FDA Device recall Z-0202-2022
Aspiration Syringe Kit, REF: MVSK60
- FDA Device
- Class II
- terminated
- Published 2021-11-10
On 2021-11-10 the FDA classified a Class II recall of Aspiration Syringe Kit, REF: MVSK60 by Microvention, citing syringe Kits labeled for distribution OUS were inadvertently shipped to US customers.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0202-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-10-20 |
| Published | 2021-11-10 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Microvention |
| Distribution | US |
Product
Aspiration Syringe Kit, REF: MVSK60
Reason
Syringe Kits labeled for distribution OUS were inadvertently shipped to US customers.
Identifiers
| code_info | Lot: H2146461; UDI: (01)00816777025906(11)210727(17)240430(10)H2146461 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0202-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.