Health product recall

Codman® Disposable Perforator

Last updated

Summary

Product
Codman® Disposable Perforator
Issue
Medical devices - Performance
What to do

Contact the manufacturer if you require additional information

Audience
Healthcare

Affected products

Affected products Lot or serial number Model or catalogue number
Codman® Disposable Perforator More than 10 numbers, contact manufacturer. 26-1221
Codman® Disposable Perforator More than 10 numbers, contact manufacturer. 26-1222
Codman® Disposable Perforator More than 10 numbers, contact manufacturer. 26-1223

Issue

On April 2025, Integra issued a voluntary recall for the 14mm Codman® Disposable Perforators due to an inadequate weld (proud weld) on specific lots of 14mm Codman® Disposable Perforators that can potentially cause the product to disassemble (break/separate). 

To date, there have been no complaints or adverse events reported in relation to the 9mm and 11mm Codman® Disposable Perforators disassembly.  Out of an abundance of caution, as the 9 and 11 mm perforators are manufactured using the same equipment and operating parameters that affected the 14mm Perforator, Integra has made the decision to expand the scope of the field action to include the 9mm and 11mm perforators.

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Neurology
Companies
Integra Lifesciences Production Corporation
11 Cabot Blvd., Mansfield, Massachusetts, United States, 02048
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-77368

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