FDA Device recall Z-0632-2024
Conventional Knife Crescent 2.5mm, 55 degrees bevel up, Part Number 373807
- FDA Device
- Class II
- ongoing
- Published 2024-01-10
On 2024-01-10 the FDA classified a Class II recall of Conventional Knife Crescent 2.5mm, 55 degrees bevel up, Part Number 373807 by Beaver Visitec International, citing one lot of Conventional Crescent Knife 2.5mm, 55 degrees bevel-up contains a bevel down blade.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0632-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-08-25 |
| Published | 2024-01-10 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Beaver Visitec International |
| Distribution | n/a |
Product
Conventional Knife Crescent 2.5mm, 55 degrees bevel up, Part Number 373807
Reason
One lot of Conventional Crescent Knife 2.5mm, 55 degrees bevel-up contains a bevel down blade.
Identifiers
| code_info | UDI-DI: 30886158000571; Lot Number: 6054027 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0632-2024%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.