Lead recalls (page 3)
349 recalls.
- FulviLife Complex. Dosage:2 tablespoons 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. - Joint Nourish. Dosage:2 tablespoons recall (Wellnov Supplements LLC)
FoodClass IIReported May 27, 2026 · Deviations from current Good Manufacturing Practices (cGMP) that could lead to bacterial pathogen contamination and possible C. Botulinum concerns. - OneLIF Interbody Cage recall (Novapproach Spine, LLC)
Medical deviceClass IIReported May 27, 2026 · Intervertebral body fusion system straight inserter failed to properly attach to affected cages, which may result in an inability to securely engage the... - Swan-Ganz Pacing Catheter recall (Becton, Dickinson and Company)
Medical deviceClass IIReported May 27, 2026 · Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection... - Swan-Ganz Jr Catheter recall (Becton, Dickinson and Company)
Medical deviceClass IIReported May 27, 2026 · Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection... - Swan-Ganz Catheter recall (Becton, Dickinson and Company)
Medical deviceClass IIReported May 27, 2026 · Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection... - LVIS Intraluminal Support Device recall (MICROVENTION INC.)
Medical deviceClass IIReported May 20, 2026 · Stent-assisted coiling device may due to commingling during manufacturing have dimensional nonconformance and/or incorrect device configuration. If device is... - NAPROXEN ORAL SUSPENSION recall (Acella Pharmaceuticals, LLC)
DrugClass IIReported May 13, 2026 · Chemical contamination; presence of lead and lithium above specification - ERBEFLO 2 recall (Erbe Medical, LLC)
Medical deviceClass IIReported May 13, 2026 · Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible... - ERBEFLO CleverCap: Hybrid Tubing/Cap Set for Olympus Scopes recall (Erbe Medical, LLC)
Medical deviceClass IIReported May 13, 2026 · Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible... - ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources recall (Erbe Medical, LLC)
Medical deviceClass IIReported May 13, 2026 · Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible... - VOCSN V+Pro package recall (Ventec Life Systems, Inc.)
Medical deviceClass IReported May 13, 2026 · Respiratory system intended to provide continuous/intermittent ventilator support, may not have been evaluated under all intended high-pressure conditions... - epoc BGEM BUN Test Card recall (Siemens Healthcare Diagnostics Inc)
Medical deviceClass IIReported May 6, 2026 · Use of the affected product can result in discrepant low pH and measured Total Carbon Dioxide (mTCO2) results and corresponding calculated values in arterial... - Dimension Creatinine Flex reagent cartridge. Material Number: 10872079. recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported May 6, 2026 · Siemens Healthcare Diagnostics is recalling certain lots of Dimension Creatinine Flex reagent cartridge (Dimension CRE2) because a potential imprecision in the... - AIDBAGs are first aid kits of convenience composed of individually labeled devices... recall (North American Rescue LLC.)
Medical deviceClass IReported May 6, 2026 · Kits contain the McKesson TRUE Metrix PRO Professional Monitoring Blood Glucose System that has been recalled for an issue with the software design of the E-5... - Brand Name: Disposable Mixing Bowls with Spatula Product Name: Mixing Bowl and... recall (Zimmer, Inc.)
Medical deviceClass IIReported May 6, 2026 · Ten complaints have been received identifying issues at the time of use related to the package seal, including incomplete seals, wrinkles in the seals or... - LeadCare Ultra Blood Lead Test Kit recall (Magellan Diagnostics, Inc.)
Medical deviceClass IIReported April 29, 2026 · Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing... - LeadCare¿ Plus Blood Lead Test Kit recall (Magellan Diagnostics, Inc.)
Medical deviceClass IIReported April 29, 2026 · Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing... - (1)(2) LeadCare¿ II Blood Lead Test Kit, (3)LeadCare¿ II 5X Blood Lead Test Kit, recall (Magellan Diagnostics, Inc.)
Medical deviceClass IIReported April 29, 2026 · Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing... - Omnipod 5 Pods. Model/Catalog number: PT-001662 ASM 5PK Pod STRL OPS G6G7 recall (Insulet Corporation)
Medical deviceClass IReported April 22, 2026 · Due to a manufacturing defect, certain Omnipod 5 Pods from 49 lots have an internal soft cannula tear that results in insulin leaking into the Pod instead of... - Multi-parameter Command Module recall (Spacelabs Healthcare, Inc.)
Medical deviceClass IIReported April 15, 2026 · Multi-parameter command module has a circuit board issue and when in Auto mode, Cardiac Output (CO) measurement may activate early, resulting in Bad Curve... - XTANT MEDICAL Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm recall (XTANT Medical Holdings, Inc)
Medical deviceClass IIReported April 15, 2026 · Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is. - Medline Kits containing ENFIT G-TUBE CONNECTOR 1. SKU DYKM2720 G/J TUBE CARE KIT ... recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage.... - ENFIT G-TUBE CONNECTOR recall (Medline Industries, LP)
Medical deviceClass IIReported April 8, 2026 · Connectors were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices, which could lead to leakage.... - Atellica CH Enzymatic Hemoglobin A1c recall (Siemens Healthcare Diagnostics, Inc.)
