FDA Adverse Event Other Summary report: N

PEGGY PREEMIE

MDR report key: 171927 · Received June 11, 1998

Report

Report Number
MW1013948
Event Type
Other
Date Received
June 11, 1998
Date of Event
May 27, 1998
Report Date
June 11, 1998
Manufacturer
LAERDAL MEDICAL CORP.
Product Code
LYM
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
TX, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

ADDITIONAL INFO RECEIVED FROM MFR ON 07/28/1998: MFR HAS CONTACTED THE RPTR ABOUT THE REPORT AS LAERDAL DOES NOT HAVE A MANIKIN NAMED PEGGY PREEMIE. RPTR APOLOGIZED AND INFORMED MFR THAT THEY HAD MADE A MISTAKE IN IDENTIFYING THE MFR ON THEIR REPORT. THE PEGGY PREEMIE IS A SIMULAIDS PRODUCT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 PEGGY PREEMIE CPR MANIKIN LYM LAERDAL MEDICAL CORP. UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 30 YR Other