FDA Adverse Event Injury Summary report: N

PDS LL PLUS ANTIBACTERIAL SUTURE

MDR report key: 3003943 · Received March 14, 2013

Report

Report Number
2210968-2013-02460
Event Type
Injury
Date Received
March 14, 2013
Date of Event
February 14, 2013
Report Date
February 21, 2013
Manufacturer
ETHICON, INC.
Product Code
NEW
PMA / PMN Number
K061037
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). IT WAS REPORTED THAT A PATIENT UNDERWENT AN OPEN ABDOMINAL SURGERY FOR ACUTE INTESTINAL ISCHEMIA ON (B)(6) 2013 AND SUTURE WAS USED FOR ABDOMINAL CLOSURE. THE PATIENT EXPERIENCED A WOUND DEHISCENCE ON (B)(6) 2013. A RE-OPERATION WAS PERFORMED AT THAT TIME. THE WOUND WAS RECLOSED WITH A DIFFERENT SUTURE. THE WOUND WAS ALSO TREATED WITH WOUND VACUUM THERAPY. THE SURGEON OPINES THAT THE WOUND DEHISCED DUE TO THE PATIENT'S OBESITY AND A SECONDARY DIAGNOSIS OF DIABETES. (B)(4). CONCLUSION: REPRESENTATIVE SAMPLES WERE RETURNED FOR EVALUATION. THEY WERE VISUALLY AND FUNCTIONALLY EXAMINED FOR TENSILE STRENGTH AND THEY MET THE REQUIREMENTS. IN ADDITION, A REVIEW OF THE BATCH MANUFACTURING RECORDS WAS CONDUCTED AND THE BATCH MET ALL FINISHED GOODS RELEASE CRITERIA.

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.

Description of Event or Problem · 1

IT WAS REPORTED THAT A PATIENT UNDERWENT AN UNKNOWN PROCEDURE ON AN UNKNOWN DATE AND SUTURE WAS USED FOR ABDOMINAL CLOSURE. THE PATIENT EXPERIENCED WOUND DEHISCENCE. ADDITIONAL INFORMATION HAS BEEN REQUESTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
106985 PDS LL PLUS ANTIBACTERIAL SUTURE SUTURE, ABSORBABLE NEW ETHICON, INC. NA ELM635

Patients

Seq Age Sex Outcome Treatment
1 57 YR Required Intervention