FDA Adverse Event Malfunction Summary report: N

COATED VICRYL PLUS ANTIBACTERIAL (POLYGLACTIN 910)

MDR report key: 2833595 · Received November 15, 2012

Report

Report Number
2210968-2012-07327
Event Type
Malfunction
Date Received
November 15, 2012
Date of Event
April 24, 2012
Report Date
October 23, 2012
Manufacturer
ETHICON, INC.
Product Code
GAM
PMA / PMN Number
K032420
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SP
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

THIS MEDWATCH REPORT IS BEING VOIDED AS IT IS A DUPLICATE OF MEDWATCH REPORT # 2210968-2012-02108. PLEASE SEE MEDWATCH REPORT # 2210968-2012-02108 FOR ALL INFORMATION REGARDING THIS EVENT.

Additional Manufacturer Narrative · 1

(B)(4): IT WAS REPORTED THAT THE PROCEDURE WAS PERFORMED ON EITHER (B)(4) 2012 AND THE NEEDLE BROKE BECAUSE IT WAS MUCH TOO SMALL TO CLOSE THE UTERUS BY LAPAROSCOPY. WHEN A LARGER NEEDLE WAS USED, THERE WERE NO FURTHER PROBLEMS.

Additional Manufacturer Narrative · 1

(B)(4). CONCLUSION: NO CONCLUSION CAN BE DRAWN AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE OBTAINED, A SUPPLEMENTAL 3500A FORM WILL BE SUBMITTED ACCORDINGLY.

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT UNDERWENT AN UNKNOWN PROCEDURE ON (B)(6) 2012 AND SUTURE WAS USED. DURING THE PROCEDURE THE NEEDLE BROKE. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. ADDITIONAL INFORMATION HAS BEEN REQUESTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 COATED VICRYL PLUS ANTIBACTERIAL (POLYGLACTIN 910) SUTURE, ABSORBABLE GAM ETHICON, INC. NA NI

Patients

Seq Age Sex Outcome Treatment
1