BD Vacutainer Eclipse Blood Collection Needles 22Gx1 — Class II medical device recall Z-0252-2020
Terminated recall by Becton Dickinson & Company, reported 2019-11-06, distributed in AR, CT, FL, IL, IN, MI, MO, MS…. BD PAS received customer complaints indicating the absence of the bevel on the non-patient needle end of the p
| Recall number | Z-0252-2020 |
|---|---|
| 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 | 2019-03-07 |
| Classified | 2019-10-31 |
| Reported by FDA | 2019-11-06 |
| Terminated | 2022-02-11 |
| Distributed | AR, CT, FL, IL, IN, MI, MO, MS, NY, OH, TN, TX, VA |
| Countries outside the US | BR, CA, IN, MX, SG, TW |
| Reason classes | packaging |
| Lot numbers | 8207894, 8354527, 9010765, 9025826 |
| Model numbers | 368608 |
Product
BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608
Reason for recall
BD PAS received customer complaints indicating the absence of the bevel on the non-patient needle end of the product, causing blood leakage.
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-0252-2020. 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.