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
These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
Immediate attention
High Risk Recalls
4,262 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
- High-risk recalls
- 4,262
- Action level
- Stop use
What to do if you own a recalled product
- Stop using the product immediately
- Keep the product away from children
- Follow the remedy instructions provided
- Contact the manufacturer for a refund or replacement
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 Recall 28,911 U128 ACCOLADE, VISIONIST VALITUDE CRT-P Devices (2025)
Boston Scientific
Software to
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Pacemaker L231 Recalled; 63,851 Units in 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 ACCOLADE Pacemakers Recall 16,077 Units Worldwide (L300)
Boston Scientific
Software to
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Pacemaker Recall Affects 3,620 Units Worldwide in 2025
Boston Scientific
Software to
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Pacemakers Recall 1,380 Units Over Software Safety Issue
Boston Scientific
Software to
Food & Beverages
HIGH
FDA FOOD
Toto Foods Gluten Free Cookie Recalled for Soy Label Conflicts, 120,180 Units Affected (2025)
Product label contains conflicting statements about inclusion and being free of Soy ingredient.
Toto Foods
Product label
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 Safety Architecture Software Issue (41,009 Units, 2025)
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 Recall 10,833 Units in 2025 Over Software Hazard
Boston Scientific
Software to
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 Recalled Over Software Flaw in Safety Architecture (2025)
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 DEVICE
Boston Scientific Pacemakers Recalled Over Software Issue in Safety Architecture (2025)
Boston Scientific
Software to
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Pacemakers Recalled in Class I High-Hazard Software Issue Affecting ACCOLADE, VERS
Boston Scientific
Software to
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific ESSENTIO DR EL MRI Pacemaker Recalled for Software Safety Issue (190,088 Units, 0)
Boston Scientific
Software to
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