FDA Device recall Z-1710-2019
BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system Catalog Number: 383536
- FDA Device
- Class II
- terminated
- Published 2019-06-12
On 2019-06-12 the FDA classified a Class II recall of BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system Catalog Number: 383536 by Becton Dickinson And, citing leak from the septum assembly or the canister may burst under high pressure which could result in blood exposure to a health care worker.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1710-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-03-01 |
| Published | 2019-06-12 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Becton Dickinson And |
| Distribution | VA |
Product
BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system Catalog Number: 383536
Reason
Leak from the septum assembly or the canister may burst under high pressure which could result in blood exposure to a health care worker.
Identifiers
| code_info | Lot Number: 8337721 Exp. 30-Nov-2021 UDI: 382903835362 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1710-2019%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.