Medical deviceClass IIReported April 8, 2026 · A potential for depressed results for Atellica CH A1c_E when processing Atellica CH RCRP on the same analyzer. Customers processing A1c_E and RCRP on separate... - Imactis CT-Navigation System recall (GE Medical Systems, LLC)
Medical deviceClass IIReported April 1, 2026 · There is a potential issue that can lead to discordance between the simulated needle trajectory/tip position and the actual needle trajectory/tip position. - Specialized Bicycle Components Recalls Specialized Turbo Como SL Electric Bicycles Due to Risk of Serious Injury or Death from Fall Hazard
Consumer productReported March 19, 2026 · The bike's fork steerer tube can develop a small fatigue crack that can lead to a progressive failure of the fork, posing a fall hazard. - CHEMISTRY ANALYZER AU5800 recall (Beckman Coulter Mishima K.K.)
Medical deviceClass IIReported March 18, 2026 · A delay in results may occur. When clinical chemistry analyzer calibration monitor with PC installed with Microsoft SQL Server 2022 Express is open beyond15... - DxC 700 AU recall (Beckman Coulter Mishima K.K.)
Medical deviceClass IIReported March 18, 2026 · A delay in results may occur. When clinical chemistry analyzer calibration monitor with PC installed with Microsoft SQL Server 2022 Express is open beyond15... - Owner's Booklets and Instructions for Use that are used with the following blood... recall (Trividia Health, Inc.)
Medical deviceClass IReported March 18, 2026 · The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code... - Owner's Booklets and Instructions for Use that are used with the following blood... recall (Trividia Health, Inc.)
Medical deviceClass IReported March 18, 2026 · The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code... - Owner's Booklets and Instructions for Use that are used with the following blood... recall (Trividia Health, Inc.)
Medical deviceClass IReported March 18, 2026 · The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code... - Owner's Booklets and Instructions for Use that are used with the following blood... recall (Trividia Health, Inc.)
Medical deviceClass IReported March 18, 2026 · The system labeling (user manual and online labeling) did not provide adequate directions for lay users to act on the E-5 error code. The error code... - IBA Proton Therapy System - PROTEUS 235 recall (Ion Beam Applications S.A.)
Medical deviceClass IIReported March 18, 2026 · It was identified that eh Universal Beam Triggering Interface (UBTI) is disabled in the Therapy Safety System (TSS) configuration. In this condition, the TSS... - cobas pro integrated solutions with cobas c 503 analytical units: cobas pro sample... recall (Roche Diagnostics Operations, Inc.)
Medical deviceClass IIReported March 11, 2026 · Software defect, which allows the system to accept erroneous, non-monotonous calibrations for Spline-type assays. Cobas pro integrated solutions is an... - TheKiddoSpace Recalls Children's Christmas Tree Play Sets Due to Risk of Injury from Lead Exposure; Violates Federal Lead Content Ban and Mandatory Standard for Toys
Consumer productReported February 27, 2026 · The zipper pull on the music box compartment of the recalled Christmas Tree Toys contain levels of lead that exceed the federal lead content ban. Lead is toxic... - TheKiddoSpace Recalls Children's Flashcard Talking Toys Due to Risk of Injury from Lead and Phthalate Exposure; Violates Federal Lead Content and Phthalates Bans and Standard for Toys
Consumer productReported February 27, 2026 · The recalled children's flashcard toy sets contain levels of lead that exceed the federal lead content ban and levels of phthalates that exceed the federal... - TheKiddoSpace Recalls Children's Handwriting Practice Kits Due to Risk of Injury from Lead Exposure; Violates Federal Lead Content Ban
Consumer productReported February 27, 2026 · The pens in the recalled children's handwriting kits contain levels of lead in the nib that exceed the federal lead content ban. Lead is toxic if ingested by... - Brass Pital Pot 4-quart. Sticker label: BRASS HAMMERED HANDI NO 3 recall (Lotus Mom Corporation dba Indian Kitchen Mart)
FoodClass IReported February 25, 2026 · Potential contamination with leachable lead. - Aluminum Kadai with Metal Handles Size 5. A-Cook MADE IN INDIA SIZE 5 Sticker label:... recall (Lotus Mom Corporation dba Indian Kitchen Mart)
FoodClass IIReported February 25, 2026 · Potential contamination with leachable lead. - Brass Tope. Sticker label: $29.99+TAX recall (Lotus Mom Corporation dba Indian Kitchen Mart)
FoodClass IIReported February 25, 2026 · Potential contamination with leachable lead. - IKM Aluminum Saucepan 9" with Wooden Handle. Sticker label: ALUMINIUM PAN 2 SIDE... recall (Lotus Mom Corporation dba Indian Kitchen Mart)
FoodClass IIReported February 25, 2026 · Potential contamination with leachable lead. - MONARCH Platform recall (Auris Health, Inc)
Medical deviceClass IIReported February 25, 2026 · Device for bronchoscopic visualization, patient airway access has software issue: if application restarts after patient-side selection, prior to bronchoscope... - Private Label CVS. Model Number: CVS405406. Helps maintain a moist wound environment recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported February 25, 2026 · Potential packaging failures, which could lead to a breach in the sterile barrier. - MEDIHONEY CALCIUM ALGINATE WITH ACTIVE LEPTOSPERMUM HONEY. Model Numbers: recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported February 25, 2026 · Potential packaging failures, which could lead to a breach in the sterile barrier. - MediHoney Gel with Active Leptospermum Honey. Model/Catalog Numbers: recall (Integra LifeSciences Corp. (NeuroSciences))
