FDA Device recall Z-0179-2022
BD Syringe Tip Cap Bulk Sterile Convenience Pak-1000 units/shelf carton
- FDA Device
- Class II
- terminated
- Published 2021-11-03
On 2021-11-03 the FDA classified a Class II recall of BD Syringe Tip Cap Bulk Sterile Convenience Pak-1000 units/shelf carton by Becton Dickinson And, citing holes in product packaging impacts package integrity and may compromise sterility.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0179-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-09-27 |
| Published | 2021-11-03 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Becton Dickinson And |
| Distribution | TX |
Product
BD Syringe Tip Cap Bulk Sterile Convenience Pak-1000 units/shelf carton. Used to seal syringes and maintain container closure integrity throughout the shelf life of the BD WWD syringe. Catalog Number: 305822
Reason
Holes in product packaging impacts package integrity and may compromise sterility.
Identifiers
| code_info | Lot Number: 1111347 Exp. Date: 4/30/2026 UDI: 10382903058225 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0179-2022%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.