Health & Personal Care
HIGH
FDA DEVICE
GE HealthCare Recalls 1,386 Millennium MG/MC Gamma Cameras for Detector Mounting Risk (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 DRUG
Major Pharmaceuticals Chlorpromazine Hydrochloride 50 mg Tablets Recalled for Nitrosamine Impurity (
CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake limit
Major Pharmaceuticals
CGMP Deviations:
Health & Personal Care
HIGH
FDA DEVICE
Diagnostica Stago STA Liatest D-Di Recall 12,740 Units Worldwide in 2025
A potential risk of underestimation of D-Dimer (D-Di) levels with the two listed lots.
Diagnostica Stago
A potential
Health & Personal Care
HIGH
FDA DRUG
Major Pharmaceuticals Chlorpromazine Hydrochloride 200 mg Recall Involves 1,394 Blister Packs (2025)
CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the recommended intake limit
Chlorpromazine Hydrochloride
CGMP Deviations:
HIGH
CPSC
Blueroot Health Recalls Bariatric Fusion Iron Multivitamins Over Child Poisoning Risk (2025)
Blueroot Health
The recalled
Health & Personal Care
HIGH
FDA DEVICE
Olympus EVIS EXERA II BF-P180 Bronchovideoscope Recalled; 3,250 Units Affected Worldwide (2025)
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
Olympus Corporation of the Americas
Additional IFU
Health & Personal Care
HIGH
FDA DEVICE
Olympus BF-P150 Bronchoscope Recall Expanded Over IFU Clarifications (2025)
Olympus Corporation of the Americas recalls its BF-P150 bronchoscope after updates to the instruction for use. The recall covers 1,019 units outside the U.S. Distribution was nationwide in the U.S. The agency classifies this as a high-hazard issue.
Olympus Corporation of the Americas
Additional IFU
Health & Personal Care
HIGH
FDA DEVICE
Olympus BF-XT190 Bronchovideoscope Recall for IFU Updates Over Laser and HF Therapy Use
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
Olympus Corporation of the Americas
Additional IFU
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Recall: Preconnect with TENACIO Pump with InhibiZone Affects 172 Units Worldwide
The potential for devices to experience inflation and/or deflation performance issues or difficulties.
Boston Scientific
The potential
Health & Personal Care
HIGH
FDA DEVICE
Olympus BF-PE2 Bronchoscope Recall Expands with 4,289 Units Aboard Outside US
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
Olympus Corporation of the Americas
Additional IFU
Health & Personal Care
HIGH
FDA DEVICE
Olympus BF-1TH1100 Bronchoscope Recall Expanded for IFU Clarifications (2025)—High Risk
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
Olympus Corporation of the Americas
Additional IFU
Health & Personal Care
HIGH
FDA DEVICE
Olympus BF-Q180-AC Bronchoscope Recall Due to Safety Issues - Stop Using Now
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
Olympus Corporation of the Americas
Additional IFU
Health & Personal Care
HIGH
FDA DEVICE
Olympus BF-H190 Bronchovideoscope Recall Expanded for IFU Updates in 2025
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
Olympus Corporation of the Americas
Additional IFU
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific CX Preconnect with TENACIO Pump Recall for Inflation Issues (2025)
The potential for devices to experience inflation and/or deflation performance issues or difficulties.
Boston Scientific
The potential
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific LGX Preconnect with TENACIO Pump Recalled for Inflation/Deflation Issues (2025)
The potential for devices to experience inflation and/or deflation performance issues or difficulties.
Boston Scientific
The potential
Health & Personal Care
HIGH
FDA DEVICE
CareFusion 303 BD Alaris Infusion Sets Recalled for Flow, Bolus Accuracy Issues (2025)
Infusion pump module used with compatible pump infusion sets may perform outside the established performance ranges for flow rate and bolus accuracy, downstream and upstream occlusion time to alarm, and post-occlusion bolos volume.
CareFusion
Infusion pump
Health & Personal Care
HIGH
FDA DEVICE
Medline Excelsior Medical 0.9% Saline Flush Syringes Recalled Over Concentration Deviation (8.27M)
Medline has identified a limited quantity of saline IV flush syringes that may not meet the required concentration of sodium chloride.
Medline Industries, LP
Medline has
Health & Personal Care
HIGH
Health & Personal Care
HIGH
FDA DEVICE
Olympus BF-XT160 Bronchoscope Recall Due to High Hazard Risk — 262 Units Affected
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
Olympus Corporation of the Americas
Additional IFU
Health & Personal Care
HIGH
FDA DEVICE
Olympus BF-P60 Bronchoscope Recall Affects 6,450 Units in 2025 for IFU Updates
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
Olympus Corporation of the Americas
Additional IFU
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific TENACIO Pump Recall 2025 for Inflation Deflation Issues
The potential for devices to experience inflation and/or deflation performance issues or difficulties.
Boston Scientific
The potential
Health & Personal Care
HIGH
FDA DEVICE
Olympus EVIS EXERA III BF-Q190 Bronchovideoscope Recall Expands in 2025 for IFU Updates
Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.
Olympus Corporation of the Americas
Additional IFU
Health & Personal Care
HIGH
FDA DEVICE
Ferno Power X2 Powered Ambulance Cot Recalled for 138 Units Nationwide in 2025
Ferno-Washington Inc. recalled 138 Power X2 powered ambulance cots nationwide. The recall is due to fastening post hardware that could loosen and detach. Stop using the device and contact Ferno-Washington for instructions.
Ferno-Washington
The fastening
Health & Personal Care
HIGH
FDA DEVICE
Theken Companies Recalls 409 iNSitu Bipolar Hip System Heads for Sterile Barrier Risk (2025)
Downstream recall for RES 97605, BioPro femoral components. Product failed transit testing. Impacted product may have potential issues with sterile barrier.
Theken Companies
Downstream recall
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