Alcon Research, Ltd.: Medical Device Recall in 2015 - (Recall #: Z-0195-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Custom Pak 9319-27. Single-use medical devices and accessories designed by medical professionals for a specific ophthalmic surgical procedure.

Product Classification:

Class II

Date Initiated: September 21, 2015

Date Posted: November 11, 2015

Recall Number: Z-0195-2016

Event ID: 72363

Reason for Recall:

The recalled lot of custom paks are labeled as latex free and contain latex gloves rather than the specified non-latex gloves.

Status: Terminated

Product Quantity: 5 units

Code Information:

1792733H, 1783925H, 1785227H, 1786729H

Distribution Pattern:

Distributed in VT.

Voluntary or Mandated:

Voluntary: Firm initiated