FDA Adverse Event Injury Summary report: N

UNKNOWN ZIMMER METAPHYSEAL-DIAPHYSEAL NAIL

MDR report key: 6737197 · Received July 24, 2017

Report

Report Number
0001822565-2017-05132
Event Type
Injury
Date Received
July 24, 2017
Report Date
July 24, 2017
Manufacturer
ZIMMER, INC.
Product Code
JDS
PMA / PMN Number
PNI
Removal / Correction Number
N/A
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
KS
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). HAYOUNG KIM, SANG KI LEE, KAP JUNG KIM, JAE HOON AHN, WON SIK CHOY, YONG IN KIM, AND JEA YUN KOO ¿TIBIAL LENGTHENING USING A REAMED TYPE INTRAMEDULLARY NAIL AND AN ILIZAROV EXTERNAL FIXATOR¿. INTERNATIONAL ORTHOPAEDICS (SICOT) (2009) 33:835-841 THE COMPLAINT DEVICE IS NOT EXPECTED FOR RETURN CURRENTLY, BUT A SUPPLEMENTAL MEDWATCH 3500A WILL BE SUBMITTED UPON RECEIPT OF ADDITIONAL INFORMATION. THE REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. A DEVICE HISTORY RECORD REVIEW WAS UNABLE TO BE PERFORMED AS THE LOT NUMBER OF THE DEVICE INVOLVED IN THE EVENT IS UNKNOWN. A COMPLAINT HISTORY REVIEW WAS UNABLE TO BE PERFORMED AS THE PART AND LOT NUMBERS ARE UNKNOWN. A ROOT CAUSE WAS UNABLE TO BE DETERMINED AS THE NECESSARY INFORMATION TO ADEQUATELY INVESTIGATE THE REPORTED EVENT WAS NOT PROVIDED.

Description of Event or Problem · 1

IT WAS REPORTED IN A JOURNAL ARTICLE THAT ONE (1) PATIENT WHO UNDERWENT A TIBIAL LENGTHENING PROCEDURE UTILIZING AN INTRAMEDULLARY NAIL AND EXTERNAL FIXATOR, EXPERIENCED ANKLE JOINT EQUINUS CONTRACTURE, AND UNDERWENT AN ACHILLES TENDON LENGTHENING AND POSTERIOR CAPSULOTOMY AT 6 MONTHS POSTOPERATIVELY BECAUSE THE COMPLICATION DID NOT RESPOND TO CLOSED TREATMENT. NO FURTHER INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
517310 UNKNOWN ZIMMER METAPHYSEAL-DIAPHYSEAL NAIL FIXATION, NAIL JDS ZIMMER, INC. N/A NI

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R