FDA Device recall Z-1801-2018
Wet-Field Hemostatic Eraser Bipolar 25G, fine tip, straight, 5/SP
- FDA Device
- Class II
- terminated
- Published 2018-05-16
On 2018-05-16 the FDA classified a Class II recall of Wet-Field Hemostatic Eraser Bipolar 25G, fine tip, straight, 5/SP by Beaver Visitec International, citing products were packaged with incorrect labeling,.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1801-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-02-26 |
| Published | 2018-05-16 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Beaver Visitec International |
| Distribution | US |
Product
Wet-Field Hemostatic Eraser Bipolar 25G, fine tip, straight, 5/SP; Part Number 221267; UDI: 30886158010549
Reason
Products were packaged with incorrect labeling,
Identifiers
| code_info | Lot number: 6001035 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1801-2018%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.