FDA Adverse Event Malfunction Summary report: N

ALLIED HEALTHCARE PRODUCTS, INC.

MDR report key: 502020 · Received December 5, 2003

Report

Report Number
MW1030522
Event Type
Malfunction
Date Received
December 5, 2003
Report Date
December 5, 2003
Manufacturer
ALLIED HEALTHCARE PRODUCTS, INC.
Product Code
CCQ
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
OR, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Description of Event or Problem · 1

PACKAGING FOR AEROMIST NEBULIZER IS INFERIOR AND TEARS OPEN AT PERFORATION WHEN LIGHTLY TOUCHED LEAVING NEBULIZER EXPOSED TO OPEN AND RESULTS IN CONTENTS FALLING OUT OF PACKAGING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ALLIED HEALTHCARE PRODUCTS, INC. AERMOIST NEBULIZER CCQ ALLIED HEALTHCARE PRODUCTS, INC. * *

Patients

Seq Age Sex Outcome Treatment
1 *