Z-2064-2018 Class II Terminated
FDA device recall Z-2064-2018 was initiated by C.R. Bard, Inc. on December 13, 2017 and is designated Class II. Reason for recall: Foley Catheter with Incorrect Retainer Cap Print The recall status is terminated (terminated December 14, 2020). Affected quantity: N/A.
Recall Details
- Product Type
- Devices
- Report Date
- June 13, 2018
- Initiation Date
- December 13, 2017
- Termination Date
- December 14, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- N/A
Product Description
Bardex Lubricath 3-Way 75cc Continuous Irrigation Foley Catheter (Creevy), 22Fr. Rx (01267522)
Reason for Recall
Foley Catheter with Incorrect Retainer Cap Print
Distribution Pattern
FL, NY, MN and TX Canada, Japan and Taiwan
Code Information
Catalog # 01267522 Lot #'s: NGBR0383 and NGBR2129