Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Pacemakers Recalled for Safety Architecture Software Issue (41,009 Units, 2025)
Boston Scientific
Software to
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
Boston Scientific Pacemakers Recalled for Safety-Mode Initiation Software Flaw (2025)
Boston Scientific
Software to
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific L211 PROPONENT DR SL MRI Pacemakers Recalled Worldwide (106,536 Units, 2025)
Boston Scientific
Software to
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Pacemakers Recalled for Software Safety Issue Affecting 12,326 Units (2025)
Boston Scientific
Software to
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Recalls 22,714 ACCOLADE Pacemakers Over Software Safety Issue (2025)
Boston Scientific
Software to
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Pacemaker Recall 2025 Affects ACCOLADE, ALTRUA 2 and CRT-P Devices Worldwide
Boston Scientific
Software to
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Pacemakers Recalled in 2025 for Safety Architecture Software Flaw
Boston Scientific
Software to
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific L110 ESSENTIO SR SL MRI Pacemaker Recalled in 2025 for 61,700 Units
Boston Scientific
Software to
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Pacemakers Recalled for Software Flaw That Could Block Safety Mode
Boston Scientific
Software to
Health & Personal Care
HIGH
FDA DRUG
Lannett 10mg Dextroamphetamine Tablets Recalled for Foreign Tablet Contamination (2025)
Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate
Presence of
Health & Personal Care
HIGH
FDA DRUG
READYPREP PVP Iodine 10% Topical Antiseptic Recalled for Subpotent Drug (Medline)
FDA recalls READYPREP PVP, povodone-iodine 10% topical antiseptic. Medline Industries issued the nationwide recall. Subpotent drug is the reason. Consumers should stop using the product immediately.
POVIDONE-IODINE
Subpotent drug
Health & Personal Care
HIGH
FDA DRUG
Chlorpromazine Hydrochloride 200 mg Recall Expanded After Packaging Contamination Found in 3,363 JDS
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Chlorpromazine Hydrochloride
Presence of
Health & Personal Care
HIGH
FDA DRUG
Amneal Chlorpromazine Hydrochloride 50 mg Tablets Recall 2025 (13,130 Bottles)
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Chlorpromazine Hydrochloride
Presence of
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific ICEfx Cryoablation System Recalled for 19 Units Worldwide (2025)
Certain desiccant tube subassemblies were built with end caps that were not correctly tightened.
Boston Scientific
Certain desiccant
Health & Personal Care
HIGH
FDA DEVICE
Preventive Maintenance (PM) Kit ICEFX, Material Number (UPN) SPRPM8000
Certain desiccant tube subassemblies were built with end caps that were not correctly tightened.
Boston Scientific
Certain desiccant
Health & Personal Care
HIGH
FDA DRUG
B. Braun Lactated Ringers Injection 46,032 Containers Recalled Over Particulate Matter
B Braun Medical
Presence of
Health & Personal Care
HIGH
FDA DRUG
Amneal Chlorpromazine Hydrochloride Recall 2025: 14,923 Bottles Over Packaging Contamination
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Chlorpromazine Hydrochloride
Presence of
Health & Personal Care
HIGH
FDA DRUG
Amneal Chlorpromazine Hydrochloride 25 mg 100-count Recalled in 2025 for Packaging Contamination
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
Chlorpromazine Hydrochloride
Presence of
Health & Personal Care
HIGH
FDA DRUG
Amneal 800mg/160mg Sulfamethoxazole and Trimethoprim Tablets Recalled for Foreign Packaging Material
Presence of a foreign substance.A specific lot of auxiliary polyester coil, used in product packaging was detected with presence of a micro-organism. No micro-organism was detected on any tablets.
SULFAMETHOXAZOLE AND TRIMETHOPRIM
Presence of
Health & Personal Care
HIGH
FDA DRUG
B. Braun Sodium Chloride Injection 1000 mL Recalled nationwide for particulates (Class I)
B. Braun Medical Inc. recalls 47,148 containers of 0.9% Sodium Chloride Injection USP nationwide after detecting particulate matter. The Class I recall affects bottles with NDC 0264-7800-09. Stop using and contact providers for guidance.
B. Braun Medical Inc.
Presence of
Health & Personal Care
HIGH
FDA DEVICE
Aesculap AG Recalls ELAN 4 Fixed Duraguard Long Mislabeling Devices (GB943R)
Mislabeling. The ELAN 4 FIXED DURAGUARD STANDARD was labeled as "Long" and the ELAN 4 FIXED DURAGUARD LONG was labeled as "Standard."
Aesculap AG
Mislabeling. The
Health & Personal Care
HIGH
FDA DEVICE
CorNeat Vision EverPatch Recalled for Conjunctival Wound Dehiscence Risk (630 Units, 2025)
Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.
CorNeat Vision
Reviewed complaints
Health & Personal Care
HIGH
FDA DEVICE
Aesculap ELAN 4 Fixed Duraguard Recalled for Mislabeling (1 Unit, 2025)
Mislabeling. The ELAN 4 FIXED DURAGUARD STANDARD was labeled as "Long" and the ELAN 4 FIXED DURAGUARD LONG was labeled as "Standard."
Aesculap AG
Mislabeling. The
Health & Personal Care
HIGH
FDA DEVICE
Corneat Vision EverPatch+ 180-Unit Recall for Scleral Patch Dehiscence Risk (2025)
Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.
CORNEAT VISION
Reviewed complaints
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