Recall Z-0632-2024— Beaver Visitec International, Inc.
Class II · Ongoing
Class II FDA medical device recall by Beaver Visitec International, Inc., initiated 2023-08-25. FDA's recall record names no specific 510(k) clearance for this event. 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..
- Recalling firm
- Beaver Visitec International, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2023-08-25
- Firm location
- Waltham, MA, United States
Product description
Conventional Knife Crescent 2.5mm, 55 degrees bevel up, Part Number 373807
Reason for recall
One lot of Conventional Crescent Knife 2.5mm, 55 degrees bevel-up contains a bevel down blade.
Data sourced from openFDA. This site is unofficial and independent of the FDA.