FDA Adverse Event Malfunction Summary report: N

ATTUNE RP TIB BASE SZ 6 POR

MDR report key: 12422253 · Received September 3, 2021

Report

Report Number
1818910-2021-19311
Event Type
Malfunction
Date Received
September 3, 2021
Date of Event
March 11, 2021
Report Date
January 25, 2021
Manufacturer
DEPUY IRELAND - 9616671
Product Code
NJL
UDI-DI
10603295416289
PMA / PMN Number
P830055
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 0

PRODUCT COMPLAINT # ==> (B)(4) INVESTIGATION SUMMARY ==> NO DEVICE ASSOCIATED WITH THIS REPORT WAS RECEIVED FOR EXAMINATION. THE INFORMATION RECEIVED WILL BE RETAINED FOR POTENTIAL SERIES INVESTIGATIONS IF TRIGGERED BY TREND ANALYSIS, POST MARKET SURVEILLANCE, OR OTHER EVENTS WITHIN THE QUALITY SYSTEM. DEPUY CONSIDERS THE INVESTIGATION CLOSED. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE INFORMATION WILL BE REVIEWED AND THE INVESTIGATION WILL BE RE-OPENED AS NECESSARY. DEVICE HISTORY LOT ==> PRODUCT CODE (B)(4)WORK ORDER(B)(6) WAS MANUFACTURED ON 24-JUNE-2020. (B)(6) PARTS WERE MANUFACTURED PER SPECIFICATION AND ALL RAW MATERIALS MET SPECIFICATION. 2 SCRAP PARTS ASSOCIATED WITH THIS LOT. THE PARTS WERE SCRAPPED FOR REASON CODE A164 (PART THICKNESS) AT STAGE 1 LAP. ALL PARTS WERE INSPECTED AS PER (B)(6) REV 1 (TM ATTUNE CEMENTLESS RP TIBIAL BASES KEMET THICKNESS INSPECTION POST STAGE 1) WITH THE 2 PARTS FAILING BEING SCRAPPED. FURTHERMORE, AT THE AQUABLAST PROCESS STEP ALL PARTS ARE INSPECTED FOR THE PRESENCE OF RAISED POROCOAT OR DELAMINATION. AS PER 103071597 REV 3 (SWS ATTUNE CEMENTLESS RP TIB BASE AQUABLAST TRAYS VS) JEC 1 ¿PICKING IS ACCEPTABLE TO CONFIRM IF RAISED BEADS OR DELAMINATION PRESENT, FOLLOWED BY AQUABLAST ONLY. PICKING USED TO AID REMOVAL OF RAISED BEADS. TO VERIFY THE POROCOAT BEAD BOND INTEGRITY AFTER PICKING OF BEADS. (B)(6) ASSOCIATED WITH THIS LOT. 4 PARTS REPROCESSED FOR CLOUDS ON FACE THIS MRR HAS NO CORRELATION WITH THE COMPLAINT FAILURE MODE. NO NON-CONFORMANCE IS ASSOCIATED WITH THIS LOT.

Additional Manufacturer Narrative · 0

PRODUCT COMPLAINT # (B)(4). THIS REPORT IS BEING SUBMITTED PURSUANT TO THE PROVISIONS OF 21 CFR, PART 803. THIS REPORT MAY BE BASED ON INFORMATION WHICH HAS NOT BEEN INVESTIGATED OR VERIFIED PRIOR TO THE REQUIRED REPORTING DATE. THIS REPORT DOES NOT REFLECT A CONCLUSION BY DEPUY SYNTHES JOINT RECONSTRUCTION, OR ITS EMPLOYEES THAT THE REPORT CONSTITUTES AN ADMISSION THAT THE PRODUCT, DEPUY SYNTHES JOINT RECONSTRUCTION, OR ITS EMPLOYEES CAUSED OR CONTRIBUTED TO THE POTENTIAL EVENT DESCRIBED IN THIS REPORT. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL REPORT, A FOLLOW-UP REPORT WILL BE FILED AS APPROPRIATE.

Description of Event or Problem · 0

ADDITIONAL INFORMATION RECEIVED INDICATED THAT THE PATIENT WAS NOT REVISED. THE COMPONENTS WERE WELL-FIXED.

Additional Manufacturer Narrative · 1

PRODUCT COMPLAINT #: (B)(4). IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.

Description of Event or Problem · 1

COMPASS CASE REPORT (B)(4): THIS PATIENT HAD BILATERAL ATTUNE PRESSFIT KNEES. THE PATIENT HAD HER 6 WEEK FOLLOW UP, AND THE SURGEON NOTICED ON THE X-RAYS THAT BEADS FROM THE LEFT TIBIAL TRAY HAVE COME OFF. THIS HAS NOT HAD AN AFFECT ON THE PATIENT YET. THE "BEAD SHEDDING" THAT IS OBSERVED IS BECOMING A COMMON OCCURENCE WITH THIS PRODUCT. THIS SEEMS TO BE SEEN IN ABOUT 10% OF THESE PRODUCTS. IF ANYONE IS INTERESTED IN PICTURES, I CAN SEND THE IMAGES THAT THE SURGEON HAS SENT TO ME. NO SURGICAL DELAY. DOI: (B)(6) /2021.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1322014 ATTUNE RP TIB BASE SZ 6 POR ATTUNE CEMENTLESS IMPLANTS : KNEE TIBIAL TRAY NJL DEPUY IRELAND - 9616671 1506-11-006 9541709 10603295416289

Patients

Seq Age Sex Outcome Treatment
1