Aspiration Syringe Kit — Class II medical device recall Z-0202-2022
Terminated recall by MICROVENTION INC., reported 2021-11-10, distributed nationwide. Syringe Kits labeled for distribution OUS were inadvertently shipped to US customers.
| Recall number | Z-0202-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | MICROVENTION INC., Aliso Viejo, CA, United States |
| Recall initiated | 2021-10-20 |
| Classified | 2021-11-04 |
| Reported by FDA | 2021-11-10 |
| Terminated | 2024-05-15 |
| Distributed | Nationwide (US) |
| Quantity | 33 |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00816777025906 |
| Lot numbers | H2146461 |
| Model numbers | MVSK60 |
Product
Aspiration Syringe Kit, REF: MVSK60
Reason for recall
Syringe Kits labeled for distribution OUS were inadvertently shipped to US customers.
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-0202-2022. 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.