FDA Adverse Event Malfunction Summary report: N

LEEP SYSTEM 1000 ESU GEN.

MDR report key: 6131879 · Received November 29, 2016

Report

Report Number
1216677-2016-00067
Event Type
Malfunction
Date Received
November 29, 2016
Date of Event
July 20, 2016
Report Date
November 10, 2016
Manufacturer
COOPERSURGICAL, INC.
Product Code
HGI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NH, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

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 (B)(4) PROJECT #(B)(4)- LEEP SYSTEM 1000 ROOT CAUSE. THIS CONCLUDES COOPERSURGICAL' S ROOT CAUSE INVESTIGATION. COOPERSURGICAL, INC. WILL CONTINUE TO MONITOR THE COMPLAINT CONDITION FOR TENDING AND SAFETY.

Description of Event or Problem · 1

REVIEW OF SERVICE AND REPAIR LOG REF REPAIR LOG NO.(B)(6). PER REPAIR AUTH FORM : "PLEASE TEST GENERATOR DOES NOT SEEM TO BE CUTTING CORRECTLY" "IS THIS A COMPLAINT ?: NO. WAS THERE PATIENT INJURY?: NO". (B)(4).

Description of Event or Problem · 1

REVIEW OF SERVICE AND REPAIR LOG REF REPAIR LOG NO. (B)(4) PER REPAIR AUTH FORM : "PLEASE TEST GENERATOR DOES NOT SEEM TO BE CUTTING CORRECTLY" "IS THIS A COMPLAINT : NO WAS THERE PATIENT INJURY: NO" (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
784831 LEEP SYSTEM 1000 ESU GEN. LEEP 1000 HGI COOPERSURGICAL, INC. 52969 N/A

Patients

Seq Age Sex Outcome Treatment
1 Other