Official recall record
Codman® Disposable Perforator
- 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.
Record last checked against the registry on 2026-05-31.