FDA Adverse Event Malfunction Summary report: N

ACCUSURE

MDR report key: 1410758 · Received July 2, 2009

Report

Report Number
1039144-2009-00011
Event Type
Malfunction
Date Received
July 2, 2009
Report Date
July 2, 2009
Manufacturer
SHIN CHANG MEDICAL CO., LTD.
Product Code
FMF
Product Problem
Yes
Report Source
Distributor report
Reporter Location
HI, US
Reporter Occupation
PHARMACIST

Narratives

Description of Event or Problem · 1

NEEDLES WERE BREAKING UPON ADMINISTRATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ACCUSURE INSULIN SYRINGE FMF SHIN CHANG MEDICAL CO., LTD. 0603-7002-21 SD0314

Patients

Seq Age Sex Outcome Treatment
1 UNK