Product Wiki · Recalls · U.S. FDA — Device Enforcement

CODMAN Disposable Perforator 11mm. Cranial Perforator. — recall Z-0373-2026

U.S. FDA — Device Enforcement · United States · 2025-09-26 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0373-2026
Date of alert
2025-09-26
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Integra LifeSciences Corp. (NeuroSciences)
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10381780513612
Reported risk: 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.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.