Z-0202-2022 Class II Terminated
FDA device recall Z-0202-2022 was initiated by MICROVENTION INC. on October 20, 2021 and is designated Class II. Reason for recall: Syringe Kits labeled for distribution OUS were inadvertently shipped to US customers. The recall status is terminated (terminated May 15, 2024). Affected quantity: 33.
Recall Details
- Product Type
- Devices
- Report Date
- November 10, 2021
- Initiation Date
- October 20, 2021
- Termination Date
- May 15, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 33
Product Description
Aspiration Syringe Kit, REF: MVSK60
Reason for Recall
Syringe Kits labeled for distribution OUS were inadvertently shipped to US customers.
Distribution Pattern
US Nationwide distribution in the states of AL, NY, NV.
Code Information
Lot: H2146461; UDI: (01)00816777025906(11)210727(17)240430(10)H2146461