FDA Adverse Event Injury Summary report: N

VICRYL (POLYGLACTIN 910) SUTURE

MDR report key: 4220596 · Received November 3, 2014

Report

Report Number
2210968-2014-15195
Event Type
Injury
Date Received
November 3, 2014
Report Date
October 14, 2014
Manufacturer
ETHICON INC.
Product Code
GAM
PMA / PMN Number
K022269
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OR, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

(B)(4). 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 A SURGICAL EYE PROCEDURE ON AN UNKNOWN DATE AND SUTURE WAS USED. IT WAS NOTED DURING THE 2ND OR 3RD POST OP VISIT THAT THE PATIENT HAD DEVELOPED AN ABSCESS. THE ABSCESS WAS OPENED AND DRAINED. ANTIBIOTIC OINTMENT WAS PRESCRIBED. THE ABSCESS RESOLVED. ADDITIONAL INFORMATION HAS BEEN REQUESTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
702693 VICRYL (POLYGLACTIN 910) SUTURE SUTURE, ABSORBABLE, SYNTHETIC GAM ETHICON INC. UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention