BD 3ml Syringe Luer-Lok" Tip Catalog 309657 The BD Single Use — Class II medical device recall Z-2751-2017
Terminated recall by Becton Dickinson & Company, reported 2017-07-26, distributed nationwide. BD identified that several lots did not receive the specified dose of irradiation necessary to meet the Steril
| Recall number | Z-2751-2017 |
|---|---|
| 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 | 2016-09-16 |
| Classified | 2017-07-19 |
| Reported by FDA | 2017-07-26 |
| Terminated | 2018-03-20 |
| Distributed | Nationwide (US) |
| Quantity | 648,000 units |
| Reason classes | sterility |
| Model numbers | 309657 |
Product
BD 3ml Syringe Luer-Lok" Tip Catalog 309657 The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injection
Reason for recall
BD identified that several lots did not receive the specified dose of irradiation necessary to meet the Sterility Assurance Level (SAL) required of 10-6.
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-2751-2017. 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.