OFFSET DOUBLE CLAMP BAR
Report
- Report Number
- 1035617-2009-00009
- Event Type
- Malfunction
- Date Received
- June 12, 2009
- Date of Event
- January 17, 2006
- Report Date
- February 21, 2006
- Manufacturer
- ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS
- Product Code
- HST
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- OTHER
Narratives
ONE SINGLE CLAMP BAR, PRODUCT CODE 00-0640-007-00 AND TWO OFFSET DOUBLE CLAMP BARS, PRODUCT CODE 00-1066-005-00 WERE RETURNED FOR EVALUATION. HOWEVER, IT COULD NOT BE DETERMINED IF THE DEVICES WERE ASSOCIATED WITH THE EVENT REPORTED IN THIS MEDWATCH. VISUAL EXAMINATION REVEALED THAT THE 48" PLAIN BAR CLAMP WAS BROKEN AT THE BASE AND THE SECOND WAS BROKEN AT THE HINGE. THIS MDR IS BEING SUBMITTED LATE, AS IT WAS IDENTIFIED AS PART OF A RETROSPECTIVE REVIEW CONDUCTED BY ZIMMER ORTHOPEDIC SURGICAL PRODUCTS (ZIMMER OSP). THIS RETROSPECTIVE REVIEW WAS CONDUCTED IN RESPONSE TO AN INSPECTIONAL OBSERVATION AT A ZIMMER FACILITY. THE AGENCY'S INSPECTIONAL OBSERVATION CONCERNED THE COMPANY'S DECISION(S) NOT TO SUBMIT CERTAIN MDRS FOR PRODUCTS SPECIFIC TO THAT ZIMMER FACILITY. WHILE A RETROSPECTIVE REVIEW OF COMPLAINTS FOR UNREPORTED MDRS WAS CONDUCTED IMMEDIATELY FOLLOWING THE INSPECTION AT THE FACILITY, ZIMMER DETERMINED THAT SUCH A REVIEW WOULD BE CONDUCTED AT ALL ZIMMER FACILITIES. AS A RESULT, ZIMMER OSP COMPLETED ITS RETROSPECTIVE REVIEW AND IS NOW SUBMITTING THIS MDR.
IT WAS REPORTED THAT A TRAPEZE BROKE AND FELL. THERE WAS NO REPORT OF PT INJURY OR MEDICAL INTERVENTION ASSOCIATED WITH THIS INCIDENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | OFFSET DOUBLE CLAMP BAR | OFFSET DOUBLE CLAMP BAR | HST | ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS | NA | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |