Recall Z-2784-2024— Beaver Visitec International, Inc.
Class II · Ongoing
Class II FDA medical device recall by Beaver Visitec International, Inc., initiated 2024-07-26. FDA's recall record names no specific 510(k) clearance for this event. Product: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 584550;. Reason: Data in RES..
- Recalling firm
- Beaver Visitec International, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-07-26
- Firm location
- Waltham, MA, United States
Product description
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 584550;
Reason for recall
Data in RES.
Data sourced from openFDA. This site is unofficial and independent of the FDA.