FDA Adverse Event Malfunction Summary report: N

STRATAFIX KNOTLESS TISSUE CONTROL DEVICE

MDR report key: 4361035 · Received December 19, 2014

Report

Report Number
3008845715-2014-00080
Event Type
Malfunction
Date Received
December 19, 2014
Date of Event
December 4, 2014
Report Date
December 17, 2014
Manufacturer
SURGICAL SPECIALTIES PUERTO RICO INC.
Product Code
NEW
PMA / PMN Number
K051609
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

THE ACTUAL PRODUCT INVOLVED WITH THE INCIDENT REPORTED WILL NOT BE RETURNED. METHOD: THE ACTUAL PRODUCT INVOLVED WITH THE INCIDENT REPORTED WILL NOT BE RETURNED. NO PRODUCT EVALUATION CAN BE PERFORMED. NO INVENTORY AVAILABLE FOR THE LOT REPORTED. RELEVANT PORTIONS OF THE DEVICE HISTORY RECORD WERE REVIEWED. FINISHED GOOD PRODUCT WAS RECEIVED INTO INVENTORY WITHOUT QUALITY ISSUES. THE PRODUCT FROM THIS FINISHED GOOD LOT AND ALL OF THE COMPONENTS MET SURGICAL SPECIALTIES PUERTO RICO INC. REQUIREMENTS THROUGHOUT THE INCOMING, MANUFACTURING AND THE FINAL INSPECTION PROCESSES. NEEDLE SUPPLIER, WHICH IS OUR CUSTOMER AS WELL, WAS CONTACTED TO VERIFY IF THERE WERE ANY QUALITY ISSUES RELATED TO THE NEEDLE BATCHES USED IN THE MANUFACTURING OF THE LOTS REVIEWED. AS OF THE DAY OF THIS REPORT, INFORMATION HAS NOT BEEN RECEIVED FROM SUPPLIER. THE NEEDLE SUPPLIER HAS BEEN MADE AWARE OF THIS COMPLAINT FOR A CONTINUED INVESTIGATION. REFERENCE: (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED THAT, DURING A TOTAL HIP REPLACEMENT, THE TIP OF THE NEEDLE BROKE OFF DURING THE PROCEDURE. THE NEEDLE WAS SUCCESSFULLY RETRIEVED FROM THE PATIENT. (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
837712 STRATAFIX KNOTLESS TISSUE CONTROL DEVICE BARBED MATERIAL/NEEDLES NEW SURGICAL SPECIALTIES PUERTO RICO INC. SXPD2B40505 MCMG620

Patients

Seq Age Sex Outcome Treatment
1 NA NONE MADE AVAILABLE