Health product recall

Custom-Pak™ Ophthalmic Surgery Procedure Pack

Last updated

Summary

Product
Custom-Pak™ Ophthalmic Surgery Procedure Pack
Issue
Medical devices - Performance issue
What to do

Contact the manufacturer if you require additional information.

Audience
Healthcare
Industry

Affected products

Affected products

Lot or serial number

Model or catalog number

Custom-Pak™ Ophthalmic Surgery Procedure Pack

More than 10 numbers, contact manufacturer.

00000-00 TO 99999-99

Issue

Alcon received notice of a product recall from their vendor, 3M, regarding their 3M Steri-drape™ surgical drapes, which are included in specific lots of Alcon Custom Pak®. The reason of this recall is due to difficulty removing the liner on the adhesive component of the affected drapes without damaging the product and may render the product unusable. To date, Alcon has not received any report of patient or user harm related to this issue.

Recall start date: October 28, 2022

Additional information

Details
Original published date: 2022-11-10
Alert / recall type
Health product recall
Category
Health product - Medical device - General hospital and personal use
Companies

Alcon Laboratories Inc.

6201 South Freeway, Fort Worth, Texas, United States, 76134-2099

Published by
Health Canada
Audience
Healthcare
Industry
Recall class
Type II
Identification number
RA-72181