Class IIOngoingZ-1377-2026
Olympus Corporation Of The Americas recalls Olympus Thunderbeat
Firm is initiating a removal due to continued reports of adverse events.
Olympus Corporation of…PAFeb 25, 2026
Class II recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1,093–1,104 of 3,866 recalls
Class IIOngoingZ-1376-2026
Olympus Corporation Of The Americas recalls Olympus Thunderbeat 5 mm
Firm is initiating a removal due to continued reports of adverse events.
Olympus Corporation of…PAFeb 25, 2026
Class IIOngoingZ-1375-2026
Olympus Corporation Of The Americas recalls Olympus Thunderbeat 5 mm
Firm is initiating a removal due to continued reports of adverse events.
Olympus Corporation of…PAFeb 25, 2026
Class IIOngoingZ-1374-2026
Olympus Corporation Of The Americas recalls Olympus Thunderbeat
Firm is initiating a removal due to continued reports of adverse events.
Olympus Corporation of…PAFeb 25, 2026
Class IIOngoingZ-1373-2026
Olympus Corporation Of The Americas recalls Olympus Thunderbeat 5 mm
Firm is initiating a removal due to continued reports of adverse events.
Olympus Corporation of…PAFeb 25, 2026
Class IIOngoingZ-1372-2026
Olympus Corporation Of The Americas recalls Olympus Thunderbeat
Firm is initiating a removal due to continued reports of adverse events.
Olympus Corporation of…PAFeb 25, 2026
Class IIOngoingZ-1371-2026
Olympus Corporation Of The Americas recalls Olympus Thunderbeat 5 mm
Firm is initiating a removal due to continued reports of adverse events.
Olympus Corporation of…PAFeb 25, 2026
Class IIOngoingZ-1370-2026
Medica Corporation recalls Medica Capillary Tubes
A systematic positive bias of up to 20% was identified across the reportable potassium range, resulting in false elevation results of patient samples when using Medica s capillary tubes.
Medica CorporationMAFeb 25, 2026
Class IIOngoingZ-1369-2026
Immunotech A.S. recalls Estrone RIA
The affected Estrone RIA kit lots may rarely give falsely high patient results which might cause Temporary injury of Remote probability. Only in some (very rare) cases may the issue occur.
Immunotech A.S.Feb 25, 2026
Class IIOngoingZ-1368-2026
Baxter Healthcare Corporation recalls Brand Name: Spectrum IQ Product Name: Infusion Pump Model/Catalog Number: 3570009 So…
Pumps were released without full testing being performed, including occlusion alarm testing.
Baxter Healthcare Corp…ILFeb 25, 2026
Class IIOngoingZ-1367-2026
Bard Peripheral Vascular Inc recalls Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff…
Due to damage to outer tray that can potentially compromise the sterile barrier
Bard Peripheral Vascul…AZFeb 25, 2026
Class IIOngoingZ-1366-2026
Medline Industries, LP recalls Medline Industries IV Administration and Extension Sets: 1) DBD-IV ADMIN SET
Under circumstances involving exposure to particular chemicals and mechanical forces, the male luer connectors for the specified IV Administration and Extension sets may leak, crack, and/or break during use, which may r…
Medline Industries, LPILFeb 25, 2026