FDA Adverse Event Summary report: N

URICULT

MDR report key: 11381 · Received February 8, 1994

Report

Report Number
MW1000677
Date Received
February 8, 1994
Date of Event
January 13, 1994
Manufacturer
ORION DIAGNOSTICA, INC.
Product Code
JXA
Report Source
Voluntary report
Reporter Location
AR, US
Reporter Occupation
PHARMACIST

Narratives

Description of Event or Problem · 1

TOO MUCH MOISTURE INSIDE TUBES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 URICULT JXA ORION DIAGNOSTICA, INC. TK022

Patients

Seq Age Sex Outcome Treatment
1 *