bvi CustomEyes Kit-CustomEyes Cataract Surgical Kits that contain Beaver Xstar Crescent Knife (REF#373809) as a component-non-sterile sample for evaluation purposes REF# BVI 58000587
FDA Recall Z-0230-2022 · Posted None
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Recalling FirmBeaver Visitec International, Inc.
Recall StatusOpen, Classified
Product CodeOJK
Date Initiated2021-10-08
Product Quantity2 units
Reason for Recall
Product packaged as Beaver Xstar Crescent Knife, 2.5mm, 55 degrees bevel-down blades contain bevel-up blades
Firm Action
BVI notified Consignees by Urgent Medical Device Recall letter on 10/8/21 via registered mail. Letter states reason for recall, health risk and action to take:
1. Immediately examine your inventory and quarantine product from these lots that are subject to recall.
If you have further distributed this product, please notify your customers by initiating a subrecall.
Consider all potential users of this product in your user supply chain. You are encouraged to a copy of this recall notification letter when contacting your customers.
2. Complete the enclosed Business Reply Form (BRF) and indicate whether you have affected product to return.
3. Please enter the following information on the enclosed BRF: part number(s), lot number(s) and quantity(ies) of device(s) that are being returned.
4. Return the completed BRF to BVI by one of these methods:
" Fax to 866-552-4919
" Email the attached to [email protected]
5. Return your product to STERICYCLE using the enclosed UPS pre-paid return label:
Stericycle 2670 Executive Drive, Suite A Indianapolis, IN 46241
Attn: Event 3997
If you received this notification without the prepaid UPS label and Business Reply Form (BRF), and require additional shipping labels, or if you have questions regarding the return procedure, please contact Stericycle Inc. at 866-606-8264 (Mon.-Fri. 8:00 am - 5:00 pm Eastern Time).
Please direct any questions regarding this matter to our customer service department by email [email protected] and please include in the subject line: Master Case PIR 263383
Root Cause
Under Investigation by firm
Distribution Pattern
Nationwide Foreign: Australia Austria France Germany Netherlands Spain Japan Russia South Africa UK
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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