Micro Knife 5.0mm 30, Part Number 0001522 The Beaver Micro Knife 5.0mm 30 is a sharp pointed tip intended for ophthalmic, ENT and other forms of surgery stab incisions and other microsurgical techniques. .
FDA Recall Z-1088-2019 · Posted None
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Recalling FirmBeaver Visitec
Recall StatusTerminated
Product CodeHNN
Date Initiated2019-02-19
Date Terminated2020-07-21
Product Quantity97 boxes (10units/box)
Reason for Recall
The product contains a misprinted expiration date on the peel pack. Both were printed as "180615", which is the lot
number. The Lot number is correct.
Firm Action
The firm, Beaver-Visitec International, Inc, sent an "URGENT: MEDICAL DEVICE RECALL" notification letter dated 2/19/19 to customers. The letter described the product, problem and actions to be taken. The customers were instructed to do the following:
1. Immediately examine your inventory and quarantine product from this lot subject to recall. If you have further distributed this product, please identify your customers and notify them of this product recall. Consider all potential users of this product in your user supply chain.
2. Complete and return the enclosed Product Recall Notice Response & Return Form IMMEDIATELY, even if you do not have product to return via Fax 866-906-4304 or email a copy to [email protected]. Please include a copy of the completed Response & Return Form with your shipment in the address provided below.
3. Return All quarantined product from the affected lot to our company utilizing the Return Merchandise Authorization sticker label return (Figure 2) that is included in this letter. You may use the prepaid BVI Fed Ex number for your return. Return Merchandise--Beaver- Visitec International, Inc.
Attn: QIC Team- SF74660-0001522; 3550 Roy Orr Blvd. Ste. 180
Grand Prairie, TX 75050. Please use BVI FedEx account 122227600
when shipping the returns back to Grand Prairie.
If you have any specific product replacement questions you may contact our Customer Service Team at: [email protected] or call 866-906-8080 from 8 A.M. to 6 P.M. EST (Monday-Friday).
Root Cause
Error in labeling
Distribution Pattern
US Nationwide Distribution to states of : AL, AZ, CA, FL, ID, MN, MO, NY, OH, PA, and TX; and internationally to: Ireland and UK.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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