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 |