Off-Axis Alliance Glenoid recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - Off-Axis Alliance Glenoid recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - Off-Axis Comprehensive Shoulder System recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - Off-Axis Comprehensive Shoulder System recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - Off-Axis Comprehensive Shoulder System Small recall (Zimmer, Inc.)
Medical deviceClass IIReported July 1, 2026 · Five complaints have been received identifying issues where the plastic guides were catching during reaming, leading to breakage. - VOCSN+Pro package recall (Ventec Life Systems, Inc.)
Medical deviceClass IIReported July 1, 2026 · Respiratory system intended to provide continuous/intermittent ventilator support, may have a damaged back-up battery supporting backup alarm function, which... - Philips Avalon Fetal Monitor recall (Philips North America Llc)
Medical deviceClass IIReported July 1, 2026 · Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or... - Philips Avalon Fetal Monitor recall (Philips North America Llc)
Medical deviceClass IIReported July 1, 2026 · Monitor has incorrect assembly of the speaker connector which can cause device cables to be pulled out of the housing and increase the risk of intermittent or... - Medline Convenience Kits: 1) DRAWER 6A ADULT CENTRAL LINE recall (Medline Industries, LP)
Medical deviceClass IReported July 1, 2026 · The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose... - Medline Convenience Kits: 1) DRAWER 6 CENTRAL LINE INSERTIO recall (Medline Industries, LP)
Medical deviceClass IReported July 1, 2026 · The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose... - Medline Convenience Kits: 1) OPEN HEART CDS recall (Medline Industries, LP)
Medical deviceClass IReported July 1, 2026 · The Medline Convenience Kits contain Arrow Kits and Sets that include Lidocaine Hydrochloride Injection, USP and Bupivacaine Hydrochloride in Dextrose...