BD Nexiva Dual Port 20GA 1 — Class II medical device recall Z-1710-2019
Terminated recall by Becton Dickinson & Company, reported 2019-06-12. Leak from the septum assembly or the canister may burst under high pressure which could result in blood exposu
| Recall number | Z-1710-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Becton Dickinson & Company, Franklin Lakes, NJ, United States |
| Recall initiated | 2019-03-01 |
| Classified | 2019-06-03 |
| Reported by FDA | 2019-06-12 |
| Terminated | 2020-05-21 |
| Quantity | 6,720 units |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 00382903835362 |
| Lot numbers | 8337721 |
| Model numbers | 383536 |
| Expiration dates | 2021-11-30 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1710-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.