FDA Adverse Event Malfunction Summary report: N

LIFE SUPPORT PRODUCTS

MDR report key: 97956 · Received June 12, 1997

Report

Report Number
97956
Event Type
Malfunction
Date Received
June 12, 1997
Report Date
June 11, 1997
Manufacturer
ALLIED HEALTHCARE PRODUCTS, INC.
Product Code
CAN
Product Problem
Yes
Report Source
User Facility report
Reporter Location
IL, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

DEVICE RECALL BY ALLIED HEALTHCARE PRODUCTS OF INLET FILTERS FOR MODEL L270-020 AND L270-050 OXYGEN REGULATORS MFG BY LIFE SUPPORT PRODUCTS, INC.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 LIFE SUPPORT PRODUCTS OXYGEN FLOW REGULATOR CAN ALLIED HEALTHCARE PRODUCTS, INC. L270-020 AND L270-050 *

Patients

Seq Age Sex Outcome Treatment
1 *