Oscor, Inc. recalls
7 recalls in our records from 2012 to 2026: 7 FDA medical devices.
Recalls with full detail pages
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Oscor Inc. medical device recall: Abiomed REF: 0052-3025
Due to manufacturing issues, there is a potential for the 14Fr and 23Fr introducer sheaths to leak from the sidearm, under the sheath cap, and along the hub score lines…
Earlier and other recalls
These link to the official agency notice.
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Oscor Inc. medical device recall: Destino Twist 14F Official notice ↗
There is potential for separation between the threaded hub and threaded cap at the proximal end of the device.
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Oscor, Inc. medical device recall: AngioDynamics SafeSheath ULTRALITE 10F Official notice ↗
Potential for open seal on sterile product
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Oscor, Inc. medical device recall: TB Series Bipolar Pacing Leads Official notice ↗
During the use of some TB - Temporary Bipolar Pacing Leads, featuring the 2mm unshrouded connectors, the connector cap housing may slide and potentially expose the…
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Oscor, Inc. medical device recall: ATAR Reusable Extension Cable Official notice ↗
The Reusable Oscor ATAR extension cables could separate from the connector during use.
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Oscor, Inc. medical device recall: OSCOR ADELANTE BREEZEWAY 8F C55¿ S61CM D66CM Catalog # AB081040 Is… Official notice ↗
Complaint that during insertion of the dilator through the sheath a fragment of inner liner came out of the sheath prior to use.
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Oscor, Inc. medical device recall: Myocardial Heart Wires Intended for temporary atrial and ventricular… Official notice ↗
Oscor, Inc. in Palm Harbor, FL is recalling myocardial heart wires, models TME60S, TME64S, TME64C, TME64S-3, TME65S, and TME66S. The recall was initiated due to the…
Firm names are matched across agencies by name only. Different companies with similar names may be grouped together; check each official notice.