FDA Adverse Event Malfunction Summary report: N

RSP

MDR report key: 223769 · Received May 13, 1999

Report

Report Number
MW1016329
Event Type
Malfunction
Date Received
May 13, 1999
Date of Event
May 1, 1999
Report Date
May 13, 1999
Manufacturer
RESPIRATORY SUPPORT PRODUCTS, INC.
Product Code
FLL
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
TX, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

PROBE WOULD NOT ALLOW BED TO HEAT. AFTER USING ANOTHER PROBE THE BED WORKED FINE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 RSP NEO-THERM SKIN TEMPERATURE SENSOR FLL RESPIRATORY SUPPORT PRODUCTS, INC. * 1252

Patients

Seq Age Sex Outcome Treatment
1 * Other NOT APPLICABLE.