FoodOct 9, 2024
Kent Precision Foods Group 1 recall — FDA F-0007-2025
Potential foreign material (metal)
Class IIFDA: TerminatedKent Precision Foods Group, Inc.
Latest records
Latest recalls — page 321
The newest recall records with useful source details are listed here.
FoodOct 9, 2024
Inner Waymark Heart of the Earth recall — FDA F-0004-2025
Elevated lead level 0.671 ppm in cacao (chocolate)
Class IIFDA: OngoingInner Waymark LLC
FoodOct 9, 2024
The Posh Bakery Whole Grains Bakery labeled "Lemon Muffin", 6 oz recall — FDA F-0019-2025
Undeclared whey (milk) & wheat flour; no nutrition fact panel & no contains statement
Class IIFDA: OngoingThe Posh Bakery, Inc.
FoodOct 9, 2024
Big Bottom Milk Company CHOCOLATE MILK GRADE A, 1 US Half Gallon recall — FDA F-0012-2025
Required pasteurization temperatures were not achieved.
Class IIFDA: OngoingBig Bottom Milk Company
FoodOct 9, 2024
Grace Imports KERALA MIXTURE INGREDIENTS: Gram Flour 48%, Edible Veg Oil recall — FDA F-0002-2025
Undeclared wheat. The firm was notified by their supplier that they failed to include the allergen "wheat" on the label.
Class IIFDA: OngoingGrace Imports, Inc.
FoodOct 9, 2024
The Posh Bakery Whole Grains Bakery labeled "Apple Cinnamon Muffin", 6 oz recall — FDA F-0015-2025
Undeclared whey (milk) & wheat flour: no nutrition fact panel & no contains statement
Class IIFDA: OngoingThe Posh Bakery, Inc.
FoodOct 9, 2024
Grace Imports SPICY MURUKKU INGREDIENTS: Rice Flour, Edible Veg Oil recall — FDA F-0003-2025
Undeclared wheat. The firm was notified by their supplier that they failed to include the allergen "wheat" on the label.
Class IIFDA: OngoingGrace Imports, Inc.
FoodOct 9, 2024
The Posh Bakery Whole Grains Bakery labeled "Banana Nut Muffin", 6 oz recall — FDA F-0020-2025
Undeclared whey (milk) and wheat flour; no nutritional fact panel & no contains statement
Class IIFDA: OngoingThe Posh Bakery, Inc.
FoodOct 9, 2024
The Posh Bakery Whole Grains Bakery labeled "Blueberry Muffin", 6 oz recall — FDA F-0018-2025
Undeclared whey (milk) & wheat flour: no nutrition fact panel & no contains statement
Class IIFDA: OngoingThe Posh Bakery, Inc.
FoodOct 9, 2024
Big Bottom Milk Company CHOCOLATE MILK GRADE A, 1 US Pint recall — FDA F-0013-2025
Required pasteurization temperatures were not achieved.
Class IIFDA: OngoingBig Bottom Milk Company
DrugOct 9, 2024
Supercore Products Group Hard Steel Capsules recall — FDA D-0003-2025
Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.
Class IFDA: OngoingSupercore Products Group Inc.
DrugOct 9, 2024
Ryaltris recall — FDA D-0006-2025
Defective Delivery System: The dip tube is clogged causing the spray not to work.
Class IIFDA: OngoingGlenmark Pharmaceuticals Inc., USA
DrugOct 9, 2024
Glenmark Pharmaceuticals Inc., USA Ciclopirox Gel 0.77%, For Dermatologic Use Only, Not for recall — FDA D-0002-2025
Defective Container: Firm received complaints of broken tube at the seal.
Class IIIFDA: OngoingGlenmark Pharmaceuticals Inc., USA
DrugOct 9, 2024
Atorvastatin Calcium Tablets, USP, 40mg recall — FDA D-0001-2025
Presence of Foreign Tablets/Capsules: A Carbamazepine Extended-Release 400 mg tablet was found in a 1000-count bottle of Atorvastatin Calcium Tablets, USP 40 mg.
Class IIFDA: TerminatedNivagen Pharmaceuticals Inc
DrugOct 9, 2024
Supercore Products Group Gold Hard Steel Plus Liquid, 2 FL OZ bottles, UPC 787188873199 recall — FDA D-0004-2025
Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.
Class IFDA: OngoingSupercore Products Group Inc.
VehicleOct 3, 2024
Nissan back over prevention recall — NHTSA campaign 24V748000
Nissan North America, Inc. (Nissan) is recalling certain 2024-2025 Rogue and 2025 INFINITI QX80 vehicles. A software error may cause the rearview camera to display a blank screen when the…
back over preventionNissan North America, Inc.
VehicleOct 3, 2024
Honda steering recall — NHTSA campaign 24V744000
Honda (American Honda Motor Co.) is recalling certain 2023-2025 Acura Integra, Civic Type R, CR-V Hybrid, CR-V, HR-V, 2022-2025 Civic, Civic Hatchback, 2024-2025 Acura Integra Type S, 2025…
steeringHonda (American Honda Motor Co.)
Medical DeviceOct 2, 2024
Boston Scientific AGILE ESO FC RMV 23MM X 10.1CM IN 18.5 F-Agile Esophageal Partially recall — FDA Z-3294-2024
WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire (OTW) Stent System due to the potential for delivery catheter tip detachment.
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceOct 2, 2024
Boston Scientific WALLFLEX PC ESOPH STENT 18/23MM X 103MM- Wallflex Esophageal Partially recall — FDA Z-3281-2024
WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire (OTW) Stent System due to the potential for delivery catheter tip detachment.
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceOct 2, 2024
American Contract Systems Open Shoulder, LWOS39L recall — FDA Z-3230-2024
ACS identified that due to an inoperable chart recorder, humidity readings were out-of-specification in one of the controlled environment areas. As a result, ACS is unable to confirm…
Class IIFDA: OngoingAmerican Contract Systems, Inc.
Medical DeviceOct 2, 2024
Hologic Selenia Dimensions/ 3Dimensions-Digital breast tomosynthesis Software Version recall — FDA Z-3248-2024
Identified an issue with Selenia Dimensions 1.12.0 and 3Dimensions 2.3.0 system software when used in combination with C-View software in which the quality of the final C-View synthesized…
Class IIFDA: OngoingHologic Inc.
Medical DeviceOct 2, 2024
Cook Biotech Biodesign Fistula Plug C-FPS-0.4 - For implantation to reinforce soft tissue recall — FDA Z-3253-2024
Products expire prior to the expiration date printed on the product labeling
Class IIFDA: OngoingCook Biotech, Inc.
Medical DeviceOct 2, 2024
Boston Scientific AGILE ESO OTW PC 23MM X 10.1CM IN 18.5 F-Agile Esophageal Partially recall — FDA Z-3288-2024
WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire (OTW) Stent System due to the potential for delivery catheter tip detachment.
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceOct 2, 2024
Karl Storz - Endoskope , REF: 27830KA, Nephroscope for MIP M, Rx only, CE 0123 recall — FDA Z-3224-2024
Various medical device product IFUs contain reprocessing modalities that have not been reviewed and/or approved for safety and efficacy by the FDA.
Class IIFDA: OngoingKarl Storz Endoscopy
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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