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 2018-06-06 for CLINICAL CHEMISTRY CALCIUM 3L79-21 03L79-21 manufactured by Abbott Manufacturing Inc.
[110583451]
An evaluation is in process. A follow-up report will be submitted when the evaluation is complete. There is no further patient information provided by the customer.
Patient Sequence No: 1, Text Type: N, H10
[110583452]
The customer reported falsely decreased calcium (ca) results on one patient. The results provided were: initial draw = 1. 39mmol/l / repeat = 1. 38mmol/l / new draw same day = 2. 25mmol/l / retest of original sample = 2. 32mmol/l. There was no reported impact to patient management.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1628664-2018-00222 |
MDR Report Key | 7573682 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2018-06-06 |
Date of Report | 2018-09-06 |
Date Mfgr Received | 2018-08-20 |
Device Manufacturer Date | 2017-08-15 |
Date Added to Maude | 2018-06-06 |
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 |
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 | 2018-06-06 |
Model Number | 3L79-21 |
Catalog Number | 03L79-21 |
Lot Number | 20039UN17 |
Device Expiration Date | 2018-07-18 |
Operator | HEALTH PROFESSIONAL |
Device Availability | * |
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 | 2018-06-06 |