MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2018-10-17 for CLINICAL CHEMISTRY CALCIUM 03L79-21 manufactured by Abbott Manufacturing Inc.
[126096589]
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
[126096590]
The customer reported multiple false elevated architect calcium results on the architect c16000 analyzer. Sample id 9175964jp generated an initial result of 5. 13 mmol/l and retest of 2. 20 mmol/l. No adverse impact to patient management was reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1628664-2018-01946 |
MDR Report Key | 7975515 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2018-10-17 |
Date of Report | 2019-01-29 |
Date of Event | 2018-09-25 |
Date Mfgr Received | 2019-01-25 |
Device Manufacturer Date | 2018-04-03 |
Date Added to Maude | 2018-10-17 |
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 MANUFACTURING INC |
Manufacturer Street | 1921 HURD DRIVE |
Manufacturer City | IRVING TX 75038 |
Manufacturer Country | US |
Manufacturer Postal Code | 75038 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CLINICAL CHEMISTRY CALCIUM |
Generic Name | CALCIUM |
Product Code | CJY |
Date Received | 2018-10-17 |
Catalog Number | 03L79-21 |
Lot Number | 98314UN17 |
Device Expiration Date | 2019-02-27 |
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 MANUFACTURING INC |
Manufacturer Address | 1921 HURD DRIVE IRVING TX 75038 US 75038 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2018-10-17 |