FDA Device recall Z-0444-2016
Unolok Blunt Fill Needle 18G x 1.5" Red, Sterile, Single use, Non-injectable needle, Single use, non-injection needle
- FDA Device
- Class II
- terminated
- Published 2015-12-23
On 2015-12-23 the FDA classified a Class II recall of Unolok Blunt Fill Needle 18G x 1.5" Red, Sterile, Single use, Non-injectable needle, Single use, non-injection needle by Myco Medical Supplies, citing particulates: Complaints of rubber coring from the closure of injection vials.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0444-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-11-06 |
| Published | 2015-12-23 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Myco Medical Supplies |
| Distribution | US |
Product
Unolok Blunt Fill Needle 18G x 1.5" Red, Sterile, Single use, Non-injectable needle, Single use, non-injection needle
Reason
Particulates: Complaints of rubber coring from the closure of injection vials.
Identifiers
| code_info | Item #02463, Lot numbers: 19351R, 16561M, 17531D, 22541D, 22551D, 25551D and 25551M. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0444-2016%22
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