FDA Device recall Z-0252-2020
BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608
- FDA Device
- Class II
- terminated
- Published 2019-11-06
On 2019-11-06 the FDA classified a Class II recall of BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608 by Becton Dickinson And, citing BD PAS received customer complaints indicating the absence of the bevel on the non-patient needle end of the product, causing blood leakage.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0252-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-03-07 |
| Published | 2019-11-06 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Becton Dickinson And |
| Distribution | AR, CT, FL, IL, IN, MI, MO, MS, NY, OH, TN, TX, VA |
Product
BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608
Reason
BD PAS received customer complaints indicating the absence of the bevel on the non-patient needle end of the product, causing blood leakage.
Identifiers
| code_info | Lot 8207894 ***UPDATED 7/11/19*** Lots 9025826 and 8354527 ***UPDATED 12/10/19*** Lot 9010765 |
|---|
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-0252-2020%22
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