FDA Adverse Event Malfunction Summary report: N

COATED VICRYL PLUS (POLYGLACTIN 910) SUTURE

MDR report key: 1851269 · Received September 23, 2010

Report

Report Number
2210968-2010-01175
Event Type
Malfunction
Date Received
September 23, 2010
Date of Event
March 7, 2010
Report Date
August 24, 2010
Manufacturer
ETHICON, INC.
Product Code
GAM
PMA / PMN Number
K032420
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). RESULT: TWO REPRESENTATIVE SAMPLES WERE RETURNED FOR EVAL. THEY WERE VISUALLY AND FUNCTIONALLY EXAMINED FOR KNOT TENSILE STRENGTH AND THEY MET THE REQUIREMENTS. CONCLUSION: THE DEVICES WERE RECEIVED IN A CONDITION THAT MEETS SPECIFICATION. IN ADDITION, A REVIEW OF THE BATCH MANUFACTURING RECORDS WAS CONDUCTED AND THE BATCH MET ALL FINISHED GOODS RELEASE CRITERIA. THIS IS ONE OF SEVEN MEDWATCHES SUBMITTED FOR THE SAME PT. SEE ALSO MEDWATCH 2210968-2010-01170, 2210968-2010-01171, 2210968-2010-01172, 2210968-2010-01173, 2210968-2010-01174, AND 2210968-2010-01176.

Description of Event or Problem · 1

IT WAS REPORTED THAT A PT UNDERWENT AN ANTEBRACHIUM FLAP LENGTHENING PROCEDURE ON (B)(6) 2010 AND SUTURE WAS USED TO SEW "REAL LEATHER" DISCONTINUOUSLY. TWO DAYS AFTER THE PROCEDURE, THE SURGEON FOUND THE SUTURE WAS BROKEN. NOW THE PT'S WOUND HAS HEALED UP.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 COATED VICRYL PLUS (POLYGLACTIN 910) SUTURE SUTURE, ABSORBABLE GAM ETHICON, INC. NA BM2257

Patients

Seq Age Sex Outcome Treatment
1 10 YR