Z-1710-2019 Class II Terminated
FDA device recall Z-1710-2019 was initiated by Becton Dickinson & Company on March 1, 2019 and is designated Class II. Reason for recall: Leak from the septum assembly or the canister may burst under high pressure which could result in blood exposure to a health care worker. The recall status is terminated (terminated May 21, 2020). Affected quantity: 6,720 units.
Recall Details
- Product Type
- Devices
- Report Date
- June 12, 2019
- Initiation Date
- March 1, 2019
- Termination Date
- May 21, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 6,720 units
Product Description
BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system Catalog Number: 383536
Reason for Recall
Leak from the septum assembly or the canister may burst under high pressure which could result in blood exposure to a health care worker.
Distribution Pattern
US distribution to one distributor in VA.
Code Information
Lot Number: 8337721 Exp. 30-Nov-2021 UDI: 382903835362