Z-0374-2026Class I

CODMAN Disposable Perforator 9mm. Cranial Perforator

Name: Z-0374-2026 CODMAN Disposable Perforator 9mm. Cranial Perforator
Creator: Integra LifeSciences Corp. (NeuroSciences)
Published: 2025-09-26
License: https://open.fda.gov/license/

Integra LifeSciences Corporation / initiated 2025-09-26 / Open, Classified / root cause: manufacturing process

FDA source

Integra LifeSciences Corp. (NeuroSciences) began a recall of CODMAN Disposable Perforator 9mm. Cranial Perforator on 2025-09-26. FDA classified it as Class I and gives the reason as "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". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-0374-2026
Classification: Class I
Status: Open, Classified
Initiated: 2025-09-26
Posted: 2025-11-03
Recalling firm: Integra LifeSciences Corporation
Product: CODMAN Disposable Perforator 9mm. Cranial Perforator.
Product code: HBF Drills, Burrs, Trephines & Accessories (Compound, Powered)
Reason for recall: 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.
Root cause tag: manufacturing process
FDA root cause: Process change control
Action: An URGENT: MEDICAL DEVICE RECALL notification dated 9/26/25 was mailed to consignees. Customers with affected devices are to be immediately removed and quarantined. Customers are to send their completed Acknowledgement Form to [email protected] or by fax at 1-609-750-4220. Forward the recall notification to those who use the product for their awareness. Integra Customer Service will reach out to consignees to facilitate product return. Distributors and Sales Representatives with affected devices are to remove product from further distribution. They are to send their completed Acknowledgement Form to [email protected] or by fax at 1-609-750-4220. Distributors are to create an acknowledgement form from the distributor to their customers and provide them with a copy of the recall notification. Sales Representatives are to receive further directions from Integra Customer Service after their Acknowledgement Form has been received. Consignees with any questions are to call 1-800-654-2873 or email [email protected].
Quantity in commerce: 5,109 units
Distribution: Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Austria, Bahamas, Barbados, Belgium, Brazil, Canada, Chile, Colombia, Cyprus, Czechia, Ecuador, France, French Guiana, Germany, Greece, India, Ireland, Italy, Japan, Jordan, Korea, Lithuania, Mexico, Morrocco, Netherlands, New Zealand, Palestine, State of, Philippines, Portugal, Puerto Rico, Qatar, Republic of North Macedonia, Saudi Arabia, Singapore, Slovenia, South Africa, Spain, Sri Lanka, Sweden, Switzerland, Taiwan , Thailand, Trinidad and Tobago, Tunisia, Turkey, United Arab Emirates, United Kingdom of Great Britain and Northern Ireland, Vietnam.
Product codes and lots: Model No. 261223; UDI: 10381780513605; Lot No. 5828553, 6264478, 6264481, 6264482, 7230672, 7230673, 7230674, 7230675, 7261971, 7268008, 7268009, 7268010, 7268011, 7268012, 7268013, 7268014, 7268015, 7268016, 7268017, 7268018, 7268019, 7282954, 7282955, 7293422, 7293423, 7293424, 7293425, 7293426, 7293427, 7293428, 7300667, 7300668, 7300669, 7300670, 7300672, 7300673, 7300674, 7371082, 7371083, 7379652, 7379922, 7379923, 7379924, 7379926, 7379928, 7379660, 7379925, 7379927, 7450559, 7450560, 7450561, 7450562, 7450563, 7450564, 7450565, 7450566, 7451273, 7451274, 7451275, 7451276, 7451277, 7451278, 7451279; Expiration Date: 2024-03-31 to 2029-07-31.

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0374-2026
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0373-2026	Class I	Ongoing	Voluntary: Firm initiated	2025-11-12	2025-11-03
Z-0374-2026	Class I	Ongoing	Voluntary: Firm initiated	2025-11-12	2025-11-03

Product code HBF

K183581Class IICodman Disposable PerforatorsIntegra Lifesciences Corp. / cleared 2019-01-20

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)