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.
October 2024 recalls — page 12
These records include useful source details for the selected month.
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
Medical DeviceOct 2, 2024
Wipro GE Healthcare Private GE Giraffe Warmer, Model/Catalog Number M1118179-01090979 recall — FDA Z-3080-2024
GE HealthCare has become aware that complete electrical safety testing was not conducted during manufacturing of certain Giraffe and Panda iRes Warmers. There are multiple electrical safety…
Class IIFDA: OngoingWipro GE Healthcare Private Ltd.
Medical DeviceOct 2, 2024
American Contract Systems Arthroscopy Pack, MSKA45A recall — FDA Z-3229-2024
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.
How to use this monthly recall archive
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.