MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2018-09-20 for CLINICAL CHEMISTRY CARBON DIOXIDE 03L80-31 manufactured by Abbott Manufacturing Inc.
[120978420]
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
[120978421]
The account generated a falsely elevated patient result for architect carbon dioxide and when repeated was normal. The customer provided (b)(6): initial result 33 meq/l and same day repeat result 28 meq/l (account normal range 23-31meq/l). No impact to patient management reported. The account does not know specific patient information.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1628664-2018-01894 |
MDR Report Key | 7895185 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2018-09-20 |
Date of Report | 2019-01-22 |
Date of Event | 2018-09-05 |
Date Mfgr Received | 2018-12-26 |
Device Manufacturer Date | 2018-05-18 |
Date Added to Maude | 2018-09-20 |
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 CARBON DIOXIDE |
Generic Name | CARBON DIOXIDE |
Product Code | KHS |
Date Received | 2018-09-20 |
Catalog Number | 03L80-31 |
Lot Number | 52780UQ04 |
Device Expiration Date | 2019-05-31 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
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 | 2018-09-20 |