BD Posiflush SF Saline Flush Syringe — Class II medical device recall Z-2065-2020
Terminated recall by Becton Dickinson & Company, reported 2020-05-27, distributed nationwide. This product has been confirmed to exhibit holes in the packaging, which impacts package integrity and potenti
| Recall number | Z-2065-2020 |
|---|---|
| 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 | 2020-04-16 |
| Classified | 2020-05-20 |
| Reported by FDA | 2020-05-27 |
| Terminated | 2021-09-01 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BE, CA, CH, DE, DK, ES, FI, FR, GB, IT, MX, MY, NL, NO, NZ, PT, SE |
| Quantity | 16,099,310 units |
| Reason classes | sterility, packaging |
| UPC / GTIN / UDI-DI | 50382903065535 |
| Lot numbers | 8353952, 9011582, 9017875, 9024676, 9045702, 9060999, 9079716, 9127571, 9143529, 9156595, 9163601 |
| Model numbers | 306553 |
Product
BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535
Reason for recall
This product has been confirmed to exhibit holes in the packaging, which impacts package integrity and potentially compromises a sterile field.
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-2065-2020. 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.