Unolok Blunt Fill Needle 18G x 1 — Class II medical device recall Z-0444-2016
Terminated recall by Myco Medical Supplies Inc, reported 2015-12-23, distributed nationwide. Particulates: Complaints of rubber coring from the closure of injection vials.
| Recall number | Z-0444-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Myco Medical Supplies Inc, Cary, NC, United States |
| Recall initiated | 2015-11-06 |
| Classified | 2015-12-17 |
| Reported by FDA | 2015-12-23 |
| Terminated | 2017-05-03 |
| Distributed | Nationwide (US) |
| Reason classes | specification failure |
| Lot numbers | 16561M, 17531D, 19351R, 22541D, 22551D, 25551D, 25551M |
| Model numbers | 02463 |
Product
Unolok Blunt Fill Needle 18G x 1.5" Red, Sterile, Single use, Non-injectable needle, Single use, non-injection needle
Reason for recall
Particulates: Complaints of rubber coring from the closure of injection vials.
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-0444-2016. 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.