BD Nexiva Closed IV Catheter System Dual Port — Class II medical device recall Z-0125-2021
Terminated recall by Becton Dickinson & Company, reported 2020-10-28, distributed nationwide. Dull/blunt needles within the IV Catheter System may lead to missed insertion attempts and delay in diagnosis
| Recall number | Z-0125-2021 |
|---|---|
| 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 | 2020-09-14 |
| Classified | 2020-10-19 |
| Reported by FDA | 2020-10-28 |
| Terminated | 2021-09-27 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, MX |
| Quantity | 12,020 units |
| UPC / GTIN / UDI-DI | 30382903835387 |
| Lot numbers | 9325212 |
| Model numbers | 383538BD |
Product
BD Nexiva Closed IV Catheter System Dual Port (20 GA 1.75 IN) Catalog (Ref) No. 383538 BD Nexiva closed IV catheter systems are intended to be inserted into a patient s vascular system for short term use to sample blood, monitor blood pressure, or administer fluids.
Reason for recall
Dull/blunt needles within the IV Catheter System may lead to missed insertion attempts and delay in diagnosis or treatment until a new needle is inserted
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-0125-2021. 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.