MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-09-17 for ARCHITECT IVANCOMYCIN 01P30-27 manufactured by Abbott Germany.
[120839814]
An evaluation is in process. A follow-up report will be submitted when the evaluation is complete. This report is being filed on an international product, list number 1p30-27 that has a similar product distributed in the us, list number 1p30-28. An evaluation is in process.
Patient Sequence No: 1, Text Type: N, H10
[120839815]
The customer observed falsely depressed results while using architect ivancomycin reagents. The following data was provided. Sid (b)(6) initial (tested 9:25 a. M. ) 0. 24 ug/ml, repeat (tested 10:00 a. M. ) 64. 78 ug/ml. No impact to patient management was reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3002809144-2018-00345 |
MDR Report Key | 7882946 |
Date Received | 2018-09-17 |
Date of Report | 2018-10-26 |
Date of Event | 2018-08-27 |
Date Mfgr Received | 2018-10-10 |
Device Manufacturer Date | 2018-02-01 |
Date Added to Maude | 2018-09-17 |
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 | ARCHITECT IVANCOMYCIN |
Generic Name | VANCOMYCIN |
Product Code | LEH |
Date Received | 2018-09-17 |
Catalog Number | 01P30-27 |
Lot Number | 00118A000 |
Device Expiration Date | 2019-06-21 |
Operator | HEALTH PROFESSIONAL |
Device Availability | * |
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 | 2018-09-17 |