Class II — Becton Dickinson & Company
| Recalling firm | Becton Dickinson and Company |
|---|---|
| Registered facility | View this company's 36 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | BD PAS received customer complaints indicating the absence of the bevel on the non-patient needle end of the product, causing blood leakage. |
| Product | BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608 |
| Quantity | 2,624,160 (2,169,703 US; 454,457 OUS) |
| Distribution | Distributed to accounts in AR, CT, FL, IL, IN, MI, MO, MS, NY, OH, TN, TX, and VA. Foreign distribution to Canada, Brazil, India, Mexico, Singapore, and Taiwan. |
| Initiated | 2019-03-07 |
| Classified | 2019-10-31 |
| Terminated | 2022-02-11 |
| Recall number | Z-0252-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Becton Dickinson & Company (Z-0252-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/82351/
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