U.S. FOOD AND DRUG ADMINISTRATION: Micro Knife 5.0mm 30


U.S. Food and Drug Administration recently issued the following announcement. 

Date Initiated by Firm: February 19, 2019

Create Date: April 04, 2019

Recall Status: Open, Classified

Recall Number: Z-1088-2019

Recall Event ID: 82248

510(K)Number: K081495  

Product Classification: Knife, ophthalmic - Product Code HNN

Product: 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. .

Code Information: Lot Number 180615

Recalling Firm/Manufacturer: Beaver Visitec

                                                   500 Totten Pond Rd

                                                   10 City Point

                                                   Waltham MA 02451-1916

For Additional Information Contact: Genci Omari

                                                              781-906-6925

Manufacturer Reason

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.

FDA Determined Cause: Error in labeling

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 ClaimsUS@bvimedical.com. 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: ClaimsUS@bvimedical.com or call 866-906-8080 from 8 A.M. to 6 P.M. EST (Monday-Friday).

Quantity in Commerce: 97 boxes (10units/box)

Distribution: US Nationwide Distribution to states of : AL, AZ, CA, FL, ID, MN, MO, NY, OH, PA, and TX; and internationally to: Ireland and UK.

Total Product Life Cycle: TPLC Device Report

Original source can be found here.

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