ALNTY C CREATININE 3000 07P99-20

MAUDE Adverse Event Report

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.

Event Text Entries

[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


MAUDE Entry Details

Report Number1628664-2017-00534
MDR Report Key7146078
Report SourceFOREIGN,HEALTH PROFESSIONAL
Date Received2017-12-26
Date of Report2018-01-19
Date of Event2017-12-04
Date Mfgr Received2018-01-10
Date Added to Maude2017-12-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactNOEMI ROMERO-KONDOS, RN BSN
Manufacturer Street100 ABBOTT PARK ROAD DEPT. 09B9, LCCP1-3
Manufacturer CityABBOTT PARK IL 600643537
Manufacturer CountryUS
Manufacturer Postal600643537
Manufacturer Phone224667-512
Manufacturer G1ABBOTT MANUFACTURING INC
Manufacturer Street1921 HURD DRIVE
Manufacturer CityIRVING TX 75038
Manufacturer CountryUS
Manufacturer Postal Code75038
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameALNTY C CREATININE 3000
Generic NameCREATININE
Product CodeCGX
Date Received2017-12-26
Catalog Number07P99-20
Lot Number12798UN17
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerABBOTT MANUFACTURING INC
Manufacturer Address1921 HURD DRIVE IRVING TX 75038 US 75038


Patients

Patient NumberTreatmentOutcomeDate
10 2017-12-26

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.