FDA Adverse Event Injury Summary report: N

STR MOD ACET INSERTER HANDLE

MDR report key: 6580866 · Received May 21, 2017

Report

Report Number
0001825034-2017-03394
Event Type
Injury
Date Received
May 21, 2017
Date of Event
April 25, 2017
Report Date
June 1, 2018
Manufacturer
BIOMET ORTHOPEDICS
Product Code
MDM
PMA / PMN Number
PEXEMPT
Removal / Correction Number
N/A
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

UPON REASSESSMENT OF THE REPORTED EVENT, IT WAS DETERMINED TO BE NOT REPORTABLE. THE INITIAL REPORT WAS FORWARDED IN ERROR AND SHOULD BE VOIDED.

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT PRODUCT(S): S313142 ZB120201 STR INSERTER 1/4-28 THRD KIT. S313141 119882 STR MOD ACET INSERTER HANDLE. A 14-103648 485440 UNIV 2-HOLE SHL 48MM LNR SZ 22. REPORT SOURCE: COUNTRY: (B)(6). CUSTOMER HAS INDICATED THAT THE PRODUCT IS IN PROCESS OF BEING RETURNED TO ZIMMER BIOMET FOR INVESTIGATION. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034 - 2017 - 03393.

Description of Event or Problem · 1

IT WAS REPORTED THAT PATIENT UNDERWENT LEFT THA DUE TO HIP OSTEOARTHRITIS. DURING IMPLANTATION OF THE CUP, THE HANDLE FRACTURED, THE THREAD FRACTURE COULDN¿T BE RETRIEVED FROM THE CUP. IN ORDER TO COMPLETE THE SURGERY, THE SURGEON THEN REMOVED THE CUP AND REPLACED IT. A 20 MINUTE DELAY WAS CAUSED. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
361975 STR MOD ACET INSERTER HANDLE PROSTHESIS, HIP MDM BIOMET ORTHOPEDICS N/A 119882

Patients

Seq Age Sex Outcome Treatment
1 65 YR Other