Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems Recalls 32,433 Medical Convenience Kits Over EO Re-Gassing Risk (2025)
American Contract Systems
Identified products
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 DEVICE
American Contract Systems Labor Delivery Packs Recalled for Re-Gassed Sterilization Flaw (2025)
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems Medical Convenience Kits Recalled for Re-Gassing Risk
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems LKRA40G Radiology Pack Recalled Over Unvalidated Re-sterilization (HIGH)
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems IHDC30R D AND C PACK Medical Kits Recalled Over Re-Gassing (32,433 Units,
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems Recalled 32,433 Orthopedic Surgical Kits Over Re-Gassing Risk (2025)
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems Recalls 32,433 Medical Convenience Kits Over Re-Gassing Risk (2025)
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
Lutronic XERF EFFECTOR 60 Electrosurgical Unit Recalled for Manufacturing Defects (2025-2026 Models)
Manufacturing defects in devices manufactured from 4/1/25 to 8/20/25 can on rare occasions result in adverse events for patients.
Lutronic
Manufacturing defects
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems Recalls 32,433 Angio Packs Over Re-Gassed EO Sterilization (2025)
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems High-Rire Recall: 32,433 Medical Convenience Kits Recalled for Re-GassedEO
American Contract Systems
Identified products
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20 Recall Affects 2,114 Units Globally Over Power Component Deterioration
Philips Medical Systems
Systems may
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD10 Recall 2025: 1,117 Imaging Systems Worldwide Face Movement-Dysfunction Risk
Philips
Systems may
Health & Personal Care
HIGH
FDA DRUG
Zydus Chlorpromazine Hydrochloride 200 mg Recall Expands Nationwide Over CGMP Deviations
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
Chlorpromazine Hydrochloride
CGMP Deviations:
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD10 OR Table Recall for 2 Units Worldwide in 2025
Philips Medical Systems Nederland B.V.
Systems may
Health & Personal Care
HIGH
FDA DRUG
Zydus Lifesciences Chlorpromazine Hydrochloride 100 mg Recall 2025
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 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 Recall 100-Count Bottles (2025)
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
Zydus Lifesciences
CGMP Deviations:
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD10/10 Recall for 286 Units Worldwide in 2025
Philips Medical Systems Nederland B.V.
Systems may
Health & Personal Care
HIGH
FDA DRUG
Zydus Lifesciences Chlorpromazine Hydrochloride Tablets 50 mg 100-count Recall 2025
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
Zydus Lifesciences
CGMP Deviations:
Health & Personal Care
HIGH
FDA DEVICE
Philips Recalls 1 Allura Xper FD20/15 OR Table for Movement Failure Risk (2025)
Philips
Systems may
Related Categories
Category Statistics
Total Recalls
1,882
Pages
95