ClearanceBrief
Recall Z-1716-2025 ยท HBF Drills, Burrs, Trephines & Accessories (Compound, Powered)

Integra LifeSciences Corp. (NeuroSciences)

CODMAN Disposable Perforator, 14mm. Cranial perforator.

DateMay 6, 2025 (initiated Apr 11, 2025)
StatusOpen, Classified
ReasonInadequate weld that can potentially cause the product to disassemble.
Root causeProcess control
ActionAn URGENT: VOLUNTARY MEDICAL DEVICE RECALL notification, dated 4/11/25, was distributed to consignees via mail and email. Consignees are being asked to check their inventory for affected devices and immediately quarantine any product identified. Consignees are asked to complete the provided Acknowledgement Form and return it via email to FCA3@integralife.com or by fax to 1-609-750-4220; all consignees are to complete and return the form. Integra asks that the recall notification be forwarded to all users of the devices and to customers who received product that was further distributed. Distrib
Quantity170,510 units
DistributionWorldwide distribution - US Nationwide including Puerto Rico and the countries of Argentina, Australia, Austria, Bahamas, Barbados, Belgium, Brazil, Canada, Chile, Colombia, Cyprus, Czechia, Dominican Republic, Ecuador, El Salvador, France, French Guiana, Germany, Ghana, Greece, Hong Kong, India, I
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K183581Codman Disposable Perforators
Integra Lifesciences Corp., Jan 20, 2019