FDA Adverse Event Malfunction Summary report: N

LUPINE DRILL BIT

MDR report key: 2062260 · Received March 18, 2011

Report

Report Number
1221934-2011-00125
Event Type
Malfunction
Date Received
March 18, 2011
Date of Event
March 14, 2011
Report Date
March 15, 2011
Manufacturer
DEPUY MITEK
Product Code
HTW
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

NOTHING IS BEING RETURNED FOR EVAL AND NO LOT HAS BEEN IDENTIFIED, WHICH PRECLUDES CONDUCTING A BATCH RECORD REVIEW TO DETERMINE IF THERE WERE ANY INTERNAL PROCESSING ISSUES WHICH WOULD HAVE CONTRIBUTED TO THE NATURE OF THE PRODUCT COMPLAINT. HOWEVER, WE BELIEVE THAT THIS TYPE OF EVENT IS MOST LIKELY TECHNIQUE RELATED, EXTENSIVE LAB TESTING HAS SHOWN THAT UNDER NORMAL CONDITIONS, THE REPORTED EVENT MODE COULD NOT BE DUPLICATED, HOWEVER, UNDER EXTREME CONDITIONS, THAT IS WHEN THE DRILL GUIDE WAS BENT DURING DRILLING WITH A DRILL BIT, THIS CAUSED THE DRILL BIT TO RUB AGAINST INNER SURFACE OF THE BENT DRILL GUIDE CAUSING SOME METAL TO SHAVE OFF OF THE DRILL GUIDE, THE REPORTED CONDITION WAS THEN DUPLICATED. OUTSIDE OF THIS HYPOTHESIS AND CONSIDERATION, WE CANNOT DISCERN ANY OTHER ROOT CAUSE FOR THE REPORTED ISSUE; AT THIS POINT IN TIME, NO CORRECTIVE OR FURTHER ACTION IS WARRANTED.

Description of Event or Problem · 1

OUR REP IS REPORTING TO US THAT DURING AN ARTHROSCOPIC SHOULDER PROCEDURE, THE SURGEON OBSERVED METAL SHAVINGS FALLING INTO THE PT'S BODY WITH THE USE OF A LUPINE DRILL BITS. ALL OF THE DEBRIS WAS REMOVED AND THE PROCEDURE WAS CONCLUDED SUCCESSFULLY WITHOUT FURTHER ISSUE OR HARM TO THE PT. THE COMPLAINT DEVICES WERE DISCARDED AT THE USER FACILITY. THIS HAPPENED IN 2 SEPARATE CASES: SEE ASSOCIATED MDR 1221934-2011-00124.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LUPINE DRILL BIT ARTHROSCOPIC INSTRUMENT HTW DEPUY MITEK 211033 UNK

Patients

Seq Age Sex Outcome Treatment
1 UNK