Home / Recalls / Creganna Medical Devices / Z-2530-2017

Z-2530-2017 Class II Terminated

Recalled by Creganna Medical Devices — Galway, N/A

Recall Details

Product Type
Devices
Report Date
June 21, 2017
Initiation Date
May 22, 2017
Termination Date
May 29, 2018
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
150 units

Product Description

Boston Scientific Zurpaz(TM) MEDIUM CURL, SYMMETRIC CURVE, Steerable Sheath, 8.5F (2.83mm), REF Catalog No M004USMC85100

Reason for Recall

Lack of sterility assurance.

Distribution Pattern

Distributed in MA.

Code Information

Lot # 383271, 384264

Other recalls by Creganna Medical Devices

  • Z-2249-2023 Class II — Gore Tips Set Device, Catalog Number TSET1016, percutaneous liver access (June 22, 2023)
  • Z-2532-2017 Class II — Boston Scientific Zurpaz(TM) MEDIUM CURL, ASYMMETRIC CURVE, Steerable Sheath, 8. (May 22, 2017)
  • Z-2531-2017 Class II — Boston Scientific Zurpaz(TM) MEDIUM CURL, ASYMMETRIC CURVE, Steerable Sheath, 8. (May 22, 2017)
  • Z-2529-2017 Class II — Boston Scientific Zurpaz(TM) MEDIUM CURL, ASYMMETRIC CURVE, Steerable Sheath, 8. (May 22, 2017)