Acuject Variable Injection Needle — Class II medical device recall Z-2089-2019
Terminated recall by Wilson-Cook Medical Inc., reported 2019-08-07. Potential for occluded injection needles.
| Recall number | Z-2089-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Wilson-Cook Medical Inc., Winston Salem, NC, United States |
| Recall initiated | 2019-06-14 |
| Classified | 2019-07-27 |
| Reported by FDA | 2019-08-07 |
| Terminated | 2021-04-02 |
| Countries outside the US | CN |
| Quantity | 24 |
| UPC / GTIN / UDI-DI | 00827002225268 |
| Lot numbers | W413079 |
| Model numbers | VIN-25 |
| Expiration dates | 2021-10-24 |
Product
Acuject Variable Injection Needle
Reason for recall
Potential for occluded injection needles.
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-2089-2019. 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.