MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2019-02-12 for CLINICAL CHEMISTRY CALCIUM 03L79-21 manufactured by Abbott Manufacturing Inc.
[137137767]
Patient information: patient identifier = sid (b)(6). 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
[137137768]
The customer reported falsely depressed calcium (ca) results on one patient generated on the architect analyzer. The results provided were: sid (b)(6) initial = 2. 4mg/dl / repeated on different analyzer = 8. 7mg/dl. There was no reported impact to patient management.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1628664-2019-00118 |
MDR Report Key | 8332065 |
Report Source | HEALTH PROFESSIONAL |
Date Received | 2019-02-12 |
Date of Report | 2019-03-12 |
Date Mfgr Received | 2019-02-19 |
Date Added to Maude | 2019-02-12 |
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 | 2019-02-12 |
Catalog Number | 03L79-21 |
Lot Number | UNKNOWN |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | N |
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 | 2019-02-12 |