FDA Adverse Event
Malfunction
Summary report: N
SURESTEP
MDR report key: 237999
·
Received August 25, 1999
Report
- Report Number
- 2939301-1999-00651
- Event Type
- Malfunction
- Date Received
- August 25, 1999
- Report Date
- July 26, 1999
- Manufacturer
- LIFESCAN, INC.
- Product Code
- CGA
- Removal / Correction Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NJ, US
- Reporter Occupation
- PATIENT
Narratives
Additional Manufacturer Narrative · 1
METER WAS NOT THE SUBJECT OF FDA RECALL Z-631-8
Description of Event or Problem · 1
THE RPTR DID BACK TO BACK BLOOD GLUCOSE TESTS AND GOT RESULTS OF 103, 118, 192 AND 214 MG/DL. TESTS WERE DONE WITHIN 10 MINS, USING DIFFERENT FINGERSTICKS. THERE WERE NO SYMPTOMS. A CONTROL SOLUTION TEST WAS WITHIN RANGE 130 (96-144).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SURESTEP | BLOOD GLUCOSE MONITORING KIT/SYSTEM | CGA | LIFESCAN, INC. | NA | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 74 YR | Other |