MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-02-21 for ALINITY I INSULIN 04T75-20 manufactured by Abbott Germany.
[137128179]
All available patient information was included. Additional patient details are not available. An evaluation is in process. A follow up report will be submitted when the evaluation is complete.
Patient Sequence No: 1, Text Type: N, H10
[137128180]
The customer observed falsely elevated insulin results on the alinity analyzer. The following data was provided: sid (b)(6): initial 2. 7, repeats >300 >600, >3,300 compared to another method as 20-30 uu/ml. A new sample was drawn and results in 18. 9, 15. 8 (matching the other method). There was no impact to patient management reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3002809144-2019-00067 |
MDR Report Key | 8358442 |
Date Received | 2019-02-21 |
Date of Report | 2019-04-01 |
Date Mfgr Received | 2019-03-29 |
Device Manufacturer Date | 2018-08-01 |
Date Added to Maude | 2019-02-21 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | NOEMI ROMERO-KONDOS, RN BSN |
Manufacturer Street | 100 ABBOTT PARK ROAD DEPT. 09B9, LCCP1-3 |
Manufacturer City | ABBOTT PARK IL 600643537 |
Manufacturer Country | US |
Manufacturer Postal | 600643537 |
Manufacturer Phone | 224667-512 |
Manufacturer G1 | ABBOTT GERMANY |
Manufacturer Street | MAX-PLANCK-RING 2 |
Manufacturer City | WIESBADEN 65205 |
Manufacturer Country | GM |
Manufacturer Postal Code | 65205 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | ALINITY I INSULIN |
Generic Name | INSULIN |
Product Code | CFP |
Date Received | 2019-02-21 |
Catalog Number | 04T75-20 |
Lot Number | 93511LP16 |
Device Expiration Date | 2019-05-30 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ABBOTT GERMANY |
Manufacturer Address | MAX-PLANCK-RING 2 WIESBADEN 65205 GM 65205 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-02-21 |