FDA Adverse Event Malfunction Summary report: N

LEEP SYSTEM 1000 ESU.GEN.

MDR report key: 5614234 · Received April 28, 2016

Report

Report Number
1216677-2016-00012
Event Type
Malfunction
Date Received
April 28, 2016
Date of Event
January 28, 2016
Report Date
November 9, 2016
Manufacturer
COOPERSURGICAL, INC.
Product Code
HGI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, 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 HAS BEEN RETURNED BY THE CUSTOMER AND EVALUATED. ONCE THE INVESTIGATION PROCESS IS COMPLETED A FOLLOW-UP REPORT WILL BE FILED. REFERENCE E-COMPLAINT: (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 #(B)(4) - 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 SERVICE AND REPAIR LOGS. REFERENCE REPAIR ORDER LOG (B)(4), REPAIR AUTHORIZATION FORM. "DRAGGING OF LOOP, LEAVES JAGGES EDGES/BLEEDING." REF E-COMPLAINT: (B)(4).

Description of Event or Problem · 1

REVIEW OF SERVICE AND REPAIR LOGS. REFERENCE REPAIR ORDER LOG (B)(4) - REPAIR AUTHORIZATION FORM. "DRAGGING OF LOOP, LEAVES JAGGED EDGES/BLEEDING." (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
272880 LEEP SYSTEM 1000 ESU.GEN. LEEP SYSTEM 1000 HGI COOPERSURGICAL, INC. 52969 N/A

Patients

Seq Age Sex Outcome Treatment
1 Other