BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547 — Class II medical device recall Z-0499-2020
Terminated recall by Becton Dickinson & Company, reported 2019-11-27, distributed nationwide. Limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with stand
| Recall number | Z-0499-2020 |
|---|---|
| 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 | 2019-10-14 |
| Classified | 2019-11-20 |
| Reported by FDA | 2019-11-27 |
| Terminated | 2020-10-16 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 1,632,000 |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 50382903065474 |
| Lot numbers | 9142881 |
| Model numbers | 306547 |
Product
BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306547
Reason for recall
Limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with standard BD Posiflush Pre-Filled Normal Saline Syringes.
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-0499-2020. 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.