Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland B.V. Allura CV20 Recalled in Global Distribution for Component D-7
Philips Medical Systems Nederland B.V.
Systems may
stop use immediately Recalls
2,229 recalls tagged with “stop use immediately”.
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland B.V. Recalled 98 Imaging Systems for CMOS Battery, HDD, PSU Deteri
Philips Medical Systems Nederland B.V.
Systems may
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20/20 Recall Affects 75 Systems Worldwide for Internal Component Deterioration
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Systems may
Health & Personal Care
HIGH
FDA DRUG
Zydus Lifesciences Chlorpromazine Tablets Recalled for N-Nitroso Desmethyl Chlorpromazine Beyond FDA
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
Zydus Lifesciences
CGMP Deviations:
Health & Personal Care
HIGH
FDA DRUG
Zydus Lifesciences Chlorpromazine Hydrochloride Tablets Recalled for N-nitroso Contamination
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
Zydus Lifesciences
CGMP Deviations:
Health & Personal Care
HIGH
FDA DRUG
Sun Pharmaceutical Radiopharmaceutical Kit Recall: 1,870 Kits Recalled for OOS Dissolution Issue
Failed Dissolution Specifications-Out of Specification (OOS) observation for sulphate in Sodium Tartrate Dihydrate used for the production of Mertiatide.
Sun Pharmaceutical Industries
Failed Dissolution
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
Inpeco Recall: 8 FlexLab FLX Potassium Test System Units Over Unverified HIL Function (2025)
Inpeco
The FlexLab
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
Philips Medical Systems Recalls 87 BIOS Battery Models After Start-up Failure Risk
Philips Medical Systems Nederland B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Recalling 298 Allura Xper FD20 OR Tables Worldwide Over BIOS Battery Risk (2025)
Philips
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
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 Medical Systems FD20 Biplane OR Table Recall for BIOS Battery Depletion (2025)
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
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
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
Food & Beverages
HIGH
FDA FOOD
New Spirit Naturals Ultra Whey Protein Powder Recalled for Undeclared Milk Allergen
New Spirit Naturals
undeclared allergen
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 FD10/10 Recall Tied to BIOS Battery Depletion
Philips Medical Systems Nederland B.V.
The BIOS