Health & Personal Care Recalls

Zydus Lifesciences Chlorpromazine Hydrochloride Tablets 25 mg 100-count Recall 2025

CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit

Philips Philips Medical Systems Netherlands B.V. Allura Xper FD20/20 OR Table Recall Affects 3 Units

Philips Allura Xper FD20/20 Recall Affects 75 Systems Worldwide for Internal Component Deterioration

Philips Medical Systems Nederland B.V. Recalled 98 Imaging Systems for CMOS Battery, HDD, PSU Deteri

Zydus Lifesciences Chlorpromazine Hydrochloride Tablets Recalled for N-nitroso Contamination

CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit

Philips Medical Systems Nederland B.V. Allura CV20 Recalled in Global Distribution for Component D-7

Zydus Chlorpromazine Hydrochloride 10 mg Tablets Recalled for Nitrosamine Impurity (2025)

CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit

Philips Allura Xper FD20 Biplane Recall Affects 268 Units Worldwide (2025)

Zydus Lifesciences Chlorpromazine Hydrochloride 100 mg Recall 2025

CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit

Zydus Lifesciences Chlorpromazine Hydrochloride 25 mg 100-count Tablets Recalled Nationwide (2025)

CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit

Philips Allura Xper FD20/10 Recall 45 Units Worldwide in 2025

Philips Allura Xper FD20 Biplane OR Table Recall Affects 5 Units Worldwide (2025)

Philips Allura Xper FD20 OR Table Recalled for 174 Units Worldwide in 2025

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.

Viorele Desogestrel/Ethinyl Estradiol Recall 2025 for Impurities

Philips Allura Xper FD10 OR Table 722033 Recall 2 Units Worldwide (2025)

Philips Allura Xper FD20/20 Recall 115 Units Over Startup-Battery Risk (2025)

Philips Medical Systems Nederland Blames BIOS Battery Design Flaw in Allura Centron 722400 Recall (Z

Philips Medical Systems Recalls 87 BIOS Battery Models After Start-up Failure Risk

Philips Medical Systems Nederland Recall Expands for Allura Xper FD20/15 OR Table Model 722059 (2025