Z-1801-2018 Class II Terminated
FDA device recall Z-1801-2018 was initiated by Beaver-Visitec International Inc. on February 26, 2018 and is designated Class II. Reason for recall: Products were packaged with incorrect labeling, The recall status is terminated (terminated October 30, 2019). Affected quantity: 1025.
Recall Details
- Product Type
- Devices
- Report Date
- May 16, 2018
- Initiation Date
- February 26, 2018
- Termination Date
- October 30, 2019
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 1025
Product Description
Wet-Field Hemostatic Eraser Bipolar 25G, fine tip, straight, 5/SP; Part Number 221267; UDI: 30886158010549
Reason for Recall
Products were packaged with incorrect labeling,
Distribution Pattern
US Nationwide and Canada
Code Information
Lot number: 6001035