Class II — MICROVENTION INC.
| Recalling firm | MicroVention Inc. |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Syringe Kits labeled for distribution OUS were inadvertently shipped to US customers. |
| Product | Aspiration Syringe Kit, REF: MVSK60 |
| Quantity | 33 |
| Distribution | US Nationwide distribution in the states of AL, NY, NV. |
| Initiated | 2021-10-20 |
| Classified | 2021-11-04 |
| Terminated | 2024-05-15 |
| Recall number | Z-0202-2022 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — MICROVENTION INC. (Z-0202-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/88892/
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