FDA Adverse Event
Summary report: N
TIMEX
MDR report key: 500958
·
Received December 3, 2003
Report
- Report Number
- MW1030427
- Date Received
- December 3, 2003
- Manufacturer
- TIMEX
- Product Code
- FLK
- Report Source
- Voluntary report
- Reporter Occupation
- PATIENT
Narratives
Description of Event or Problem · 1
REPORTER RECENTLY PURCHASED THIS PRODUCT AND IN THEIR OPINION IT SHOULD NOT BE SOLD ON THE MARKET. THE THERMOMETER DID NOT READ THE TEMPERATURE AFTER FLEXING THE TIP AS INDICATED ON THE PACKAGE. RPTR FEELS THAT IF IT IS A GOOD PRODUCT IT SHOULD WORK AS NOTED. RPTR ASKS IF IT IS EVEN ACCURATE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TIMEX | * | FLK | TIMEX | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |