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U.S. Department of Health and Human Services

Class 2 Device Recall Beaver Visitec

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 Class 2 Device Recall Beaver Visitecsee related information
Date Initiated by FirmMay 01, 2015
Date PostedJune 15, 2015
Recall Status1 Terminated 3 on January 28, 2021
Recall NumberZ-1805-2015
Recall Event ID 71293
Product Classification Light, surgical, ceiling mounted - Product Code FSY
ProductBVI Custom Eyes Ophthalmic Procedure Kits with the component -Devon Light Glove Part Number: 584671 Ophthalmic surgical kits
Code Information Lot Numbers:  3045852 3053258 3063193 3068829 
Recalling Firm/
Manufacturer		 Beaver-Visitec International Inc.
411 Waverley Oaks Rd Ste 229
Waltham MA 02452-8422
For Additional Information ContactSAME
781-906-7950
Manufacturer Reason
for Recall		Devon Light Glove in procedure kits may have holes/slits compromising sterility of the product
FDA Determined
Cause 2		Nonconforming Material/Component
ActionBeaver-Visitec International Sales Ltd. (BVI) sent an Urgent Field Safety Notice dated May 2, 2015, to all affected customers. Customers were instructed to quarantine the affected kits and return to BVI for subsequent replacement of product. A Verification Form was provided to confirm receipt of the recall notice. For questions regarding this recall call 791-906-7950.
Quantity in Commerce214 kits
DistributionNationwide Distribution including KY, GA, MI, and NJ.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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