FDA Adverse Event Malfunction Summary report: N

CB030, 5MMX35CM EPIX LAPA SCISSOR, 10/BX

MDR report key: 11638601 · Received April 8, 2021

Report

Report Number
2027111-2021-00436
Event Type
Malfunction
Date Received
April 8, 2021
Date of Event
April 1, 2021
Report Date
June 9, 2021
Manufacturer
APPLIED MEDICAL RESOURCES
Product Code
HET
UDI-DI
00607915110123
PMA / PMN Number
K062169
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
BE
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 0

THE EVENT UNIT WAS RETURNED TO APPLIED MEDICAL FOR EVALUATION. TESTING WAS PERFORMED ON THE EVENT UNIT, WHICH CONFIRMED THAT THE RETURNED UNIT WAS UNABLE TO CUT CONSISTENTLY ACROSS THE ENTIRE LENGTH OF THE BLADE. ENGINEERING OBSERVED A SMALL GAP BETWEEN THE TIPS OF THE BLADES. BASED ON THE CONDITION OF THE EVENT UNIT AND DESCRIPTION OF THE EVENT, THE SCISSORS WERE UNABLE TO CUT DUE TO THE GAP THAT WERE OBSERVED BETWEEN THE TIPS OF THE BLADES ON THE RETURNED UNIT. HOWEVER, THE EXACT ROOT CAUSE OF THE GAP COULD NOT BE DETERMINED BASED ON THE EVALUATION OF THE RETURNED UNIT. APPLIED MEDICAL CONTINUOUSLY SEEKS TO IMPROVE THE FORM, FUNCTION, AND EASE OF USE OF ITS PRODUCTS. AS PART OF THIS PROCESS, APPLIED MEDICAL IS CURRENTLY RESEARCHING POSSIBLE ENHANCEMENTS INTENDED TO FURTHER MINIMIZE THE POTENTIAL FOR THIS TYPE OF EVENT TO OCCUR.

Description of Event or Problem · 0

PROCEDURE PERFORMED: LAPAROSCOPIC VAGINAL HYSTERECTOMY. SCISSORS NOT SHARP. ADDITIONAL INFORMATION RECEIVED FROM APPLIED MEDICAL REPRESENTATIVE VIA EMAIL ON 06-APR-2021: THE SCISSORS DIDN'T CUT FROM THE BEGINNING OF THE PROCEDURE. THEY TOOK ANOTHER. INTERVENTION: CHANGE OF DEVICE. PATIENT STATUS: OKE.

Additional Manufacturer Narrative · 1

THE INCIDENT DEVICE IS ANTICIPATED TO RETURN. A FOLLOW-UP REPORT WILL BE PROVIDED UPON COMPLETION OF INVESTIGATION.

Description of Event or Problem · 1

PROCEDURE PERFORMED: LAPAROSCOPIC VAGINAL HYSTERECTOMY. SCISSORS NOT SHARP. ADDITIONAL INFORMATION RECEIVED FROM APPLIED MEDICAL REPRESENTATIVE VIA EMAIL ON 06-APR-2021: THE SCISSORS DIDN'T CUT FROM THE BEGINNING OF THE PROCEDURE. THEY TOOK ANOTHER. INTERVENTION: CHANGE OF DEVICE. PATIENT STATUS: OKE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
531156 CB030, 5MMX35CM EPIX LAPA SCISSOR, 10/BX LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES) HET APPLIED MEDICAL RESOURCES CB030 1399251 00607915110123

Patients

Seq Age Sex Outcome Treatment
1