FDA Device recall Z-3116-2017
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 purpo…
- FDA Device
- Class II
- terminated
- Published 2017-09-20
On 2017-09-20 the FDA classified a Class II recall of 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 purpo… by Becton Dickinson And, citing presence of loose polypropylene foreign matter above release specification.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3116-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-06-13 |
| Published | 2017-09-20 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Becton Dickinson And |
| Distribution | CA, IL, KS, MI, NC, NY, PA, SC, TX, VA |
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
Presence of loose polypropylene foreign matter above release specification.
Identifiers
| code_info | Lot Numbers: 6211579, 6271695, 6154760, 6154765 & 5268868 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3116-2017%22
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