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No image published for this recall

Custom-pak™ ophthalmic surgery procedure pack

Official notice

10 Nov 2022

Last checked

10 Nov 2022

Medium riskHealth Canada

An official Health Canada notice concerns Custom-pak™ ophthalmic surgery procedure pack. 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 Published 2022-11-10.

What to do now

Contact the manufacturer if you require additional information.

Recall number

72181

Official notice

2022-11-10

The hazard

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

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Recall Numbers

72181

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Affected products

Product 1

Affected products - Custom-Pak™ Ophthalmic Surgery Procedure Pack, Lot or serial number - More than 10 numbers, contact manufacturer., Model or catalog number - 00000-00 TO 99999-99

Risk / hazard

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

Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

CA · Canada

Affected area 1

CA · Canada

Company & contacts

Manufacturer

Not provided

Phone

Not provided

Brand: Alcon Laboratories, Custom-pak™ Ophthalmic Surgery Procedure Pack.

Source & status

Source

Health Canada

Tier

official

Category

HEALTH

Classification

Type II

App estimate

medium

Recall details

Recall number

72181

Classification

Type II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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