Beaver-Visitec International Inc.: Medical Device Recall in 2014 - (Recall #: Z-1664-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: May 6, 2014

Date Posted: June 4, 2014

Recall Number: Z-1664-2014

Event ID: 68281

Reason for Recall:

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

Status: Terminated

Product Quantity: 9970 units

Code Information:

Lot number: 3079324

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated