FoodFeb 12, 2025
Monkey Spit 12 fl oz recall — FDA F-0460-2025
Barbeque sauce product contains undeclared listing of (Milk) in product ingredient listing from sub-ingredient Butter.
Class IIFDA: TerminatedMonkey Spit
February 2025 recalls — page 9
These records include useful source details for the selected month.
FoodFeb 12, 2025
Monkey Spit 12 fl oz recall — FDA F-0459-2025
Barbeque sauce product contains undeclared allergen listing of (Milk) in product ingredient listing from sub-ingredient Butter.
Class IIFDA: TerminatedMonkey Spit
FoodFeb 12, 2025
Vidaslim Co Root Plus, and Root Capsules), VidaSlim 30-day recall — FDA F-0468-2025
Due to the presence of Toxic yellow oleander
Class IFDA: OngoingVidaslim Co.
FoodFeb 12, 2025
Bazzini NuGo Dark Chocolate Pretzel with Sea Salt , Real Dark recall — FDA F-0461-2025
The product is being recalled because of undeclared milk .
Class IFDA: TerminatedBazzini LLC
FoodFeb 12, 2025
Bazzini NuGo Dark Pretzel/Chocolate Chip Multipack 18 ct., 50g bar, 18 recall — FDA F-0463-2025
The product is being recalled because of undeclared milk .
Class IFDA: TerminatedBazzini LLC
FoodFeb 12, 2025
La Fiesta Food Products NET WT 8 OZ recall — FDA F-0532-2025
Firm distributed a Bread Crumb product with undeclared allergen (Sesame) not on the label.
Class IFDA: TerminatedLa Fiesta Food Products
FoodFeb 12, 2025
La Fiesta Food Products NET WT 8 OZ recall — FDA F-0533-2025
Firm distributed a Seasoned Bread Crumb product with undeclared allergen (Sesame) not on the label.
Class IFDA: TerminatedLa Fiesta Food Products
FoodFeb 12, 2025
Atkinson Milling Company ATKINSON'S NO ONIONS PLAIN NO ONIONS HUSHPUPPIES NET WT recall — FDA F-0467-2025
Undeclared Milk. During the firm's reordering process of labels, they discovered that the label does not list milk in its ingredient or contain statement.
Class IFDA: CompletedAtkinson Milling Company
VehicleFeb 12, 2025
Volkswagen Group of back over prevention software recall — NHTSA campaign 25V082000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2022-2024 Tiguan, 2023 Arteon, and 2024-2025 Audi Q3 vehicles. An error may occur in the camera control unit at vehicle…
back over prevention softwareVolkswagen Group of America, Inc.
DrugFeb 12, 2025
Timolol Maleate Ophthalmic Solution USP, 0.5%, Sterile, 5mL bottles recall — FDA D-0214-2025
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
DrugFeb 12, 2025
ENDO USA Adrenalin Chloride Solution recall — FDA D-0223-2025
Labeling: Not Elsewhere Classified: misleading label similar in appearance to the FDA-approved drug product Adrenalin (epinephrine injection, USP)
Class IFDA: OngoingENDO USA, Inc.
DrugFeb 12, 2025
Granix (tbo-filgrastim) Injection 300 mcg/0.5 mL, Single Dose prefilled syringe, packaged as recall — FDA D-0218-2025
Failed Stability Specifications - 12-month stability test result for one of the known peptides is below the specification limit
Class IIFDA: OngoingTeva Pharmaceuticals USA, Inc
DrugFeb 12, 2025
Potassium Chloride Extended-Release Tablets, USP, 10 mEq (750 mg), 100 Tablets per carton recall — FDA D-0221-2025
Failed Dissolution Specifications.
Class IIFDA: OngoingThe Harvard Drug Group LLC dba Major Pharmaceuticals…
DrugFeb 12, 2025
RemedyRepack Carvedilol 25 mg Tablet, QTY: 30 Tablets per Blister Pack recall — FDA D-0217-2025
CGMP deviations: presence of N-Nitroso Carvedilol Impurity-1 (NNC 1), above the FDA recommended acceptable intake limit.
Class IIFDA: TerminatedRemedyRepack Inc.
VehicleFeb 6, 2025
Toyota Motor Engineering & Manufacturing webbing recall — NHTSA campaign 25V059000
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2025 Toyota Camry Hybrid, Lexus NX250, NX350, NX350 Hybrid, 2024-2025 Lexus RX350, RX350 Hybrid, and RX500 Hybrid…
webbingToyota Motor Engineering & Manufacturing
VehicleFeb 6, 2025
Tacoma 4-wheel drive hoses, lines/piping, and fittings recall — NHTSA campaign 25V058000
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2024-2025 Tacoma 4-wheel drive vehicles. The rear brake hoses can be damaged if mud and dirt builds up inside the rear…
hoses, lines/piping, and fittingsToyota Motor Engineering & Manufacturing
VehicleFeb 6, 2025
GMC Sierra 1500 active shutters/grill recall — NHTSA campaign 25V060000
General Motors, LLC (GM) is recalling certain 2022 GMC Sierra 1500 vehicles equipped with chrome front grille deflectors. The attachments that hold the front grille deflectors in place may…
active shutters/grillGeneral Motors, LLC
Medical DeviceFeb 5, 2025
Boston Scientific AXIOS Stent and Electrocautery- Enhanced Delivery System 20mmx10mm UPN recall — FDA Z-1026-2025
Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the…
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceFeb 5, 2025
SenTiva DUO" VNS Therapy SenTiva DUO", Model 1000-D recall — FDA Z-1068-2025
Their is a potential that implanted pulse generators may stop delivering therapy due to an internal component issue.
Class IIFDA: OngoingLivaNova USA, Inc.
Medical DeviceFeb 5, 2025
muRata Vios Monitoring System Model 2050 recall — FDA Z-1069-2025
During the set-up and workflow to begin Vios monitoring, it has been noticed that patient vital signs and ECG waveforms can become distorted and will flicker or flash very fast. This issue…
Class IIFDA: OngoingMurata Vios, Inc.
Medical DeviceFeb 5, 2025
Medline procedure kits labeled as: 1) SHORT TERM INFUSAPORT ACCESS KIT, Reorder number recall — FDA Z-1041-2025
Certain Medline kits were manufactured and distributed with Procedure Masks with SO SOFT Earloops, and SOFT TOUCH II Surgical Masks which were subsequently recalled for not meeting the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceFeb 5, 2025
SenTiva" VNS Therapy" SenTiva", Model 1000 recall — FDA Z-1067-2025
Their is a potential that implanted pulse generators may stop delivering therapy due to an internal component issue.
Class IIFDA: OngoingLivaNova USA, Inc.
Medical DeviceFeb 5, 2025
Boston Scientific AXIOS Stent and Delivery System 15mmx10mm UPN: M00553750 recall — FDA Z-1031-2025
Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the…
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceFeb 5, 2025
Boston Scientific HOT AXIOS Stent and Electrocautery- Enhanced Delivery System 6mmx8mm UPN recall — FDA Z-1032-2025
Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the…
Class IIFDA: OngoingBoston Scientific Corporation
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.