FDA Adverse Event Injury Summary report: N

LEHEY CLAMP

MDR report key: 423936 · Received October 22, 2002

Report

Report Number
MW1026497
Event Type
Injury
Date Received
October 22, 2002
Date of Event
September 5, 2002
Report Date
October 14, 2002
Manufacturer
PILLING CO
Product Code
GDJ
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
AZ, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

TIP OF CLAMP BROKE OFF WHILE PULLING OUT TISSUE. METAL PIECE WAS REMOVED THROUGH THE REGULAR COURSE OF THE SURGERY. NO ADVERSE EFFECTS. DEVICE WAS SENT OUT OF SVC AND MARKED AS "BROKEN" BY NURSING STAFF. DEVICE IS NOT AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LEHEY CLAMP CLAMP GDJ PILLING CO 17-1155-353 T *

Patients

Seq Age Sex Outcome Treatment
1 * Required Intervention