FoodMar 26, 2025
Growland Dried Longan Pulp- Made in China, 8oz recall — FDA F-0648-2025
Elevated levels of Sulfites in Dried Longan Pulp
Class IIFDA: OngoingGrowland Inc.
Monthly breakdown
2025 recalls by month
Select a month to review the recall records reported during that period.
December 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categoriesSeptember 2025285 records · 4 categoriesAugust 2025239 records · 4 categoriesJuly 2025370 records · 4 categoriesJune 2025342 records · 4 categoriesMay 2025258 records · 4 categoriesApril 2025302 records · 4 categoriesMarch 2025259 records · 4 categoriesFebruary 2025260 records · 4 categoriesJanuary 2025354 records · 4 categories
2025 recalls — page 127
Records are ordered by the best available source date.
FoodMar 26, 2025
Lyons Magnus Ready Care Vanilla Shake No Sugar Added recall — FDA F-0659-2025
Potential contamination with Listeria monocytogenes.
Class IFDA: OngoingLyons Magnus LLC
FoodMar 26, 2025
Lyons Magnus Ready Care Chocolate Shake No Sugar Added recall — FDA F-0656-2025
Potential contamination with Listeria monocytogenes.
Class IFDA: OngoingLyons Magnus LLC
FoodMar 26, 2025
Great Lakes Cheese Co Happy Farms by ALDI Colby Jack recall — FDA F-0641-2025
Potential foreign material (stainless steel fragments)
Class IIFDA: TerminatedGreat Lakes Cheese Co Inc.
FoodMar 26, 2025
Lyons Magnus Ready Care Strawberry Shake recall — FDA F-0654-2025
Potential contamination with Listeria monocytogenes.
Class IFDA: OngoingLyons Magnus LLC
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
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
About the 2025 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.