RecallDepth

BVI Custom Eyes Ophthalmic Procedure Kits with the component -Devon Light Glove Part Number: 584649 Ophthalmic surgical kits

This recall has been terminated (originally issued June 15, 2015).

Company
Beaver-Visitec International Inc.
Recall Initiated
May 1, 2015
Posted
June 15, 2015
Terminated
January 28, 2021
Recall Number
Z-1804-2015
Quantity
585 kits
Firm Location
Waltham, MA
Official Source
View on FDA website ↗

Reason for Recall

Devon Light Glove in procedure kits may have holes/slits compromising sterility of the product

Distribution

Nationwide Distribution including KY, GA, MI, and NJ.

Lot / Code Info

Lot Numbers:  3039720 3046211 3047770 3049473 3070763 3082330 3089827 3093682 3095941 3106407 3117874

Root Cause

Nonconforming Material/Component

Action Taken

Beaver-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.

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