Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Pacemakers Recalled Over Software Flaw in Safety Architecture (2025)
Boston Scientific
Software to
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
Boston Scientific Pacemaker Recall 2025 Affects 41,191 ACCOLADE, Visionist and Valitude Devices
Boston Scientific
Software to
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Pacemakers Recall 10,833 Units in 2025 Over Software Hazard
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 Pacemakers Recalled for Safety Architecture Software Issue (41,009 Units, 2025)
Boston Scientific
Software to
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Pacemakers Recalled for High Battery Impedance Safety Software
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 L221 PROPONENT DR EL Pacemaker Recalled for Safety Software Issue (2025)
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 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 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 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 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
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 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
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 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
Related Categories
Category Statistics
Total Recalls
1,882
Pages
95