Medical deviceClass IIReported February 25, 2026 · Potential packaging failures, which could lead to a breach in the sterile barrier. - Olympus High Flow Insufflation Unit. Model Number: UHI-3. Used for insufflation of... recall (Olympus Corporation of the Americas)
Medical deviceClass IReported February 25, 2026 · Issue with software algorithm which may lead to overpressure events. - Olympus High Flow Insufflation Unit. Model/ Number: UHI-2. Used for insufflation... recall (Olympus Corporation of the Americas)
Medical deviceClass IReported February 25, 2026 · Issue with software algorithm which may lead to overpressure events. - Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of... recall (Olympus Corporation of the Americas)
Medical deviceClass IReported February 25, 2026 · Issue with software algorithm which may lead to overpressure events. - da Vinci 5 Surgeon Console Viewer Display recall (Intuitive Surgical, Inc.)
Medical deviceClass IIReported February 18, 2026 · Robotic-assisted surgical system has Viewer Display manufactured with outdated firmware, may result in loss of one display-loss of 3D surgical field (depth... - Reprocessed Siemens ACUSON AcuNav Diagnostic Ultrasound Catheters: ACUSON AcuNav... recall (Medline Industries, LP)
Medical deviceClass IReported February 18, 2026 · These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response... - Reprocessed Biosense Webster SOUNDSTAR eco Diagnostic Ultrasound Catheters: ... recall (Medline Industries, LP)
Medical deviceClass IReported February 18, 2026 · These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response... - Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE Catheter... recall (Medline Industries, LP)
Medical deviceClass IReported February 18, 2026 · These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response... - Reprocessed St. Jude Supreme and Response Diagnostic Electrophysiology Catheters: ... recall (Medline Industries, LP)
Medical deviceClass IReported February 18, 2026 · These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response... - Reprocessed Livewire Steerable Diagnostic Electrophysiology Catheters: Livewire... recall (Medline Industries, LP)
Medical deviceClass IReported February 18, 2026 · These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response... - Reprocessed Abbott Inquiry Steerable Diagnostic Catheters: Abbott Inquiry... recall (Medline Industries, LP)
Medical deviceClass IReported February 18, 2026 · These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response... - Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter 10 Electrodes... recall (Medline Industries, LP)
Medical deviceClass IReported February 18, 2026 · These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response... - CINNAMON POWDER recall (VENZU TRADERS LLC)
FoodClass IIReported February 11, 2026 · Potential contamination with heavy metal (lead). - Rheumacare capsules recall (HANDELNINE GLOBAL LLC)
DrugClass IReported February 11, 2026 · CGMP Deviations: product found to contain lead. - Brand Name: Molift Product Name: Molift 4-point sling bars recall (ETAC A/S)
Medical deviceClass IIReported February 11, 2026 · A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this... - Brand Name: Molift Product Name: Molift 2-point sling bars recall (ETAC A/S)
Medical deviceClass IIReported February 11, 2026 · A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this... - Brand Name: Molift Product Name: Molift Mover 300 Model/Catalog Numbers: recall (ETAC A/S)
Medical deviceClass IIReported February 11, 2026 · A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this... - Brand Name: Molift Product Name: Molift Mover 205 Model/Catalog Number: recall (ETAC A/S)
Medical deviceClass IIReported February 11, 2026 · A customer experienced that during assembly and load testing of the device, the bolt for mounting the lifting bar broke. Upon further investigation of this... - Bubble Sensor for 3/8" x 3/32" tubing recall (Maquet Cardiopulmonary Gmbh)
Medical deviceClass IIReported February 11, 2026 · Internal investigations have identified an issue with the durability of the connecting cable near the connection to the Venous Bubble Sensor. Excessive bending... - Vivoo Sodium Test recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Vivoo Vaginal pH Test recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Vivoo Protein Test recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Vivoo pH Test recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Exploro Highly Sensitive Male Fertility / Sperm Concentration Test recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Male Fertility Sperm Test for Home Use recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - S. Typhi/Para Typhi A Antigen recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Menopause Test Cassette recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - LH One Step Ovulation Test Device recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - The Girlfriend Doctor Dr. Anna Cabeca Keto-pH-Uric Acid Test Strips recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - LotFancy Urinary Tract Infection Urine recall (Changchun Wancheng Bio-Electron Co., Ltd.)
