BD PosiFlush SF Saline Flush Syringe 0 — Class II medical device recall Z-2673-2014
Terminated recall by Becton Dickinson & Company, reported 2014-10-01, distributed nationwide. BD received some reports of open seals found on the BD Posiflush SF Flush Syringe 10 mL (Ref #306553).
| Recall number | Z-2673-2014 |
|---|---|
| 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 | 2014-07-22 |
| Classified | 2014-09-22 |
| Reported by FDA | 2014-10-01 |
| Terminated | 2015-04-21 |
| Distributed | Nationwide (US) |
| Quantity | 3,088,320 units |
| Lot numbers | 3024261, 3046276, 4128353 |
| Model numbers | 306553 |
| Expiration dates | 2015-12, 2016-01, 2017-04 |
Product
BD PosiFlush SF Saline Flush Syringe 0.9 Sodium Chloride Injection, USP 10 mL REF 306553. Intended to be used only for the flushing of indwelling vascular access devices.10 mL BD PosiFlush Normal Saline Flush Syringes are generally compatible for use with syringe pumps.
Reason for recall
BD received some reports of open seals found on the BD Posiflush SF Flush Syringe 10 mL (Ref #306553).
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-2673-2014. 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.