FDA Adverse Event
Injury
Summary report: N
TELADOC BLOOD GLUCOSE METER
MDR report key: 23498847
·
Received November 7, 2025
Report
- Report Number
- 3011196194-2025-00099
- Event Type
- Injury
- Date Received
- November 7, 2025
- Date of Event
- October 21, 2025
- Report Date
- November 6, 2025
- Manufacturer
- TELADOC HEALTH INC
- Product Code
- NBW
- PMA / PMN Number
- K133584
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 0
A REPLACEMENT BLOOD GLUCOSE METER WAS SENT. THE DEVICE ASSOCIATED WITH THIS INCIDENT WAS NOT RETURNED FOR INVESTIGATION. IF THE DEVICE IS RETURNED, AN INVESTIGATION WILL BE CONDUCTED AND A SUPPLEMENTAL REPORT WILL BE FILED.
Description of Event or Problem · 0
THE PATIENT REPORTED THAT THEIR BLOOD GLUCOSE METER WAS PROVIDING LOW READINGS. THE PATIENT RECEIVED A LOW READING OF 83 AFTER LUNCH, AND A NURSE RE-CHECKED THEIR BLOOD GLUCOSE USING ANOTHER METER AND OBTAINED A RESULT OF 164. NO TREATMENT WAS PROVIDED AT THE TIME OF THE INACCURATE READING. HOWEVER, THE PATIENT STATED THAT THEIR DOCTOR HAD INCREASED THEIR JARDIANCE DOSAGE IN THE PAST MONTH FROM 2.5 MG TO 7 MG BASED ON BLOOD GLUCOSE METER READINGS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1860981 | TELADOC BLOOD GLUCOSE METER | BLOOD GLUCOSE METER | NBW | TELADOC HEALTH INC | BG300C |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 65 YR | Unknown | Other |