Medical deviceClass IIReported February 11, 2026 · Test strips and other tests including for near-patient testing, that require a 510(k) were distributed before they could be legally marketed to U.S. customers... - Vortex Surgical Lindsell Sutured IOL Marker recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Vortex Surgical 25GA Backflush recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Rumex Disposable Diamond Dusted ILM Elevator recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Vortex Surgical I2 Injection Kit recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Tecfen Retractable Membrane Polisher recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Vortex Surgical 25GA I.D.D. Internal Delivery Device recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. 25GA... recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - 25GA Subretinal Injection Cannula VS0220.25 recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Vortex Disposable Forceps and Cannula 1. 23GA ACTU8 Forceps Adaptive VS0740.23 ... recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Oertli 1. 23G Laser Probe OS4 Flex-Tip VK401113 2. 23G Laser Probe OS4... recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Vortex Surgical 1. 23GA Laser Probe Curved Cat No. VS0120.23 2. 25GA Laser... recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens recall (Vortex Surgical Inc.)
Medical deviceClass IIReported February 11, 2026 · There may be voids located in the seal of Tyvek pouches associated with identified catalog numbers and lots. A compromised sterile barrier has potential of... - VITEK 2 Gram-negative Susceptibility Cards Containing o Polymyxin B recall (Biomerieux Inc)
Medical deviceClass IIReported February 11, 2026 · Potential risk of Quality Control failures and/or false resistant antibiotic results when testing isolates of Enterobacterales/Enterobacteriaceae species... - CellMek SPS Sample Preparation System recall (Beckman Coulter, Inc.)
Medical deviceClass IIReported February 11, 2026 · Sample preparation system designed to automate staining, lysing, cell washing has a software error that causes samples to be dispensed close to or touching... - Chest Drainage Units and Accessories: Product Code Description 1.... recall (Cardinal Health 200, LLC)
Medical deviceClass IIReported February 4, 2026 · The firm is updating the IFU to clarify the intended patient population for the identified chest drainage units and accessories as adults, 18 years and older.... - SIGMA Spectrum Infusion Pump recall (Baxter Healthcare Corporation)
Medical deviceClass IIReported January 28, 2026 · Certain pumps have potentially been released from service with defective grease applied to the cam and motor gears. Due to its low viscosity, the defective... - DPA161 Shrimp Paste recall (GUSTO GROUP, INC.)
FoodClass IIReported January 21, 2026 · Product tested high for lead. - Shrimp Paste recall (GUSTO GROUP, INC.)
FoodClass IIReported January 21, 2026 · Product tested high for lead. - Portex Spinal Tray recall (ICU Medical Inc.)
Medical deviceClass IIReported January 21, 2026 · Affected lots of syringes may have a crack on the syringe collar, which may lead to delayed or repeated blood draw/fluid delivery. This issue may also lead to... - Pulsator Arterial Blood Sampling Kit recall (ICU Medical Inc.)
Medical deviceClass IIReported January 21, 2026 · Affected lots of syringes may have a crack on the syringe collar, which may lead to delayed or repeated blood draw/fluid delivery. This issue may also lead to... - Brand Name: PALACOS Product Name: PALACOS MV pro 40 recall (Heraeus Medical GmbH (Dental Division))
Medical deviceClass IIReported January 21, 2026 · increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an... - Brand Name: PALACOS Product Name: PALACOS MV+G pro 40 recall (Heraeus Medical GmbH (Dental Division))
Medical deviceClass IIReported January 21, 2026 · increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an... - Brand Name: PALACOS Product Name: PALACOS R+G pro 40 recall (Heraeus Medical GmbH (Dental Division))
Medical deviceClass IIReported January 21, 2026 · increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an... - Brand Name: PALACOS Product Name: PALACOS R pro 40 recall (Heraeus Medical GmbH (Dental Division))
Medical deviceClass IIReported January 21, 2026 · increase of complaints regarding the breakage of the ampoules within their device systems. An extensive investigation revealed that multiple factors have an... - Allura Xper FD20/20 recall (PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.)
Medical deviceClass IIReported January 21, 2026 · Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections...