FDA Adverse Event Injury Summary report: N

UNKNOWN ZIMMER TIBIAL BASEPLATE

MDR report key: 1924219 · Received December 7, 2010

Report

Report Number
1822565-2010-01275
Event Type
Injury
Date Received
December 7, 2010
Date of Event
March 23, 2004
Report Date
November 4, 2010
Manufacturer
ZIMMER INC.
Product Code
HSH
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

INFO WAS REC'D FROM PFIZER, INC.EVAL SUMMARY: NO DEVICES OR PHOTOS WERE REC'D; THEREFORE, THE CONDITION OF THE COMPONENTS IS UNK. SURGICAL NOTES WERE PROVIDED, BUT PROVIDED LIMITED INFO. X-RAYS WERE NOT PROVIDED; IT IS UNK WHETHER THE COMPONENTS WERE IMPLANTED WITH THE CORRECT FIT AND ORIENTATION AS PER THE SURGICAL TECHNIQUE. PT FACTORS THAT MAY AFFECT THE PERFORMANCE OF THE COMPONENTS SUCH AS AGE, BONE QUALITY, HEIGHT, WEIGHT, ACTIVITY LEVEL, TYPE OF ACTIVITY (LOW IMPACT VS. HIGH IMPACT) ARE UNK. A DEFINITIVE ROOT CAUSE CANNOT BE DETERMINED WITH THE INFO PROVIDED. EVAL CODES: REVIEW OF THE DEVICE HISTORY RECORDS WAS NOT POSSIBLE AS THE PRODUCT AND/OR LOT NUMBERS REQUIRED FOR RETRIEVAL WERE UNAVAILABLE. IT IS NOT SUSPECTED THAT THE PRODUCT FAILED TO MEET SPECIFICATIONS. THE INVESTIGATION COULD NOT VERIFY OR IDENTIFY ANY EVIDENCE OF PRODUCT CONTRIBUTION TO THE REPORTED PROBLEM. BASED ON THE AVAILABLE INFO, THE NEED FOR CORRECTIVE ACTION IS NOT INDICATED. SHOULD ADD'L SUBSTANTIVE INFO BE REC'D, THE COMPLAINT WILL BE REOPENED. ZIMMER, INC. CONSIDERS THE INVESTIGATION CLOSED.

Description of Event or Problem · 1

IT IS REPORTED THAT THE PT WAS REVISED FOR INSTABILITY. THE TIBIAL COMPONENT HAD DRIFTED INTO VARUS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 UNKNOWN ZIMMER TIBIAL BASEPLATE KNEE PROSTHESIS HSH ZIMMER INC.

Patients

Seq Age Sex Outcome Treatment
1 58 YR Required Intervention LOT #UNK| UNKNOWN ZIMMER ARTICULAR SURFACE, CATALOG #UNK,