Cooper Vision Caribbean Corp.: Medical Device Recall in 2013 - (Recall #: Z-0631-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

AVAIRA (enfilcon A) Soft (Hydrophilic) Daily Wear Toric Contact Lenses

Product Classification:

Class II

Date Initiated: November 9, 2012

Date Posted: January 9, 2013

Recall Number: Z-0631-2013

Event ID: 63719

Reason for Recall:

The lenses exceeded the acceptance limit for silicone oil residual.

Status: Terminated

Product Quantity: 246

Code Information:

10447500016006, 10519550007006, 10537500016014

Distribution Pattern:

US Nationwide, including Puerto Rico, and Canada.

Voluntary or Mandated:

Voluntary: Firm initiated