FDA Adverse Event Malfunction Summary report: Y

DUAL TRIGGER PIN COLLET

MDR report key: 8284748 · Received January 29, 2019

Report

Report Number
0001811755-2019-00270
Event Type
Malfunction
Date Received
January 29, 2019
Date of Event
December 25, 2018
Report Date
July 29, 2019
Manufacturer
STRYKER INSTRUMENTS-KALAMAZOO
Product Code
HWE
UDI-DI
07613327304558
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

THIS RECORD IS A CONSOLIDATION OF RECORDS SUMMARIZED AS A PART OF THE FDA VOLUNTARY MALFUNCTION SUMMARY REPORTING PROGRAM. SUPPLEMENTAL RATIONALE CORRECTED DATA: 4 EVENTS WERE PREVIOUSLY REPORTED DURING THE REPORTING PERIOD; HOWEVER, - 4 PREVIOUSLY REPORTED EVENTS IN THIS REPORT SHOULD HAVE BEEN INCLUDED UNDER MFR REPORT # 0001811755-2019-00269. - 0 PREVIOUSLY REPORTED EVENTS ARE INCLUDED IN THIS FOLLOW-UP RECORD.

Description of Event or Problem · 0

THIS REPORT SUMMARIZES <NOE> 0 </NOE> MALFUNCTION EVENTS IN WHICH THE DEVICE WAS SHEDDING METAL DEBRIS.

Additional Manufacturer Narrative · 1

THIS RECORD IS A CONSOLIDATION OF RECORDS SUMMARIZED AS A PART OF THE FDA VOLUNTARY MALFUNCTION SUMMARY REPORTING PROGRAM. REPORTED EVENTS: 4 EVENTS WERE REPORTED FOR THIS QUARTER. PRODUCT RETURN STATUS: 4 DEVICES WERE RECEIVED. EVALUATION STATUS: 4 REPORTED EVENTS WERE NOT CONFIRMED DURING TESTING. ADDITIONAL INFORMATION: 4 DEVICES WERE NOT LABELED FOR SINGLE-USE, 4 DEVICES WERE NOT REPROCESSED AND REUSED.

Description of Event or Problem · 1

THIS REPORT SUMMARIZES 4 MALFUNCTION EVENTS IN WHICH THE DEVICE WAS SHEDDING METAL DEBRIS, 4 EVENTS HAD NO PATIENT INVOLVEMENT; NO PATIENT IMPACT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
79858 DUAL TRIGGER PIN COLLET INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT HWE STRYKER INSTRUMENTS-KALAMAZOO 07613327304558

Patients

Seq Age Sex Outcome Treatment
1