Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland Blames BIOS Battery Design Flaw in Allura Centron 722400 Recall (Z
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
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
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland Recall Expands for Allura Xper FD20/15 OR Table Model 722059 (2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20 BiOS Battery Recall Affects 5,067 Units Worldwide
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Inpeco FlexLab X System Potassium Test System Recalled for Unvalidated Hemolysis, Icterus, Lipemia H
Inpeco S.A.
The FlexLab
Health & Personal Care
HIGH
FDA DRUG
Viorele Desogestrel/Ethinyl Estradiol Recall 2025 for Impurities
Viorele
Failed Impurities/Degradation
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems FD20 Biplane OR Table Recall for BIOS Battery Depletion (2025)
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
Food & Beverages
HIGH
FDA FOOD
New Spirit Naturals Ultra Whey Protein Powder Recalled for Undeclared Milk Allergen
New Spirit Naturals
undeclared allergen
Food & Beverages
HIGH
FDA FOOD
New Spirit Naturals Gluta Plus Glutathione 60-Capsule Recall for Milk Allergy Hazard
New Spirit Naturals
undeclared allergen
Food & Beverages
HIGH
FDA FOOD
New Spirit Naturals Protein Powder Recall Affects 79 Units Over Milk Allergen Disclosure
New Spirit Naturals
undeclared allergen
Food & Beverages
HIGH
FDA FOOD
New Spirit Naturals Recalled 178 Units of Super Muscle Support Powder for Milk Allergen (2025)
New Spirit Naturals
undeclared allergen
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20/20 Recall 115 Units Over Startup-Battery Risk (2025)
Philips Medical Systems Nederland
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD10C Recall for 2 US Units Over BIOS Battery Startup Failure (2025)
Philips Medical Systems Nederland B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland recalls 5 Allura Xper FD20/20 OR Tables for BIOS battery startup
Philips Medical Systems Nederland B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20 Biplane Recalled for BIOS Battery Failure in 501 Units (2025)
Philips Medical Systems Nederland
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Beckman Coulter Phosphorus Reagent Recall: 2,146 Units for Calibration Failures
Specific SYNCHRON Systems Modular Chemistry Phosphorus (PHOSm REF 467868) reagent lots may fail calibration before the lot expiration date which causes a delay in obtaining patient results.
Beckman Coulter
Specific SYNCHRON
Health & Personal Care
HIGH
FDA DEVICE
PHILIPS Allura Xper FD10/10 Recall Tied to BIOS Battery Depletion
Philips Medical Systems Nederland B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland Recall: BIOS Battery Causes Startup Failures in Allura Xper CV20 7
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
Health & Personal Care
HIGH
FDA DRUG
High-Risk Antibiotic Recall: Sulfamethoxazole and Trimethoprim 800/160 mg Double Strength Packets Re
Presence of a Foreign Substance: A specific lot of auxiliary polyester coil, used in product packaging by manufacturer (Amneal Pharmaceuticals LLC) was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
SULFAMETHOXAZOLE AND TRIMETHOPRIM
Presence of
Health & Personal Care
HIGH
FDA DRUG
Major Pharmaceuticals Sulfamethoxazole and Trimethoprim 800 mg/160 mg 100-Tablets Recall 2025
Presence of a Foreign Substance: A specific lot of auxiliary polyester coil, used in product packaging by manufacturer (Amneal Pharmaceuticals LLC) was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Sulfamethoxazole and Trimethoprim
Presence of
Health & Personal Care
HIGH
FDA DRUG
AvKARE Norgestimate and Ethinyl Estradiol Tablets Recall for Uniformity Issue (2025)
AvKARE
Failed Content