FDA Device recall Z-0500-2020
BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306575 (Canada only)
- FDA Device
- Class II
- terminated
- Published 2019-11-27
On 2019-11-27 the FDA classified a Class II recall of BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306575 (Canada only) by Becton Dickinson And, citing limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with standard BD Posiflush Pre-Filled Normal Saline Syringes.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0500-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-10-14 |
| Published | 2019-11-27 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Becton Dickinson And |
| Distribution | US |
Product
BD Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306575 (Canada only)
Reason
Limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with standard BD Posiflush Pre-Filled Normal Saline Syringes.
Identifiers
| code_info | Lot Number: 9175971 UDI: 50382903065757 |
|---|
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-0500-2020%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.