FDA Recall Open, Classified

Xstar Safety Slit Knife, 2.75 mm 45 Bevel Up, Model Number 378227, a component of CustomEye Kits, Numbers 584562, 5800109

Recall: Z-2162-2024 · Initiated May 10, 2024

Recall

Recall Number
Z-2162-2024
Event Number
94645
Firm
Beaver Visitec International, Inc.
FEI Number
1211998
Product Code
HNN
Status
Open, Classified
Root Cause
Process control
Initiated
May 10, 2024
Posted
June 20, 2024
Address
500 Totten Pond Rd, 10, City Point Waltham, MA, 02451-1916

Description

Xstar Safety Slit Knife, 2.75 mm 45 Bevel Up, Model Number 378227, a component of CustomEye Kits, Numbers 584562, 5800109

Reason

The wrong configuration of the blade was in the package. The bevel was on the opposite side, instead of being in front (bevel up) it was in the back (bevel down).

Action

An URGENT Field Safety Notice dated 5/10/24 was sent to customers. Actions Required by You Our records show you received one or more affected product. You can recognize the affected product by determining whether the lot number printed on the device label is one of the affected lots. PLEASE perform the following actions: 1. Immediately examine your inventory and determine if the blades on the knives are bevel-up as intended or bevel down. In case you purchased the CustomEye Kit please be advised it is not possible to check the bevel orientation without losing the KIT sterility. In such case, immediately put the KIT out of use. 2. In case a non-conforming product is identified please quarantine it and return ALL quarantined product from the affected lots to our company via pre-paid postal labels, supplied to you with an initial notification 3. If you have further distributed this product, please notify your customers by initiating a sub-recall. Consider all potential users of this product in your user supply chain. You are encouraged to use a copy of this recall notification letter when contacting your customers. 4. Review the enclosed Business Reply Form (BRF) and indicate whether you have the affected product in your possession. 5. Please enter the following information on the enclosed BRF: part number(s), lot number(s) and quantity(ies) of device(s) destroyed. 6. Return the completed BRF to BVI by emailing the attached to [email protected] (U.S based customers) or to [email protected] (rest of the world based customers). BVI values your business and apologizes for the inconvenience this may have caused. Please direct any questions regarding credit to our customer service department by email and include in the subject line: Master Case PIR 00564835. Country Customer Service Email UK [email protected] FR [email protected] DE/ AT [email protected] IT [email protected] ROW ROWCustomerSupport@bvimedical

Distribution

Worldwide distribution - US Nationwide and the countries of Canada, UK, and Italy.

Quantity

126 units