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 2017-12-26 for ALNTY C CREATININE 3000 07P99-20 manufactured by Abbott Manufacturing Inc.
[95871381]
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 07p99, which has a similar product distributed in the us, list number 03l81.
Patient Sequence No: 1, Text Type: N, H10
[95871382]
The customer reports that one patient sample (sid (b)(6)) generated an initial alinity creatinine assay result of 3. 37 mg/dl on an alinity c processing module. The sample retested at 0. 69 mg/dl. No suspect results were reported from the lab. There is no impact to patient management reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1628664-2017-00534 |
MDR Report Key | 7146078 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2017-12-26 |
Date of Report | 2018-01-19 |
Date of Event | 2017-12-04 |
Date Mfgr Received | 2018-01-10 |
Date Added to Maude | 2017-12-26 |
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 | ALNTY C CREATININE 3000 |
Generic Name | CREATININE |
Product Code | CGX |
Date Received | 2017-12-26 |
Catalog Number | 07P99-20 |
Lot Number | 12798UN17 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
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 | 2017-12-26 |