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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: ABBOTT POINT OF CARE I-STAT PT/INR CARTRIDGE

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ABBOTT POINT OF CARE I-STAT PT/INR CARTRIDGE Back to Search Results
Catalog Number 03P89-24
Device Problem False Positive Result
Event Date 03/22/2017
Event Type  Malfunction  
Manufacturer Narrative

Apoc incident # (b)(4). