BD Needle 22GA 1-1/2in SafetyGlide — Class II medical device recall Z-3116-2017
Terminated recall by Becton Dickinson & Company, reported 2017-09-20, distributed in CA, IL, KS, MI, NC, NY, PA, SC…. Presence of loose polypropylene foreign matter above release specification.
| Recall number | Z-3116-2017 |
|---|---|
| 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 | 2017-06-13 |
| Classified | 2017-09-11 |
| Reported by FDA | 2017-09-20 |
| Terminated | 2020-06-22 |
| Distributed | CA, IL, KS, MI, NC, NY, PA, SC, TX, VA |
| Quantity | 1,249,200 units |
| Reason classes | foreign material |
| Lot numbers | 5268868, 6154760, 6154765, 6211579, 6271695 |
| Model numbers | 301701 |
Product
BD Needle 22GA 1-1/2in SafetyGlide(TM) Non Sterile, Bulk, REF 301701 The BD SafetyGlide(TM) needle is intended to be used for general purpose injection, aspiration of fluids from parts of the body below the surface of the skin, injection into intravenous ports and tubings external to the patient. The needle stick prevention feature of the device contains a mechanism that covers the needlepoint after use. Bulk Non Sterile configuration is intended for further manufacturing, processing or repackaging
Reason for recall
Presence of loose polypropylene foreign matter above release specification.
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-3116-2017. 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.