HomeMedical Device recalls
High severity

CODMAN Disposable Perforator 9mm. Cranial Perforator.

SourceFDA Device Enforcement
CategoryMedical Device
SeverityHigh
Statusongoing
Recall dateSeptember 26, 2025
ReportedNovember 12, 2025
Recalling firmIntegra LifeSciences Corp. (NeuroSciences)
Country / regionUnited States NJ

Hazard

Expansion of recall of size 14 mm Codman Disposable Perforators for inadequate welds to size 11 mm and 9 mm Codman Disposable Perforators out of an abundance of caution.

Affected products

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