MAUDE Adverse Event Report: Stryker Instruments-a division of Stryker Corp ZYPHR DISP CRAN PERF LRG 14/11; Drills, burrs, trephines & accessories

Catalog Number	5100060001
Medical Device Problem Code	Failure to Auto Stop (2938)
Health Effect - Clinical Code	Rupture (2208)
Date of Event	05/14/2026
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
H6: a follow up report will be sent when the investigation is complete.
Event or Problem Description
It was reported that, during surgery, the perforator did not stop appropriately upon reaching the inner table of the skull.It went through and penetrated the dura.It was also reported that the procedure was completed successfully without a clinically significant delay.
Event or Problem Description
No new information.
Additional Manufacturer Narrative
H6: the quality investigation is complete.

• Brand Name: ZYPHR DISP CRAN PERF LRG 14/11
• Common Device Name: Drills, burrs, trephines & accessories
• Manufacturer (Section D): Stryker Instruments-a division of Stryker Corp; 1941 stryker way; portage MI 49002
• Manufacturer (Section G): Stryker Instruments-Ireland; instruments division; carrigtwohill bus. & tech park; carrigtwohill MI NA ; EI NA
• Manufacturer Contact: kelsey barla ; 1941 stryker way; portage, MI 49002 ; +1(269)323-7700
• MDR Report Key: 25234262
• Report Number: 3015967359-2026-00359
• Device Sequence Number: 10357347
• Product Code: HBF
• UDI-Device Identifier: 04546540716224
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K082010
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 09/30/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Catalogue Number: 5100060001
• Device Lot Number: 25123047
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 05/16/2026
• Supplement Date Received by Manufacturer: 09/29/2026
• Initial Report FDA Received Date: 05/20/2026
• Supplement Report FDA Received Date: 09/30/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 05/08/2025
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown