BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 23G x 1 — Class II medical device recall Z-2749-2017
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-2749-2017 |
|---|---|
| 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 | 57,600 units |
| Reason classes | sterility |
| Model numbers | 309571 |
Product
BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 23G x 1 (0.6mm x 25mm) Catalog #309571 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.
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-2749-2017. 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.