FDA recall Z-1801-2018
Beaver-Visitec International Inc. · Class II · device
Product
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
US Nationwide and Canada
Key facts
- Status
- Terminated
- Initiation date
- 2018-02-26
- Report date
- 2018-05-16
- Termination date
- 2019-10-30
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Waltham, MA, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1801-2018