Health & Personal Care
HIGH
FDA DRUG
Weh-Weh Pain Reliever Gel Recalled for CGMP Deviations, 810 Tubes Affected (2025)
WEH-WEH PAIN RELIEVER GEL
CGMP Deviations
immediate action Recalls
2,756 recalls tagged with “immediate action”.
Health & Personal Care
HIGH
FDA DRUG
Beauty4Pros Sunscreen Karina SPF 25 Recalled for CGMP Deviations (2025)
Beauty4Pros LLC recalls Karina Daily Moisturizer SPF 25 distributed to CA, CO, FL, PR, WA after CGMP deviations. 1,492 tubes affected. Stop use immediately and contact CA Botana International for guidance.
Sunscreen Karina Skin Care Moist
CGMP Deviations
Health & Personal Care
HIGH
FDA DRUG
Elixir by Coco March Tinted Mineral Sunscreen SPF 50 Recalled for CGMP Deviations
SUNSCREEN
CGMP Deviations
Health & Personal Care
HIGH
FDA DRUG
CLEARSTEM You Are Sunshine SPF 50 Sunscreen Recalled for CGMP Deviations (Visage)
CLEARSTEM
CGMP Deviations
Health & Personal Care
HIGH
FDA DRUG
CA Botana Mineral Sunscreen Recall Covers 1,167 Tubes Over CGMP Deviations (2025)
MINERAL SUNSCREEN
CGMP Deviations
HIGH
CPSC
Bellabu Bear Recalls Bamboo Sherpa Children's Robes for Burn Hazard (2025)
Bellabu Bear
The recalled
HIGH
CPSC
ESR HaloLock Wireless Power Banks Recalled in Expansion to Include 2G505 Model for Fire and Burn Haz
ESR HaloLock
The lithium-ion
Health & Personal Care
HIGH
FDA DRUG
Sucralfate Tablets Recalled by American Health Packaging for CGMP Deviations (27,868 Packs, 2025)
Sucralfate
CGMP Deviations:
Health & Personal Care
HIGH
FDA DRUG
STAQ Pharma FentaNYL Citrate PF IV Injection Recall 2025 Over Labeling Errors
STAQ Pharma recalled FentaNYL Citrate PF IV injection nationwide after labeling left incorrect or missing lot and expiration dates. Healthcare providers must stop using the product immediately. STAQ Pharma will provide recall instructions by letter.
STAQ Pharma
Labeling: Incorrect
Health & Personal Care
HIGH
FDA DRUG
STAQ Pharma Ketamine Hydrochloride Injection 50 mL Recall for Labeling Errors (2025)
Labeling: Incorrect or Missing Lot and/or Exp Date
STAQ Pharma
Labeling: Incorrect
HIGH
Health & Personal Care
HIGH
FDA DRUG
STAQ Pharma Hydromorphone HCl PF 10mg/50mL IV Injection Recall for Labeling Errors (2025)
Labeling: Incorrect or Missing Lot and/or Exp Date
STAQ Pharma
Labeling: Incorrect
HIGH
Health & Personal Care
HIGH
FDA DRUG
ibspot Taoscare Motion Sickness Patches Recalled Over NDA/ANDA Issue (2025)
Marketed Without an Approved NDA/ANDA
ibspot
Marketed Without
Health & Personal Care
HIGH
FDA DEVICE
Glycar SA Recalls 18 SJM Pericardial Patch EnCap 5x10 cm REF C0510 in 2025 Recall
The impacted lot may not meet the required tensile strength specification.
Glycar SA
The impacted
Health & Personal Care
HIGH
FDA DEVICE
C-RAD POSITIONING AB Recalls Catalyst Device Over Treatment Risks
C-RAD POSITIONING AB
Due to
Health & Personal Care
HIGH
FDA DRUG
USV Private Olopatadine Eye Drops 0.1% Recalled in 8,952 Bottles (2025)
Failed Impurities/Degradation Specifications: The result for 'Any individual unspecified impurity' exceeds the specification limit.
USV Private
Failed Impurities/Degradation
Food & Beverages
HIGH
FDA FOOD
Rong Shing NY Recalls Aojia Dried Red Bayberry 5.6oz for Undeclared Sulfites (2025)
Product contains undeclared sulfites (7.39mg/serving) and cyclamates
Rong Shing Trading NY
Product contains
HIGH
Health & Personal Care
HIGH
FDA DEVICE
Pivotal Health Solutions Recalls 34 Quantum Q400 Heated Massage Tables for Overheating Risk (2025)
The heat function may become damaged over time due to patients pressing on the areas with heat function components. Damage to components can lead to overheating which can lead to smoldering and melting of the vinyl cushion.
Pivotal Health Solutions
The heat
Tag Statistics
Total Recalls
2,756