Recall Z-1200-2023— Beaver Visitec International, Inc.
Class II · Ongoing
Class II FDA medical device recall by Beaver Visitec International, Inc., initiated 2022-12-20. FDA's recall record names no specific 510(k) clearance for this event. Product: CustomEyes kits. Reason: Device packaging may contain open seals, compromising product sterility..
- Recalling firm
- Beaver Visitec International, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2022-12-20
- Firm location
- Waltham, MA, United States
Product description
CustomEyes kits
Reason for recall
Device packaging may contain open seals, compromising product sterility.
Data sourced from openFDA. This site is unofficial and independent of the FDA.