Oscor recalls

2 official recalls and safety alerts involving Oscor since 2022-02, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.

This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Oscor or the relevant agency.

1. 2026-07-22
2. US
   Drugs & medicalClass I

   Oscor Inc. recalls Abiomed REF: 0052-3025, Introducer Kit for Impella Hemostatic Peel Away Introducer System with Infusion Sideport, 14F 13cm and 25cm. heart…

   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 in the hub region.

   FDA · DeviceOscor Inc.Distribution in the US state of MAOfficial notice →
3. 2022-02-23
4. US
   Drugs & medicalClass II

   Oscor Inc. recalls Destino Twist 14F (also branded as Guidestar 14F)

   There is potential for separation between the threaded hub and threaded cap at the proximal end of the device.

   FDA · DeviceOscor Inc.Distribution to TN and PA in USA OUS distribution to Czech RepublicOfficial notice →