Food & Beverages
HIGH
FDA FOOD
Sprout Organics 6+ Months Baby Food Recalled for Lead Contamination in 9,873 Cases (2025)
Potential contamination with heavy metal (Lead).
Sprout Organics
Potential contamination
stop use immediately Recalls
2,229 recalls tagged with “stop use immediately”.
Health & Personal Care
HIGH
FDA DRUG
Accord Healthcare Recalls 54,432 Levothyroxine 88 mcg Tablets for Subpotent Potency (2025)
Subpotent: During long term stability testing of Levothyroxine Sodium Tablets USP for 88 mcg, the assay content was observed below the approved specification range.
Levothyroxine Sodium
Subpotent: During
Food & Beverages
HIGH
FDA FOOD
Lawrence Wholesale Frozen Shrimp Recalled for Cs-137 Contamination (4,871 Cases, 2025)
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
Lawrence Wholesale
Product manufactured
Food & Beverages
HIGH
FDA FOOD
Lawrence Wholesale Shrimp Cocktail Bowls Recalled for Cs-137 Contamination Risk (2025)
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
Lawrence Wholesale
Product manufactured
Health & Personal Care
HIGH
FDA DEVICE
Abiomed Impella Automated Controller Recall Affects 9,177 Units Worldwide (2025)
Potential for Automated Impella Controller (AIC) purge pressure issues due to purge retainer failures.
Abiomed
Potential for
Health & Personal Care
HIGH
FDA DRUG
IntegraDose Oxytocin IV Solution Recall 2025 for Subpotent Drug, 853 Bags Nationwide
Subpotent Drug: Testing revealed there was no oxytocin in the IV bag.
IntegraDose Compounding Services
Subpotent Drug:
Health & Personal Care
HIGH
FDA DRUG
Carbamazepine Extended-Release 400 mg Tablets Recalled for Failed Dissolution Specifications (D-0675
Carbamazepine
Failed Dissolution
Health & Personal Care
HIGH
Health & Personal Care
HIGH
FDA DRUG
Graviti Pharmaceuticals Bupropion Hydrochloride XL 300 mg Recall Impacts 46,512 Bottles (2025)
Bupropion Hydrochloride
Failed Tablet/Capsule
Health & Personal Care
HIGH
FDA DRUG
Private Label Skin Care Inc. Benzoyl Peroxide Cleanser Recalled for Benzene Contamination (2025)
Private Label Skin Care Inc. recalled edunn clarity BP Treatment Cleanser 10% after benzene was detected. The recall covers lot numbers 58170A and 58172A with expiration September 2025. The product was distributed in California and Georgia.
Private Label Skin Care
Chemical Contamination:
Health & Personal Care
HIGH
FDA DRUG
Private Label Skin Care Micronized Benzoyl Peroxide Gel Recall Expands for Benzene Contamination
Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.
Private Label Skin Care
Chemical Contamination:
Health & Personal Care
HIGH
FDA DRUG
Skin MD Body Acne Cleanser Recalled for Elevated Benzene Levels (2025)
Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.
Skin MD
Chemical Contamination:
Health & Personal Care
HIGH
FDA DRUG
Torrey Pines Benzaderm BPO Cleanser 10% Recall Over Benzene Contamination, 2025
Torrey Pines Dermatology & Laser Center's Benzaderm BPO Cleanser recall remains active. The FDA-listed recall covers benzoyl peroxide cleanser lot numbers 58170A and 58172A with expiration 09/2025. Consumers should stop use and contact the recall coordinator.
Private Label Skin Care
Chemical Contamination:
Health & Personal Care
HIGH
FDA DRUG
Private Label Skin Care Inc. Benzoyl Peroxide 10% Acne Treatment Recalled for Benzene Contamination
Chemical Contamination: This recall has been initiated due to elevated levels of benzene that was discovered during post consume awareness with benzoyl peroxide products.
Private Label Skin Care
Chemical Contamination:
Health & Personal Care
HIGH
FDA DEVICE
UIH Technologies PET/CT System Recall Affects 3 Units Over Gantry Interference Risk (2025)
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
UIH Technologies
Third-party outer
Health & Personal Care
HIGH
FDA DRUG
Major Pharmaceuticals Chlorpromazine Hydrochloride 25 mg Tablets Recall 2025 for CGMP Deviations
CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake limit
Major Pharmaceuticals
CGMP Deviations:
Health & Personal Care
HIGH
FDA DRUG
Major Pharmaceuticals Chlorpromazine Hydrochloride 100 mg Recall 2025 — 866 Blister Packs Nationwide
CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake limit
Major Pharmaceuticals
CGMP Deviations:
Food & Beverages
HIGH
FDA FOOD
M.O.M Enterprises Recalls 46,752 Organic BABY Bedtime Drops Over Yeast Contamination (2025)
M.O.M Enterprises
Potential yeast
Health & Personal Care
HIGH
FDA DEVICE
Noah Medical Galaxy System GAL-001 Recall of 47 Units for Password-Protected Manual Access (2025)
Due to Users not having access to the Instructions for Use/User Manual due to it being password protected.
Noah Medical
Due to
Health & Personal Care
HIGH
FDA DEVICE
Argon Medical Devices Recalls 1,821 Option Elite IVC Filters for Dilator Resistance Risk (2025)
Due to complaints of increased resistance when advancing the dilator within the introducer sheath. This issue could potential result in procedural delays and/or risk of venous intimal injuries if excessive force is applied
Argon Medical Devices
Due to
Tag Statistics
Total Recalls
2,229