FDA Adverse Event Malfunction Summary report: N

LEEP SYSTEM 1000 ESU GEN.

MDR report key: 5614259 · Received April 28, 2016

Report

Report Number
1216677-2016-00026
Event Type
Malfunction
Date Received
April 28, 2016
Date of Event
March 4, 2016
Report Date
November 9, 2016
Manufacturer
COOPERSURGICAL, INC.
Product Code
HGI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

COOPERSURGICAL INC. IS CURRENTLY INVESTIGATING THE REPORTED COMPLAINT CONDITION. THE DEVICE INVOLVED IN THE COMPLAINT WAS RETURNED BY THE CUSTOMER AND EVALUATED. ONCE THE INVESTIGATION IS COMPLETED A FOLLOW-UP REPORT WILL BE FILED. (B)(4).

Additional Manufacturer Narrative · 1

(B)(4). PLEASE FIND ATTACHED THE LEEP 1000 FINAL MDR SUBMISSION PACKAGE, REGARDING ALL INITIAL MDR'S, AND RETRO REVIEW INITIAL MDR'S FILED FOR REPORTS OF INTERMITTENT FUNCTION DURING USE. THE DOCUMENTS INCLUDED IN THIS PACKAGE ARE AS FOLLOWS: LEEP SYSTEM INVESTIGATION SUMMARY. LEEP 1000 TECH BULLETIN COVER LETTER. TECH SERVICE BULLETIN 12151. PROJECT #1676 - LEEP SYSTEM 1000 ROOT CAUSE THIS CONCLUDES COOPERSURGICAL' S ROOT CAUSE INVESTIGATION. COOPERSURGICAL, INC. WILL CONTINUE TO MONITOR THE COMPLAINT CONDITION FOR TRENDING AND SAFETY.

Description of Event or Problem · 1

REVIEW OF REPAIR ORDER LOG (B)(4). PER REPAIR AUTHORIZATION FORM: "WHEN FOOT PEDAL IS PRESSED, MACHINE WORKS ABOUT 3 SECONDS, THEN STOPS WORKING." (B)(4).

Description of Event or Problem · 1

(B)(4). PER REPAIR AUTHORIZATION FORM: "WHEN FOOT PEDAL IS PRESSED, MACHINE WORKS ABOUT 3 SECONDS, THEN STOPS WORKING." (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
272961 LEEP SYSTEM 1000 ESU GEN. LEEP SYSTEM 1000 ESU GEN. HGI COOPERSURGICAL, INC. 52969 N/A

Patients

Seq Age Sex Outcome Treatment
1 Other