FDA Adverse Event Malfunction Summary report: N

TPRLC 133 MP TYPE1 PPS SO 17.0

MDR report key: 9702159 · Received February 12, 2020

Report

Report Number
0001825034-2020-00684
Event Type
Malfunction
Date Received
February 12, 2020
Date of Event
January 29, 2020
Report Date
June 16, 2020
Manufacturer
ZIMMER BIOMET, INC.
Product Code
KWZ
PMA / PMN Number
K110400
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

THIS FOLLOW-UP REPORT IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. COMPLAINT SAMPLE WAS EVALUATED AND THE REPORTED EVENT WAS CONFIRMED. INSPECTION OF THE RETURNED DEVICE REVEALED THERE WAS DEBRIS INSIDE THE STERILE PACKAGING THAT IS CONSISTENT WITH THE APPEARANCE OF FOAM DEBRIS FROM THE FOAM PACKAGING INSIDE THE STERILE BARRIER AND BLACK DEBRIS CONSISTENT WITH POROUS MATERIAL FROM THE DEVICE. DEVICE HISTORY RECORD (DHR) WAS REVIEWED AND NO DISCREPANCIES WERE FOUND. THESE PRODUCTS WERE LIKELY CONFORMING WHEN THEY LEFT ZIMMER BIOMET CONTROL. THE ROOT CAUSE OF THE REPORTED ISSUE IS ATTRIBUTED TO TRANSIT DAMAGE CAUSING THE FOAM PACKAGING AND POROUS MATERIAL FROM DEVICE TO BECOME ABRADED AND SHED. 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 · 0

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

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT MEDICAL PRODUCTS: TPRLC 133 T1 PPS HO 16X152MM, CAT# 51-104160, LOT# 6047712. TPRLC 133 T1 PPS HO 9X137MM, CAT# 51-104090, LOT# 6057369. TPRLC XR MP T1 PPS 14X113MM, CAT# 51-145140, LOT# 3545229. TPRLC XR MP T1 PPS 14X113MM, CAT# 51-145140, LOT# 2884150. TPRLC XR MP T1 PPS 17X119MM, CAT# 51-145170, LOT# 3730608 . TPRLC 133 MP TYPE1 PPS SO 17.0, CAT# 51-106170, LOT# 3669984. TPRLC XR MP T1 PPS 16X117MM, CAT# 51-145160, LOT# 3029799. FOREIGN SOURCE: (B)(6). MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034-2020-00679, 0001825034-2020-00680, 0001825034-2020-00681, 0001825034-2020-00682, 0001825034-2020-00683, 0001825034-2020-00685, 0001825034-2020-00686.

Description of Event or Problem · 1

IT WAS REPORTED THAT DEBRIS WAS FOUND IN STERILE PACKAGING WHILE INVESTIGATING STOCK. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
165069 TPRLC 133 MP TYPE1 PPS SO 17.0 PROSTHESIS, HIP KWZ ZIMMER BIOMET, INC. NI 3564680

Patients

Seq Age Sex Outcome Treatment
1 SEE H10