Health & Personal Care
HIGH
FDA DRUG
Viona Pharmaceuticals Recalls Tavaborole Topical Solution 5% Over Discoloration (2025)
TAVABOROLE
Discoloration
choking hazard Recalls
233 recalls tagged with “choking hazard”.
Food & Beverages
HIGH
FDA FOOD
Baker's Authority Everything Bagel Mix Recall Affects 197 Units for Sesame Allergy Risk
Product label does not list ingredients including major food allergen: sesame. Additional undeclared ingredients include: poppy seeds, dried garlic, dried onion, and sea salt
Baker's Authority
Product label
Food & Beverages
HIGH
FDA FOOD
Baker's Authority Recalls 78 Units of Three Seed Mix for Sesame Allergen (2025)
Product label does not list ingredients including major food allergen: sesame. Additional undeclared ingredients include: millet and flax
Baker's Authority
Product label
Health & Personal Care
HIGH
FDA DRUG
Glenmark Theophylline Extended-Release 400mg Recall Expanded for Failed Dissolution Tests (2025)
Glenmark Pharmaceuticals Inc.
Failed Dissolution
Health & Personal Care
HIGH
FDA DEVICE
Schiller Argus PB-3000 Vital Signs Monitor Recall Affects 266 US Units
Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the high-pressure range.
Schiller
Vital sign
HIGH
HIGH
CPSC
TEMI Go Basketball Toy Recalled for Choking Hazard Sold on Amazon (2025)
TEMI Go Basketball Toys
The recalled
Health & Personal Care
HIGH
FDA DRUG
Glenmark Carvedilol 25 mg Recall for Nitrosamine Impurity Affects 4,800 Bottles (2025)
CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity above the current Acceptable Intake Level.
Glenmark Pharmaceuticals
CGMP Deviations:
HIGH
CPSC
AliExpress Recalls LeymanKids Children's Pajama Sets for Burn Risk in 2025 Recall
AliExpress
The recalled
Health & Personal Care
HIGH
FDA DRUG
Westminster Pharmaceuticals Metoprolol Tartrate 100 mg Recalled for Nitrosamine Above ADI Level (202
CGMP Deviations: Presence of a nitrosamine, N-nitroso-metoprolol above the established Acceptable Daily Intake (ADI) level.
Metoprolol Tartrate
CGMP Deviations:
Health & Personal Care
HIGH
FDA DRUG
Glenmark Carvedilol 25 mg Recall Expands Over NNCI Impurity Above FDA Limit in 14,976 Bottles
CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity observed to be above the FDA-recommended limit of NMT 4.0 ppm
CARVEDILOL
CGMP Deviations:
Health & Personal Care
HIGH
FDA DEVICE
Tandem Diabetes Care Recalls 122,958 t:slim X2 and Tandem Mobi Pumps Over Autobolus Risk (2025)
Tandem Diabetes Care
A software
Health & Personal Care
HIGH
FDA DRUG
Hospira Epinephrine Injection Vials Recalled for Lack of Sterility Assurance (2025)
Lack of Assurance of Sterility.
Epinephrine
Lack of
Food & Beverages
HIGH
FDA FOOD
DFA Dairy Brands Frozen Dessert Recalled for Undeclared Wheat and Soy, 324 Containers Affected
Product contains undeclared wheat and soy.
DFA Dairy Brands
Product contains
MEDIUM
MEDIUM
CPSC
IKEA 365+ VARDEFULL Garlic Press Recalled for Laceration and Ingestion Hazards (2025)
IKEA
Small metal
Health & Personal Care
HIGH
FDA DEVICE
Medline Recalled 7,913 Reprocessed Webster CS Catheters for Electrophysiology Mapping
Medline Industries, LP
Specific lots
Health & Personal Care
HIGH
FDA DRUG
Pfizer Levoxyl Recall: Subpotent Levoxyl 50 mcg Tablets, 29,004 Bottles in U.S. Market (2025)
Pfizer's Levoxyl 50 mcg levothyroxine tablets are recalled due to subpotency. About 29,004 bottles distributed in the U.S. since distribution. Consumers should stop use and contact their healthcare provider for guidance.
Levoxyl
Subpotent drug
Health & Personal Care
HIGH
FDA DRUG
Quallent Duloxetine Delayed-Release Capsules 60 mg Recall Expanded for Impurity Above FDA Interim Lm
CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.
DULOXETINE
CGMP Deviations:
HIGH
CPSC
Minongad LED Gloves ST01 Recalled for Battery Ingestion Hazard Sold on Amazon (2025)
LED Gloves
The recalled