FDA Adverse Event Injury Summary report: N

ON-X MITRAL HEART VALVE - 27/29

MDR report key: 5995389 · Received October 3, 2016

Report

Report Number
1649833-2016-00031
Event Type
Injury
Date Received
October 3, 2016
Date of Event
December 9, 2014
Report Date
October 3, 2016
Manufacturer
ON-X LIFE TECHNOLOGIES, INC
Product Code
LWQ
UDI-DI
00851788001280
PMA / PMN Number
P000037
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

IN 2016, ON-X TECHNOLOGIES INCORPORATED (ON-X) BECAME A WHOLLY OWNED SUBSIDIARY OF CRYOLIFE, INC. (CRYOLIFE). A RETROSPECTIVE REVIEW OF THE ON-X COMPLAINT SYSTEM WAS PERFORMED TO IDENTIFY ANY AREAS REQUIRING ADDITIONAL ACTION AND TO APPROPRIATELY ASSIMILATE THE ON-X PROCESS INTO THE CRYOLIFE QUALITY MANAGEMENT SYSTEM. IN AN ABUNDANCE OF CAUTION THIS MDR IS BEING REPORTED TO SATISFY REGULATORY REPORTING OBLIGATIONS. THE ON-X 614 HEART VALVE DESIGN FMEA 940816 01 REV S THOROUGHLY IDENTIFIES THE PROCESS AND PRODUCT HAZARDS FOR APPROVED INDICATIONS. EACH INDIVIDUAL HAZARD IS MITIGATED AND REDUCED AS LOW AS POSSIBLE BY DESIGN AND PROCESS. POST PRODUCTION RESIDUAL RISK IS COMMUNICATED IN THE PRODUCT'S LABELING AND INSTRUCTION FOR USE (IFU). REOPERATION IS A KNOWN COMPLICATION OF PROSTHETIC VALVE IMPLANTATION AND IS LISTED IN THE IFU. WITHOUT RETURN OF THE VALVE, A SPECIFIC RISK CANNOT BE IDENTIFIED.

Description of Event or Problem · 1

IMPLANT RECOVERY CARD RECEIVED INDICATE THAT PATIENT RECEIVED ONXM 27/29 ON (B)(6) 2014 WHICH REQUIRED INTERVENTION/EXPLANT ON (B)(6) 2014 AND REPLACEMENT WITH AN ONXM-25 FOR UNSPECIFIED REASON. MULTIPLE ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION WERE MADE WITHOUT SUCCESS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
645722 ON-X MITRAL HEART VALVE - 27/29 MECHANICAL HEART VALVE LWQ ON-X LIFE TECHNOLOGIES, INC ONXM - 27/29 00851788001280

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| O