Recall Z-0633-2024— Beaver Visitec International, Inc.
Class II · Ongoing
Class II FDA medical device recall by Beaver Visitec International, Inc., initiated 2023-10-10. FDA's recall record names no specific 510(k) clearance for this event. Product: Xstar Kojo Safety Slit Knife, 2.5mm 45¿ Bevel Up, Part Number 373025. Reason: One lot of Part Number 373025, Xstar¿ Kojo Safety Slit Knife 2.5mm 45¿ bevel up, incorrectly contains a bevel down blade instead of a bevel up blade..
- Recalling firm
- Beaver Visitec International, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2023-10-10
- Firm location
- Waltham, MA, United States
Product description
Xstar Kojo Safety Slit Knife, 2.5mm 45¿ Bevel Up, Part Number 373025
Reason for recall
One lot of Part Number 373025, Xstar¿ Kojo Safety Slit Knife 2.5mm 45¿ bevel up, incorrectly contains a bevel down blade instead of a bevel up blade.
Data sourced from openFDA. This site is unofficial and independent of the FDA.