Health & Personal Care
HIGH
FDA DEVICE
GE HealthCare Recalls 37 Maxicam Dual-Head Gamma Cameras for Cardiac Imaging (2025)
GE HealthCare
GE HealthCare
Drug Recalls Center
2,090 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
2,090
Total Drug Recalls
24
High Risk Medications
FDA
Official Source
Important Medication Safety Information
- Do not stop taking prescribed medications without consulting your healthcare provider
- Contact your pharmacist or doctor if you have a recalled medication
- Check lot numbers carefully - not all batches may be affected
- Return recalled medications to your pharmacy for proper disposal
Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.
Health & Personal Care
HIGH
FDA DEVICE
GE Medical Systems Israel Varicam Gamma Camera Recall: 15 Units Worldwide (2025)
GE Medical Systems Israel
GE HealthCare
Health & Personal Care
HIGH
FDA DEVICE
GE Healthcare Elscint Helix Dual-Head Gamma Camera Recall for Detector Fall Risk (3 Units Worldwide,
GE Healthcare Israel Functional Imaging
GE HealthCare
Health & Personal Care
HIGH
FDA DEVICE
UIH Technologies PET/CT System Recall Affects 3 Units Over Gantry Interference Risk (2025)
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
UIH Technologies
Third-party outer
Health & Personal Care
HIGH
FDA DRUG
Major Pharmaceuticals Chlorpromazine Hydrochloride 25 mg Tablets Recall 2025 for CGMP Deviations
CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake limit
Major Pharmaceuticals
CGMP Deviations:
Health & Personal Care
HIGH
FDA DRUG
Major Pharmaceuticals Chlorpromazine Hydrochloride 100 mg Recall 2025 — 866 Blister Packs Nationwide
CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake limit
Major Pharmaceuticals
CGMP Deviations:
Health & Personal Care
HIGH
FDA DEVICE
Argon Medical Devices Recalls 1,821 Option Elite IVC Filters for Dilator Resistance Risk (2025)
Due to complaints of increased resistance when advancing the dilator within the introducer sheath. This issue could potential result in procedural delays and/or risk of venous intimal injuries if excessive force is applied
Argon Medical Devices
Due to
Health & Personal Care
HIGH
FDA DEVICE
Noah Medical Galaxy System GAL-001 Recall of 47 Units for Password-Protected Manual Access (2025)
Due to Users not having access to the Instructions for Use/User Manual due to it being password protected.
Noah Medical
Due to
Health & Personal Care
HIGH
FDA DEVICE
GE Medical Systems Israel Recalls 11 Elscint Cardial Gamma Cameras in 2025
GE Medical Systems Israel
GE HealthCare
Health & Personal Care
HIGH
FDA DEVICE
GE HealthCare Recalls SMV DSXi Nuclear Medicine Gamma Camera (205 Units) for Cardiac Imaging
GE HealthCare
GE HealthCare
Health & Personal Care
HIGH
FDA DEVICE
GE Healthcare Recalls 82 Millenium Myosight Dual-Head Gamma Cameras for Cardiac Imaging (2025)
GE Healthcare
GE HealthCare
Health & Personal Care
HIGH
FDA DEVICE
Philips Cardiac Workstation 5000 860439 Recalled After Pinched Wire Causes Short, 28 Units in U.S.
Failure of Environmental Stress Testing from a pinched power module wire within the housing of the Cardiac Workstation device which resulted in a short.
Philips North America
Failure of
Health & Personal Care
HIGH
FDA DEVICE
GE HealthCare Recalls 28 Elscint SPX6 Gamma Cameras Worldwide in 2025
GE HealthCare
GE HealthCare
Health & Personal Care
HIGH
FDA DEVICE
GE HealthCare Recalls 64 Elscint Model 4XX Gamma Cameras in 2025
GE HealthCare
GE HealthCare
Health & Personal Care
HIGH
FDA DRUG
Major Pharmaceuticals Chlorpromazine 25 mg Tablets Recalled for Nitrosamine Contamination (1256 Bls,
CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake limit
Chlorpromazine Hydrochloride
CGMP Deviations:
Health & Personal Care
HIGH
FDA DRUG
Cetirizine Hydrochloride Tablets Recall 2025 Over Wrong ID Imprint, 13,440 Bottles Nationwide
Tablet/Capsules Imprinted with Wrong ID
Cetirizine Hydrochloride
Tablet/Capsules Imprinted
Health & Personal Care
HIGH
FDA DRUG
Unique Pharmaceuticals Cetirizine Hydrochloride 10 mg Tablets Recalled Nationwide in 2025
Tablet/Capsules Imprinted with Wrong ID
Cetirizine Hydrochloride
Tablet/Capsules Imprinted
Health & Personal Care
HIGH
FDA DEVICE
GE Medical Systems Israel Recalls Elscint SPX4 Gamma Camera for Cardiac Imaging
GE Medical Systems Israel
GE HealthCare
Health & Personal Care
HIGH
FDA DEVICE
GE HealthCare Millennium MPS Dual-Head Gamma Camera Recalled for Potential Detector Fall (54 Units)
GE Medical Systems Israel, Functional Imaging
GE HealthCare
Health & Personal Care
HIGH
FDA DEVICE
GE HealthCare Optima NX Recall for Detector Fall Risk (1 Unit)
GE Medical Systems Israel Functional Imaging
GE HealthCare
Health & Personal Care
HIGH
FDA DEVICE
GE HealthCare Millenium MPR Gamma Camera Recalled for 292 Units Worldwide in 2025
GE HealthCare
GE HealthCare
Health & Personal Care
HIGH
FDA DEVICE
UIH Technologies uCT 780 MD CT Scanner Recalled for Cover Interference (2025)
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
UIH Technologies
Third-party outer
Health & Personal Care
HIGH
FDA DEVICE
UIH Technologies Recalls 11 uCT 760 MD CT Scanners for Cover Interference Risk (2025)
Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.
UIH Technologies
Third-party outer
Health & Personal Care
HIGH
FDA DEVICE
GE HealthCare Recalls 102 Dual-Head Gamma Cameras for Cardiac Imaging (2025)
GE HealthCare
GE HealthCare
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