FDA Adverse Event Injury Summary report: N

PALACOS

MDR report key: 7278334 · Received February 16, 2018

Report

Report Number
0001822565-2018-00965
Event Type
Injury
Date Received
February 16, 2018
Date of Event
February 24, 2017
Report Date
March 19, 2018
Manufacturer
ZIMMER BIOMET, INC.
Product Code
LOD
PMA / PMN Number
PK142157
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MS, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT. PLEASE ALSO SEE ASSOCIATED REPORT(S): 0001822565 - 2018 - 00966. THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED. NOT RETURNED TO MANUFACTURER.

Additional Manufacturer Narrative · 1

CONCOMITANT MEDICAL PRODUCTS: ECHO FX 7MM STD FEMORAL CAT: 12-151307 LOT: 697250, 28MM MOD HD STD NECK TP1 TAPER CAT: 163662 LOT: 326480, RINGLOC BI-POLAR 28X46MM CAT: 11-165216 LOT: 444440, INGL ANSR IMPCT DSTL PSTNR 10 CAT: 162640 LOT: 786980. REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DEVICE HISTORY RECORD WAS REVIEWED AND NO DISCREPANCIES WERE FOUND. 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.

Description of Event or Problem · 1

IT WAS REPORTED THE PATIENT WAS REVISED DUE TO INFECTION. THERE WERE NO COMPLICATIONS OR DELAYS REPORTED. NO FURTHER INFORMATION HAS BEEN MADE AVAILABLE AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
119352 PALACOS BONE CEMENT LOD ZIMMER BIOMET, INC. N/A 81494445

Patients

Seq Age Sex Outcome Treatment
1 65 YR Hospitalization| R