Beaver-Visitec International Inc. recalls Visitec Anterior Chamber Cannula, .40x22mm (27Gx7/8in) REF 585006 Cannulae are intended to irrigate and or aspirate

Recalled June 4, 2014 · FDA recall Z-1664-2014 · Beaver-Visitec International

Hazard

Contains a sharp tip needle when the product should contain a blunt tip cannula · FDA Class II

Units

9970 units

Sold at

Nationwide Distribution including AL, CT, IN, NC, NY, TX, and VA.

Description

Contains a sharp tip needle when the product should contain a blunt tip cannula

Product

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

Manufacturer(s)

Beaver-Visitec International Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →