FDA Adverse Event Malfunction Summary report: N

1.1MM TW DRILL FOR 1.50MM SCR

MDR report key: 3240376 · Received July 17, 2013

Report

Report Number
1045834-2013-03356
Event Type
Malfunction
Date Received
July 17, 2013
Date of Event
June 1, 2013
Report Date
June 17, 2013
Manufacturer
DEPUY SYNTHES POWER TOOLS
Product Code
HBC
PMA / PMN Number
K011444
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SZ
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE ACTUAL DEVICE WAS RETURNED FOR EVAL. RELIABILITY ENGINEERING EVALUATED THE DEVICE AND OBSERVED IF ADD'L INFO SHOULD BECOME AVAILABLE, A SUPPLEMENTAL MEDWATCH REPORT WILL BE SENT ACCORDINGLY.

Description of Event or Problem · 1

IT WAS REPORTED FROM (B)(6) THAT DURING INCOMING INSPECTION, IT WAS OBSERVED THAT THERE WAS "RESIDUE IN THE STERILE PACKAGE" OF THE DEVICE. THE DEVICE WAS NOT USED IN SURGERY. NO INJURIES OF MEDICAL INTERVENTION WERE REPORTED. THE EXACT DATE OF THE EVENT WAS UNK. ALTHOUGH THE REPORTER CLARIFIED THE EVENT OCCURRED IN (B)(6) 2013. ALL AVAILABLE INFO HAS BEE DISCLOSED. IF ADD'L INFO SHOULD BECOME AVAILABLE, A SUPPLEMENTAL MEDWATCH REPORT WILL BE SUBMITTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
331175 1.1MM TW DRILL FOR 1.50MM SCR HBC DEPUY SYNTHES POWER TOOLS F493072383

Patients

Seq Age Sex Outcome Treatment
1