FDA Adverse Event Injury Summary report: N

DRILL BIT Ø2 W/DOUBLE MARKING L140/115 3

MDR report key: 2869736 · Received December 12, 2012

Report

Report Number
2520274-2012-03825
Event Type
Injury
Date Received
December 12, 2012
Date of Event
March 2, 2010
Report Date
March 5, 2010
Manufacturer
SYNTHES
Product Code
HTW
PMA / PMN Number
EXEMPT
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
PA, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

DEVICE WAS USED FOR TREATMENT. THIS INDIVIDUAL ADVERSE EVENT REPORT IS BEING MADE IN ACCORDANCE WITH THE SYNTHES MDR EXEMPTION REQUEST DATED OCTOBER 2011. A REVIEW OF THE EVENTS ASSOCIATED WITH THE REQUEST WAS PERFORMED AND IT WAS DETERMINED THAT NONE OF THE EVENTS CONSTITUTES SYSTEMIC ISSUES RELATED TO PRODUCT QUALITY, CHANGES IN PRODUCT DESIGN, METHOD OF USE, OR CHANGES IN EXPECTED RISK THRESHOLDS. REVIEW OF THE DATA ALSO INDICATED NO SIGNIFICANT CHANGE IN RISK/BENEFIT OF EACH PRODUCT CATEGORY, NO EVIDENCE OF DEFICIENCIES IN THE DESIGN, LABELING, OR MANUFACTURE OF THE DEVICE. AS NO LOT NUMBER WAS PROVIDED, NO DEVICE HISTORY RECORD REVIEW CAN BE PERFORMED. THE DEVICE IS NOT BEING RETURNED FOR EVALUATION, NO FURTHER INFORMATION IS AVAILABLE ON THIS EVENT. NO FURTHER INVESTIGATION CAN BE PERFORMED.

Description of Event or Problem · 1

THE EU COMPLAINT HANDLING UNIT REPORTED THE DRILL BIT WAS BROKEN DURING USE. THE SURGEON USED THE LOCKING COMPRESSION PLATE DHP ELBOW SYSTEM FOR THE UPPER HUMERUS BONE ON (B)(6). WHILE DRILLING WITH DIAMETER 2.0, APROXIMATELY 30MM WAS BROKEN OFF THE TIP OF THE DRILL BIT AND WAS LEFT IN THE BONE. AFTER THE PLATE REMOVAL, HE USED THE HOLLOW REAMER AND REMOVED IT. HE SAID THAT HE WAS DRILLING CAREFULLY IN THE CORRECT DRILL DIRECTION WITH NO EXTRA FORCE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DRILL BIT Ø2 W/DOUBLE MARKING L140/115 3 LCP ELBOW PLATES HTW SYNTHES

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention