Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Pacemaker Recall 2025 Affects ACCOLADE, ALTRUA 2 and CRT-P Devices Worldwide
Boston Scientific
Software to
immediate action Recalls
2,756 recalls tagged with “immediate action”.
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 Pacemaker Recall Affects 3,620 Units Worldwide in 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 ACCOLADE Pacemakers Recall 16,077 Units Worldwide (L300)
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 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 1,380 Units Over Software Safety Issue
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 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 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 Over Software Issue 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 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 Safety Architecture Software Issue (41,009 Units, 2025)
Boston Scientific
Software to
Food & Beverages
HIGH
FDA FOOD
Hershey Creamery Green Mint Chip Bulk Ice Cream Recalled for Coliform Contamination (81 Units, 2025)
Product tested elevated coliform counts during routine testing
Hershey Creamery
Product tested
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
Food & Beverages
HIGH
FDA FOOD
Great American Seafood Imports Co. Frozen Raw Shrimp Recall Covers 11,081 Cases (2025)
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
Great American Seafood Imports Co.
Product manufactured
Food & Beverages
HIGH
FDA FOOD
Best Yet, Arctic Shores, and Great American Frozen Shrimp Recalled for Cs-137 Contamination (2025)
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
Best Yet
Product manufactured
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