Complete FDA and NHTSA recall records dated in 2024, organized for browsing by month, category and recalling company.
Select a month to review the recall records reported during that period.
Records are ordered by the best available source date.
Undeclared walnut and wheat. Mini Squash Harvest Loaf (UPC 8 55324 00505 3) was mis-labeled as Mini Raspberry Lemon Coffee Cake (UPC 8 57297 00745 4) and therefore wheat flour and walnuts…
Undeclared whey (milk), wheat flour, & bran (wheat); no nutrition fact panel & no contains statement
Undeclared whey (milk), wheat flour, & coconut; no nutrition fact panel & no contains statement
Eggs have the potential to be contaminated with Salmonella.
Potential foreign material (metal)
Acidified product was manufactured by firm without ODA license.
Potential foreign material (metal)
Elevated lead level 0.671 ppm in cacao (chocolate)
Undeclared whey (milk) & wheat flour; no nutrition fact panel & no contains statement
Required pasteurization temperatures were not achieved.
Undeclared wheat. The firm was notified by their supplier that they failed to include the allergen "wheat" on the label.
Undeclared whey (milk) & wheat flour: no nutrition fact panel & no contains statement
Undeclared wheat. The firm was notified by their supplier that they failed to include the allergen "wheat" on the label.
Undeclared whey (milk) and wheat flour; no nutritional fact panel & no contains statement
Undeclared whey (milk) & wheat flour: no nutrition fact panel & no contains statement
Required pasteurization temperatures were not achieved.
Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.
Defective Delivery System: The dip tube is clogged causing the spray not to work.
Defective Container: Firm received complaints of broken tube at the seal.
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.
Marketed without an approved NDA/ANDA: FDA analysis found products to be tainted with undeclared acetaminophen and sildenafil.
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…
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…
WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire (OTW) Stent System due to the potential for delivery catheter tip detachment.
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.
