FDA Adverse Event
Malfunction
Summary report: N
ACCU-CHEK GUIDE TEST STRIPS
MDR report key: 12023704
·
Received June 18, 2021
Report
- Report Number
- 3011393376-2021-01860
- Event Type
- Malfunction
- Date Received
- June 18, 2021
- Date of Event
- June 6, 2021
- Report Date
- July 1, 2021
- Manufacturer
- ROCHE DIABETES CARE, INC.
- Product Code
- NBW
- UDI-DI
- 00365702719101
- PMA / PMN Number
- K160944
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OH, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
IT WAS REPORTED THE PATIENT RECEIVED THE FOLLOWING RESULTS WITHIN 15 MINUTES ON (B)(6) 2021: 379 MG/DL, 140 MG/DL AND 134 MG/DL. ON (B)(6) 2021, THE CUSTOMER RECEIVED READINGS OF 56 MG/DL, 118 MG/DL AND 140 MG/DL WITHIN 15 MINUTES.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 925213 | ACCU-CHEK GUIDE TEST STRIPS | BLOOD GLUCOSE MONITORING TEST STRIPS | NBW | ROCHE DIABETES CARE, INC. | 08256292001 | 101720 | 00365702719101 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 65 YR |