FDA Adverse Event Injury Summary report: N

EXPERT NAIL A2FN Ø13 R CANN L400 TAN LIGHT GR

MDR report key: 2925678 · Received January 22, 2013

Report

Report Number
8030965-2013-00187
Event Type
Injury
Date Received
January 22, 2013
Date of Event
November 22, 2012
Report Date
December 21, 2012
Manufacturer
SYNTHES GMBH
Product Code
HSB
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
SZ
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THIS DEVICE IS USED FOR TREATMENT, NOT DIAGNOSIS. DEVICE IS NOT DISTRIBUTED IN THE UNITED STATES BUT IS SIMILAR TO A DEVICE MARKETED IN THE UNITED STATES. SUBJECT DEVICE HAS BEEN RECEIVED AND IS CURRENTLY IN THE EVALUATION PROCESS. MANUFACTURING DOCUMENTS WERE REVIEWED, AND NO COMPLAINT RELATED ISSUES WERE FOUND.

Additional Manufacturer Narrative · 1

AN INTERNAL INVESTIGATION WAS CONDUCTED AT SYNTHES (B)(4). THE DEVICE PASSED THE REQUIRED FUNCTIONAL TEST SUCCESSFULLY. THE EXTRACTION SCREW CAN BE CONNECTED TO THE NAIL AS INTENDED. WE WERE NOT ABLE TO REPRODUCE THE PROBLEM AS PER EVENT DESCRIPTION. THE MICROSCOPIC INVESTIGATION SHOWS MARGINAL DEFORMATION ON THE THREAD RUN-IN CAUSED DURING THE OPERATION. NO PRODUCT FAULT COULD BE DETECTED.

Description of Event or Problem · 1

DURING SURGERY, IT WAS NOT POSSIBLE TO CONNECT THE EXTRACTION SCREW WITH THE THREAD OF THE EXPERT NAIL. AFTER SEVERAL UNSUCCESSFUL ATTEMPTS, ALSO WITH ANOTHER EXTRACTION SCREW, THE SURGEON USED A HOOKED GUIDING ROD TO REMOVE THE NAIL. THE SURGERY WAS DELAYED 2 HOURS. NO ADDITIONAL MEDICAL TREATMENT WAS REQUIRED. THIS IS # 2 OF 2 REPORTS SUBMITTED ON THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
29019 EXPERT NAIL A2FN Ø13 R CANN L400 TAN LIGHT GR EXPERT NAIL HSB SYNTHES GMBH 3291821

Patients

Seq Age Sex Outcome Treatment
1 17 YR Required Intervention EXACTION SCREW