FDA Adverse Event Other Summary report: N

3CC SAF. SYR 20X1-1/2

MDR report key: 318691 · Received March 1, 2001

Report

Report Number
1650158-2001-00001
Event Type
Other
Date Received
March 1, 2001
Date of Event
January 9, 2001
Report Date
February 23, 2001
Manufacturer
KENDALL HEALTHCARE PRODUCTS
Product Code
MEG
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

IT WAS REPORTED TO KENDALL HEALTHCARE PRODUCTS IN 2/2001 THAT LPN WENT TO GIVE INJECTION AND THE SHIELD FELL BACK. LPN STATES THAT LPN HAS HAD EXPERIENCE WITH THEM AND NEVER HAD THIS PROBLEM. LPN IS ALMOST SURE LPN LOCKED IT BUT CANNOT SAY FOR SURE. SAMPLE WAS DISPOSED OF.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
8683 3CC SAF. SYR 20X1-1/2 SAFETY SYRINGE MEG KENDALL HEALTHCARE PRODUCTS * 707908 OR 705057

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN Other