FDA Adverse Event Injury Summary report: N

BMT 360 TIB AUG 71X10MM

MDR report key: 14986806 · Received July 12, 2022

Report

Report Number
0001825034-2022-01592
Event Type
Injury
Date Received
July 12, 2022
Date of Event
June 16, 2022
Report Date
November 10, 2022
Manufacturer
ZIMMER BIOMET, INC.
Product Code
JWH
UDI-DI
00880304481688
PMA / PMN Number
K093293
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AS
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

(B)(4). MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034-2022-01593, 0001825034-2022-01594, 0001825034-2022-01595, 0001825034-2022-01596, 0001825034-2022-01597, AND 0001825034-2022-01598. MEDICAL DEVICES: BMT 360 TIB AUG 67X10MM CATALOG#: 185232 LOT#: 622080. BMT 360 TIB LG CRUCIATE WING CATALOG#: 185651 LOT#: 160950. BMT SPLINED KNEE STM V2 18X80 CATALOG#: 148308 LOT#: 710510. BMT 360 TIB TRAY 67MM CATALOG#: 185202 LOT#: 718090. VNGD SSK PS TIB BRG 18X63/67 CATALOG#: 185068 LOT#: 845430. VANGUARD CR ILOK FEM-RT 62.5 CATALOG#: 183006 LOT#: 846430. FOREIGN SOURCE: AUSTRALIA. CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT 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.

Additional Manufacturer Narrative · 0

THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DEVICE HISTORY RECORD WAS REVIEWED AND NO DISCREPANCIES RELEVANT TO THE REPORTED EVENT WERE FOUND. ROOT CAUSE WAS UNABLE TO BE DETERMINED AS THE NECESSARY INFORMATION TO ADEQUATELY INVESTIGATE THE REPORTED EVENT WAS NOT PROVIDED. ROOT CAUSE WAS UNABLE TO BE DETERMINED AS THE NECESSARY INFORMATION TO ADEQUATELY INVESTIGATE THE REPORTED EVENT WAS NOT PROVIDED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS.

Additional Manufacturer Narrative · 0

THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034-2022-01592, 0001825034-2022-01593, 0001825034-2022-01594, 0001825034-2022-01595, 0001825034-2022-01596, 0001825034-2022-01597, 0001825034-2022-01598, 0001825034-2022-01917, 0001825034-2022-01918, AND 0001825034-2022-01919. D10 MEDICAL DEVICES: BMT 360 TIB AUG 71X10MM, CATALOG#: 185233, LOT#: 956120. BMT 360 TIB LG CRUCIATE WING, CATALOG#: 185651, LOT#: 805380. BMT SPLINED KNEE STM V2 18X40, CATALOG#: 148293, LOT#: 998960. BMT 360 TIB TRAY 71MM, CATALOG#: 185203, LOT#: 502940. VNGD SSK PSC TIB BRG 14X71/75, CATALOG#: 183884, LOT#: 820100. VNGD SSK 360 FEMUR L 67.5, CATALOG#: 185285, LOT#: 6668552. BMT 360 2.5MM OFFSET ADAPTER, CATALOG#: 185210, LOT#: 136930. BMT SPLINED KNEE STM V2 18X40, CATALOG#: 148293, LOT#: 998960. BMT 360 2.5MM OFFSET ADAPTER, CATALOG#: 185210, LOT#: 057070. SERIES A PAT THN 34 3 PEG, CATALOG#: 184786, LOT#: 512610.

Description of Event or Problem · 0

IT WAS REPORTED THE PATIENT UNDERWENT A RIGHT KNEE REVISION APPROXIMATELY TWENTY-TWO MONTHS POST IMPLANTATION DUE TO PAIN.

Description of Event or Problem · 0

NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.

Description of Event or Problem · 0

IT WAS REPORTED THE PATIENT UNDERWENT A LEFT KNEE REVISION APPROXIMATELY TWENTY-TWO MONTHS POST IMPLANTATION DUE TO PAIN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
721864 BMT 360 TIB AUG 71X10MM PROSTHESIS, KNEE JWH ZIMMER BIOMET, INC. N/A 970810 00880304481688

Patients

Seq Age Sex Outcome Treatment
1 Unknown Hospitalization| R SEE H10| SEE H10