FoodMar 26, 2025
Lyons Magnus Ready Care Strawberry Shake No Sugar Added recall — FDA F-0657-2025
Potential contamination with Listeria monocytogenes.
Class IFDA: OngoingLyons Magnus LLC
Latest records
Latest recalls — page 248
The newest recall records with useful source details are listed here.
DrugMar 26, 2025
Slate Run Pharmaceuticals Cinacalcet Hydrochloride Tablets 30 mg, 30-count bottle recall — FDA D-0278-2025
CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits.
Class IIFDA: CompletedSlate Run Pharmaceuticals
DrugMar 26, 2025
Levothyroxine Sodium Tablets, USP, 150 mcg (0.15 mg) recall — FDA D-0290-2025
Super-Potent Drug: Out of specification potency results were obtained.
Class IIFDA: OngoingMylan Institutional, Inc.
DrugMar 26, 2025
Neupogen (filgrastim) For Injection, 480 mcg/1.6 mL (300 mcg/1 mL), 1.6 mL single Dose Vial recall — FDA D-0286-2025
Stability data does not support expiry: the products have the potential to be out of specification at the time of expiry of 36-months.
Class IIFDA: OngoingAmgen, Inc.
DrugMar 26, 2025
Slate Run Pharmaceuticals Cinacalcet Hydrochloride Tablets 60 mg, 30-count bottle recall — FDA D-0279-2025
CGMP deviations: The presence of nitrosamine impurity above the acceptable daily intake limits.
Class IIFDA: CompletedSlate Run Pharmaceuticals
DrugMar 26, 2025
Levothyroxine Sodium Tablets, USP, 125 mcg (0.125 mg) recall — FDA D-0291-2025
Super-Potent Drug: Out of specification potency results were obtained.
Class IIFDA: OngoingMylan Institutional, Inc.
DrugMar 26, 2025
Ciprofloxacin Ophthalmic Solution USP, 0.3% as base, package in 5 mL bottles recall — FDA D-0282-2025
Defective container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle
Class IIFDA: OngoingFDC Limited
DrugMar 26, 2025
Neupogen (filgrastim) For Injection, 300mcg/1 mL, 1 mL Single Dose Vials recall — FDA D-0285-2025
Stability data does not support expiry: the products have the potential to be out of specification at the time of expiry of 36-months.
Class IIFDA: OngoingAmgen, Inc.
VehicleMar 24, 2025
Volvo Car USA electrical system software recall — NHTSA campaign 25V179000
Volvo Car USA, LLC (Volvo Car) is recalling certain 2020-2021 S90, 2020-2022 S60, V60, XC60, XC90, and 2022 V90 plug-in hybrid vehicles. The high-voltage battery may experience a short…
electrical system softwareVolvo Car USA, LLC
Medical DeviceMar 19, 2025
Aesculap Numerous models of nonsterile hemostatic forceps: (1) REF BH198R, Fuchsig Artery recall — FDA Z-1310-2025
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Class IIFDA: OngoingAesculap Inc.
Medical DeviceMar 19, 2025
GE Medical Systems GE Healthcare Revolution Apex Elite, System, X-ray, Tomography, Computed recall — FDA Z-1298-2025
GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in…
Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceMar 19, 2025
ZOLL Powerheart G5 AED recall — FDA Z-1323-2025
The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
Class IIFDA: OngoingZOLL Medical Corporation
Medical DeviceMar 19, 2025
GE Medical Systems GE Healthcare Revolution Apex Plus, System, X-ray, Tomography, Computed recall — FDA Z-1300-2025
GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in…
Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceMar 19, 2025
Aesculap Numerous models of nonsterile hemostatic forceps: (1) REF FB458R, Glover ATR.CLAMP recall — FDA Z-1311-2025
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Class IIFDA: OngoingAesculap Inc.
Medical DeviceMar 19, 2025
GE Medical Systems GE Healthcare Revolution Apex Expert, System, X-ray, Tomography, Computed recall — FDA Z-1299-2025
GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in…
Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceMar 19, 2025
CareFusion 303 BD Care Coordination Engine (CCE) Infusion Adapter, Safety Management recall — FDA Z-1305-2025
Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU).
Class IFDA: OngoingCareFusion 303, Inc.
Medical DeviceMar 19, 2025
Quantum Perfusion Centrifugal Blood Pump CP22 with Integrated Sensors Pump, Blood recall — FDA Z-1327-2025
Their is a potential of fluid leakage from the centrifugal blood pump pump during the priming procedure or during clinical procedures.
Class IIFDA: OngoingSpectrum Medical Inc.
Medical DeviceMar 19, 2025
GE Medical Systems GE Healthcare Revolution CT ES, System, X-ray, Tomography, Computed recall — FDA Z-1303-2025
GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in…
Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceMar 19, 2025
ZOLL Powerheart G5 AED recall — FDA Z-1318-2025
The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
Class IIFDA: OngoingZOLL Medical Corporation
Medical DeviceMar 19, 2025
GE Medical Systems GE Healthcare Revolution CT, System, X-ray, Tomography, Computed recall — FDA Z-1302-2025
GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in…
Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceMar 19, 2025
Da Vinci 5 ASSY,DV5 CONSOLE,IS5000 Foot Tray Pedals recall — FDA Z-1325-2025
Due to an increase in complaints concerning foot tray pedal spring failing resulting in the pedal remaining pressed
Class IIFDA: OngoingIntuitive Surgical, Inc.
Medical DeviceMar 19, 2025
GE Medical Systems GE Healthcare Revolution Apex Select, System, X-ray, Tomography, Computed recall — FDA Z-1301-2025
GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in…
Class IIFDA: OngoingGE Medical Systems, LLC
Medical DeviceMar 19, 2025
Aesculap Numerous models of nonsterile hemostatic forceps: (1) REF BH100R, Carrel Artery recall — FDA Z-1309-2025
The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
Class IIFDA: OngoingAesculap Inc.
Medical DeviceMar 19, 2025
Smiths Medical ASD Portex Endotracheal Tube, Item Codes 100/105/025 100/105/030 100/105/035 recall — FDA Z-1289-2025
Affected devices have a smaller diameter than expected and may potentially result in inadequate ventilation to the patient. Patient may experience hypoxia, underdose, or cardiopulmonary…
Class IFDA: OngoingSmiths Medical ASD, Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 2026363 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories