FDA Device recall Z-2065-2020
BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535
- FDA Device
- Class II
- terminated
- Published 2020-05-27
On 2020-05-27 the FDA classified a Class II recall of BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535 by Becton Dickinson And, citing this product has been confirmed to exhibit holes in the packaging, which impacts package integrity and potentially compromises a sterile field.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2065-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-04-16 |
| Published | 2020-05-27 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Becton Dickinson And |
| Distribution | US |
Product
BD Posiflush SF Saline Flush Syringe (US Distributed Catalog 306553), UDI 50382903065535
Reason
This product has been confirmed to exhibit holes in the packaging, which impacts package integrity and potentially compromises a sterile field.
Identifiers
| code_info | Lots 8353952 9011582 9017875 9024676 9045702 9060999 9079716 9127571 9143529 9156595 9163601 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2065-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.