Health & Personal Care
HIGH
FDA DEVICE
PHILIPS IntelliSpace Cardiovascular Software 8.0.0.4 Recall Affects 4 Units Nationwide
Software issue that results in the display of outdated information.
Philips Medical Systems Nederland B.V.
Software issue
These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
Immediate attention
High Risk Recalls
3,585 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
- High-risk recalls
- 3,585
- Action level
- Stop use
What to do if you own a recalled product
- Stop using the product immediately
- Keep the product away from children
- Follow the remedy instructions provided
- Contact the manufacturer for a refund or replacement
Food & Beverages
HIGH
FDA FOOD
SUNGAL UDK Half Plum 170 g Recall for Cyclamate Adulteration (2025)
SUNGAL
Cyclamate adulteration
Health & Personal Care
HIGH
FDA DEVICE
Baxter Continu-Flo Intravascular Set Recalled for Tubing Separation — 14,400 Units in 2025
Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for one lot of Continu-Flo solution sets listed below due to customer reports of tubing separation.
Baxter Healthcare
Baxter Healthcare
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 DRUG
Quallent Pharmaceuticals Health LLC Recall Expands for Duloxetine Delayed-Release Capsules Over Imp-
CGMP deviations: N-nitroso-duloxetine impurity above the proposed interim limit.
DULOXETINE
CGMP deviations:
Health & Personal Care
HIGH
FDA DEVICE
Medline Medline Extremity Pack DYNJ45701B Sterile Kit Recall Affects 88 Units (2025)
Convenience kits labeled as sterile have not gone through the sterilization process.
Medline Industries
Convenience kits
Health & Personal Care
HIGH
FDA DEVICE
Medline Industries Recalls 22 Sterile Convenience Kits DYNJ0382730O, DYNJ61038B (2025)
Convenience kits labeled as sterile have not gone through the sterilization process.
Medline Industries
Convenience kits
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
CPSC
AliExpress Recalls LeymanKids Children's Pajama Sets for Burn Risk in 2025 Recall
AliExpress
The recalled
HIGH
CPSC
Monica Vinader Recalls 14k Yellow Gold Mini Heart Jewelry Over Cadmium Levels (2025)
Monica Vinader
The jewelry
HIGH
CPSC
Fieldsheer Recalls Heated Socks MWMS07 MWWS07 MWMS05 for Burn Hazard (2025)
Fieldsheer Apparel Technologies
The socks
CRITICAL
CPSC
Séfralls Minoxidil Hair Generation Serum Recalled for Child Poisoning Risk (2025)
This recall involves Séfralls Hair Generation Serum. The hair serum comes in an amber dropper bottle with a white and gold dropper and a white, black and gold label. "Séfralls" and "Minoxidil" are printed on the label located on the front of the bottle.
Séfralls
The hair
Food & Beverages
HIGH
FDA FOOD
Wang Globalnet Recalled 1,705 Frozen Oyster Halves Over Norovirus Risk (2025)
Oyster product potentially contaminated with Norovirus
Wang Globalnet
Oyster product
Health & Personal Care
HIGH
FDA DRUG
Glenmark Carvedilol Tablets Recalled Over Nitrosamine Impurity
CGMP Deviations: Presence of a nitrosamine, N-Nitroso Carvedilol I Impurity above the current Acceptable Intake Level.
Glenmark Pharmaceuticals Inc.
CGMP Deviations:
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:
Health & Personal Care
HIGH
FDA DRUG
Glenmark Carvedilol 3.125 mg Recall for Nitrosamine Impurity Affects 44,328 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
TEMI Go Basketball Toy Recalled for Choking Hazard Sold on Amazon (2025)
TEMI Go Basketball Toys
The recalled
HIGH
CPSC
Petmate Pet Zone Laser Pointer & LED Ball Toys Recalled for Button Battery Ingestion Risk Sold atMen
Petmate
The recalled
HIGH
HIGH
CPSC
Deale International Recalls Altafit AF28 Smartwatches Sold by HSN for Fire Hazard
Deale International
The smartwatch's