FDA Adverse Event
Malfunction
Summary report: N
AUTODISC 50 TEST STRIPS
MDR report key: 868958
·
Received September 27, 2006
Report
- Report Number
- 1826988-2006-01144
- Event Type
- Malfunction
- Date Received
- September 27, 2006
- Date of Event
- August 23, 2006
- Report Date
- August 23, 2006
- Manufacturer
- BAYER HEALTHCARE, LLC
- Product Code
- NBW
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Description of Event or Problem · 1
THE CONTACT CALLED BECAUSE THE CUSTOMER'S METER KEPT READING "LO". WHILE TROUBLESHOOTING, THE CONTACT PERFORMED 2 NORMAL CONTROL TESTS AND RECEIVED RESULTS OF "LO". THE NORMAL CONTROL RANGE IS 113-162 MG/DL. THE CONTACT DID NOT ALLEGE THE CUSTOMER EXPERIENCED ANY ADVERSE EVENTS. THE TEST STRIPS ARE TO BE RETURNED FOR EVALUATION, AND REPLACEMENT STRIPS WILL BE SENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | AUTODISC 50 TEST STRIPS | BLOOD GLUCOSE TEST STRIPS | NBW | BAYER HEALTHCARE, LLC | 3622A | AA3034AA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | YR |