FDA Adverse Event Malfunction Summary report: N

SLIDING LOCK ATRAUMATIC GRASPER

MDR report key: 2110366 · Received April 25, 2011

Report

Report Number
2936485-2011-00244
Event Type
Malfunction
Date Received
April 25, 2011
Date of Event
March 28, 2011
Report Date
March 28, 2011
Manufacturer
STRYKER ENDOSCOPY SAN JOSE
Product Code
HRX
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
VA, US
Reporter Occupation
NOT APPLICABLE

Narratives

Additional Manufacturer Narrative · 1

ADDITIONAL INFORMATION WILL BE PROVIDED ONCE THE INVESTIGATION IS COMPLETED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE INSULATION WAS COMING OFF AT THE TIP OF THE PRODUCT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SLIDING LOCK ATRAUMATIC GRASPER GRASPER HRX STRYKER ENDOSCOPY SAN JOSE 0941550

Patients

Seq Age Sex Outcome Treatment
1 UNK