Visitec Anterior Chamber Cannula, .40x22mm (27Gx7/8in) REF 585006 Cannulae are intended to irrigate and or aspirate ophthalmic solutions and liquids in or out of the eye, and remove materials where appropriate. These products are used in all sections of the eye. This cannula is a general use cannula mainly designed for the precise maintenance of optimum anterior chamber depth
FDA Recall Z-1664-2014 · Posted 2014-05-27
Recalling FirmBeaver-Visitec International Inc.
Recall StatusTerminated
Product CodeHMX
Date Initiated2014-05-06
Date Terminated2014-09-05
Product Quantity9970 units
Reason for Recall
Contains a sharp tip needle when the product should contain a blunt tip cannula
Firm Action
Beaver Visitec (BVI) sent a Product Recall Notice dated May 6, 2014, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to immediately return any un-opened product of the affected lot so that BVI can replace the product or issue credit to their company. Customers were asked to fax or email the customer response form to 866-906-4304 or [email protected] as acknowledgement of the letter. Customers with questions should call 781-906-7986.
For questions regarding this recall call 781-906-7950.
Root Cause
Packaging process control
Distribution Pattern
Nationwide Distribution including AL, CT, IN, NC, NY, TX, and VA.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.