ProductGuru Recalls

Official recall record

Codman® Disposable Perforator

Health Canada — Medical Devices · 2025-04-30 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2025-04-30
Last updated (per notice)
2025-10-22
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

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.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

Verify at the source: Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.

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