Health & Personal Care
HIGH
FDA DRUG
Kroger 70% Isopropyl Alcohol Recall Expands for Cross-Contamination Risk
Cross Contamination with Other Products.
Kroger
Cross Contamination
Category hub
Health & Personal Care Recalls
1,882 product recalls found in this category. Browse active safety alerts and related categories from the same official source network.
- Active recalls
- 1,882
- Pages
- 95
High activity category
This category has a significant number of recalls. Check it regularly if you own products in this area.
Health & Personal Care
HIGH
FDA DRUG
Chlorpromazine Hydrochloride 100 mg Recall Affects 2,003 Cartons Nationwide for Foreign Substance
Presence of a foreign substance.
CHLORPROMAZINE HYDROCHLORIDE
Presence of
Health & Personal Care
HIGH
FDA DRUG
AvKare Chlorpromazine Hydrochloride 50 mg Tablets Recalled for Foreign Substance Contamination (2025
Presence of a foreign substance.
AvKare
Presence of
Health & Personal Care
HIGH
FDA DRUG
TopCare Health 70% Isopropyl Alcohol Recall Expands to 60 Bottles Nationwide (2025)
Cross Contamination with Other Products.
TopCare Health
Cross Contamination
Health & Personal Care
HIGH
FDA DEVICE
LeMaitre Vascular Artegraft 10-Unit Recall 2025 for Labeling Errors
Devices were distributed with incorrect label without CE and UKCA mark, missing patient leaflet and patient implant card.
LeMaitre Vascular
Devices were
Health & Personal Care
HIGH
FDA DEVICE
CooperVision Recalls 180 Softmed Breathables Toric Lenses Over Invalid Sterilization Cycle (2025)
One lot manufactured with an invalid sterilization cycle.
CooperVision
One lot
Health & Personal Care
HIGH
FDA DRUG
Ultra Violette Velvet Screen SPF 50 Sunscreen Recalled for SPF Inconsistency; 49,275 Tubes Affected
Subpotent/Super-potent Product: Testing of the SPF 50 sunscreen revealed inconsistency in SPF results ranging from SPF 4, 10, 21, 26, 33, 60, 61, and 64.
ULTRA VIOLETTE VELVET SCREEN BLURRING MINERAL SKINSCREEN
Subpotent/Super-potent Product:
Health & Personal Care
HIGH
FDA DEVICE
CooperVision Voyant 1-Day Premium Toric Contact Lens Recalled for Invalid Sterilization Cycle
One lot manufactured with an invalid sterilization cycle.
CooperVision
One lot
Health & Personal Care
HIGH
FDA DRUG
Ultra Violette Mini Mates SPF 50 Kit Recalled for SPF Variability in 44,497 Tubes (2025)
Ultra Violette Mini Mates SPF 50 kit sold nationwide in the U.S. is recalled. Testing showed SPF results ranging from 4 to 64. The recall is issued by Grace & Fire USA Inc. The public was notified by letter.
ULTRA VIOLETTE MINI MATES
Subpotent/Super-potent Product:
Health & Personal Care
HIGH
FDA DEVICE
CooperVision MyDay Toric Contact Lenses Recalled for Invalid Sterilization Cycle
CooperVision recalled 4,140 MyDay Toric contact lenses sold nationwide in the United States. The recall cites an invalid sterilization cycle for one lot. Patients should stop wearing the lenses and consult their eye care providers for guidance.
CooperVision
One lot
Health & Personal Care
HIGH
FDA DEVICE
GE Medical Systems MAC VU360 Recall 29,225 Trunk Cable and Module Holder Units (2025)
GE Medical Systems
If a
Health & Personal Care
HIGH
FDA DEVICE
Abbott Point Of Care i-STAT EG7+ Cartridges Recalled Over 6.1 Million Units in 2025
Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+ cartridges to reflect updated sample type for potassium and ionized calcium and measurement ranges for pH and PO2.
Abbott Point Of Care
Lack of
Health & Personal Care
HIGH
FDA DEVICE
Abbott i-STAT CG8+ Cartridge Recall 2025: 8,962,450 Units
Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+ cartridges to reflect updated sample type for potassium and ionized calcium and measurement ranges for pH and PO2.
Abbott Point Of Care
Lack of
Health & Personal Care
HIGH
FDA DEVICE
Frontier Devices Recalls 2,700 REF 301.914S1 14 mm Distraction Pins (2025)
Labeling includes shelf life that has not been validated.
Frontier Devices
Labeling includes
Health & Personal Care
HIGH
FDA DEVICE
Abbott i-STAT CG8+, EG7+, EG6+ Cartridges Recalled in 2025 Over Missing 510(k) Clearance
Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+ cartridges to reflect updated sample type for potassium and ionized calcium and measurement ranges for pH and PO2.
Abbott Point Of Care
Lack of
Health & Personal Care
HIGH
FDA DEVICE
Frontier Devices Recalls 160 301.912S2 12 mm Distraction Pin Over Unvalidated Shelf-Life Labeling (Z
Labeling includes shelf life that has not been validated.
Frontier Devices
Labeling includes
Health & Personal Care
HIGH
FDA DEVICE
Frontier Devices 301.914S2 14 mm Distraction Pin Recalled for Unvalidated Shelf Life (High Risk)
Labeling includes shelf life that has not been validated.
Frontier Devices
Labeling includes
Health & Personal Care
HIGH
FDA DEVICE
Abbott i-STAT CG4+ Cartridge Recall: 9,067,050 Units Across U.S. With 510(k) Clearance Issue (2025)
Lack of a 510(k) premarket clearance for the i-STAT CG4+ cartridge to reflect updated sample type for lactate and measurement ranges for pH and PO2.
Abbott Point Of Care
Lack of
Health & Personal Care
HIGH
FDA DEVICE
Frontier Devices 301.916S1 16 mm Distraction Pin Recall Expanded (2025)
Labeling includes shelf life that has not been validated.
Frontier Devices
Labeling includes
Health & Personal Care
HIGH
FDA DEVICE
Frontier Devices 301.912S1 12 mm Distraction Pin Recall Expanded to 3,790 Units (Rx Only)
Labeling includes shelf life that has not been validated.
Frontier Devices
Labeling includes
Related Categories
Category Statistics
Total Recalls
1,882
Pages
95