Z-1030-2022 Class II Terminated
FDA device recall Z-1030-2022 was initiated by Acera Surgical Inc on March 21, 2022 and is designated Class II. Reason for recall: Misprinted expiration date on the shelf-box The recall status is terminated (terminated August 20, 2024). Affected quantity: 83 units.
Recall Details
- Product Type
- Devices
- Report Date
- May 11, 2022
- Initiation Date
- March 21, 2022
- Termination Date
- August 20, 2024
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 83 units
Product Description
Restrata, Part Number RWM1-2X2
Reason for Recall
Misprinted expiration date on the shelf-box
Distribution Pattern
Nationwide
Code Information
Lot Number 51745 UDI (01) 8 52425800 60682 (10) 51745 (17) 220218 (21) 0068