FDA Logo links to FDA home pageCenter for Devices and Radiological Health, U.S. Food and Drug AdministrationHHS Logo links to Department of Health and Human Services website

FDA Home Page | CDRH Home Page | Search | CDRH A-Z Index | Contact CDRH U.S. Food and Drug Administration Center for Devices and Radiological Health [Skip navigation]
horizonal rule

Super Search
510(k) | Registration & Listing | Adverse Events | PMA | Classification | CLIA
CFR Title 21 | Advisory Committees | Assembler | Recalls | Guidance | Standards
 

 

Adverse Event Report

DEPUY ORTHOPAEDICS, INC./DEPUY A JOHNSON & JOHNSON CO DEPUY CURETTE 10 MM   back to search results
Model Number 6020-11
Patient Outcome  Other;
Event Description

Add'l info rec'd from mfr 8/20/04: the product was not returned for the subject complaint. Therefore, physical examination was not possible. The product lot number was not provided so review of the device history was not possible. If the product was returned, hardness or destructive testing could have been performed. In addition, the instrument could have been microscopically evaluated to possibly determine how the tip fractured. A search of the complaint database revealed two prior reports of breakage for this instrument. The first report was received on august 11, 2000. Although the complaint was confirmed, it was attributed to heavy usage based on the overall cosmetic appearance of the instrument. The second report was received on march 13, 2003. The instrument was discarded and the lot number was not recorded. Therefore, the investigation could not verify or draw any conclusions about the reported event. Complaint trends for this instrument will continue to be monitored to determine if corrective action is indicated.

 
Event Description

Procedure performed: revision left femoral component, depuy, with a new depuy porous coated long stem with associated bone grafting with agf and crotons. During surgical procedure, a depuy 10mm curette from the revision tray instrument set, was being used to remove a large piece of cement when a small portion of the end of the instrument broke/knocked off in the femoral canal. It was not possible for the surgeon to remove the small piece. Many valiant attempts were made, but it was determined that it would be in the pt's best interest to discontinue further attempts to retrieve the portion. The surgeon did not want to make a window in the bone which would weaken the bone.

 
Search Alerts/Recalls

  new search  |  submit an adverse event report

Brand NameDEPUY
Type of DeviceCURETTE 10 MM
Baseline Device 510(K) Number
Baseline Device PMA Number
Manufacturer (Section D)
DEPUY ORTHOPAEDICS, INC./DEPUY A JOHNSON & JOHNSON CO
700 orthopaedic dr
p.o. box 988
warsaw IN 46581 0988
Device Event Key522833
MDR Report Key533562
Event Key506597
Report NumberMW1032365
Device Sequence Number1
Product CodeFZS
Report Source Voluntary
Report Date 06/08/2004
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received06/08/2004
Is This An Adverse Event Report? No
Is This A Product Problem Report? Yes
Device Operator Health Professional
Device MODEL Number6020-11
Was Device Available For Evaluation? No
Is the Device an Implant? No
Is this an Explanted Device? No Answer Provided

Database last updated on February 28, 2009

horizonal rule

CDRH Home Page | CDRH A-Z Index | Contact CDRH | Accessibility | Disclaimer
FDA Home Page | Search FDA Site | FDA A-Z Index | Contact FDA | HHS Home Page

Center for Devices and Radiological Health / CDRH