FDA Adverse Event Injury Summary report: N

TIBIAL INSERT 14MM -L-

MDR report key: 6595376 · Received May 26, 2017

Report

Report Number
0009610576-2017-00021
Event Type
Injury
Date Received
May 26, 2017
Report Date
May 26, 2017
Manufacturer
BIOMET SPAIN, S.L.
Product Code
JWH
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
SP
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT PRODUCTS¿ STRAIGHT STEM 13X80MM CATALOG 1528-30 LOT 03044950; SCREW CATALOG 1521-16 LOT 03094566; FEMUR 64MM CATALOG 1521-11 LOT 00090747; TIBIA 72MM LEFT CATALOG 1521-05 LOT 04045827; TIBIAL PIN 1520-34 LOT 04017480; CLIP CATALOG 1520-22 LOT 05057876; STRAIGHT STEM 11.5X210MM CATALOG 1528-12 LOT 02072635. (B)(4). THIS PRODUCT IS NOT CLEARED OR DISTRIBUTED IN THE U.S. HOWEVER, THIS REPORT IS BEING SUBMITTED AS ZIMMER BIOMET MANUFACTURES A SIMILAR DEVICE THAT IS CLEARED OR DISTRIBUTED IN THE UNITED STATES UNDER 510(K) NUMBER K945028. CUSTOMER HAS NOT INDICATED THAT THE PRODUCT WILL BE RETURNED TO ZIMMER BIOMET FOR INVESTIGATION. THE INVESTIGATION IS IN PROCESS. 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: 0009610576-2017-00017, 0009610576-2017-00018, 0009610576-2017-00019, 0009610576-2017-00020, 0009610576-2017-00022, 0009610576-2017-00023, AND 0009610576-2017-00024.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT HAS BEEN INDICATED FOR A KNEE REVISION DUE TO UNKNOWN REASONS. NO REVISION HAS BEEN REPORTED TO DATE. ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
375550 TIBIAL INSERT 14MM -L- PROSTHESIS, KNEE JWH BIOMET SPAIN, S.L. 2005061391

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention