(1)VitreQ 25G BF Blunt Needles-BF25.D51 GITN: 8719214221164 (2)… — Class II medical device recall Z-0847-2020
Terminated recall by Vitreq Bv, reported 2020-02-05, distributed nationwide. Microscopic tears of the sterile pouch may compromise sterility
| Recall number | Z-0847-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Vitreq Bv, Vierpolders, N/A, Netherlands |
| Recall initiated | 2019-12-17 |
| Classified | 2020-01-24 |
| Reported by FDA | 2020-02-05 |
| Terminated | 2020-12-09 |
| Distributed | Nationwide (US) |
| Reason classes | sterility |
| UPC / GTIN / UDI-DI | 08719214221164, 08719214221188 |
Product
(1)VitreQ 25G BF Blunt Needles-BF25.D51 GITN: 8719214221164 (2) VitreQ 25G BF Brush Needles-BF25.D52 GTIN: 8719214221188
Reason for recall
Microscopic tears of the sterile pouch may compromise sterility
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-0847-2020. 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.