Every recall we track for Oscor Inc. — 6 in all — plus the complaints and injury reports the public filed about them.
Oscor recalls Abiomed Introducer Kit (REF: 0052-3006) due to potential leakage from 14Fr and 23Fr sheaths. Affected units include specific lots with GTINs 00885672009755 and 00813502011609.
Oscor recalls Abiomed Introducer Kits (14F/23F) due to potential sheath leaks. This could cause bleeding or infection during heart pump procedures. Affected units have specific GTINs and expiry dates.
Oscor recalls Abiomed 14F Introducer Kits with potential leaks in sheaths. Affected kits have specific lot numbers and may require replacement.
Oscor recalls Destino Twist 14F (Guidestar 14F) models with possible hub separation risk. Affected units include specific model numbers and lots. No remedy stated in recall.
Oscor recalls AngioDynamics SafeSheath ULTRALITE 10:10F model VI10 due to potential open seal on sterile product. This could compromise sterility during medical procedures.
Oscor recalls TB Series Bipolar Pacing Leads with 2mm unshrouded connectors for potential connector cap sliding, risking wire breakage during movement.
