FDA Adverse Event Injury Summary report: N

PROLENE POLYPROPYLENE SUTURE

MDR report key: 2860715 · Received December 6, 2012

Report

Report Number
2210968-2012-07937
Event Type
Injury
Date Received
December 6, 2012
Report Date
November 16, 2012
Manufacturer
ETHICON, INC.
Product Code
GAW
PMA / PMN Number
N16374
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). CONCLUSION: THE PRODUCT UPON WHICH THIS MEDWATCH IS BASED IS ANTICIPATED. ONCE THE PRODUCT IS RECEIVED, ANY FURTHER INFORMATION DERIVED FROM THE EVALUATION WILL BE SUBMITTED IN A SUPPLEMENTAL 3500A FORM. ADDITIONAL INFORMATION: - THE ACTUAL DEVICE BATCH NUMBER ASSOCIATED WITH THIS EVENT IS NOT KNOWN. THE INTERNATIONAL AFFILIATE REPORTS THE FOLLOWING POSSIBLE BATCH NUMBERS: BATCH ECB769 MFG DATE: 03/01/2012, EXP DATE: 01/31/2017. BATCH EDP116 MFG DATE: 04/01/2012, EXP DATE: 01/31/2017. IN ADDITION, A REVIEW OF THE BATCH MANUFACTURING RECORDS FOR THE POSSIBLE BATCH NUMBERS WAS CONDUCTED AND THE BATCHES MET ALL FINISHED GOODS RELEASE CRITERIA. THIS IS ONE OF FOUR MEDWATCHES BEING SUBMITTED. SEE ALSO MEDWATCH 2210968-2012-07935, 2210968-2012-07936, AND 2210968-2012-07938. THE SAME PATIENT IS REPRESENTED IN EACH MEDWATCH.

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT UNDERWENT A RE-OPERATION DUE TO DEHISCENCE OF THE FEMORAL ARTERY FOLLOWING A STENT PLACEMENT ON AN UNKNOWN DATE AND SUTURE WAS USED. THE PATIENT EXPERIENCED BLEEDING FROM THE ARTERY AGAIN AND REQUIRED ANOTHER SURGERY ON (B)(6) 2012. A NEW DEVICE WAS USED TO REPAIR THE VESSEL. THE PATIENT WAS ALSO GIVEN CRYSTAL VIOLET TO PREVENT MRSA. ADDITIONAL INFORMATION HAS BEEN REQUESTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PROLENE POLYPROPYLENE SUTURE SUTURE, NON-ABSORBABLE GAW ETHICON, INC. NA NI

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention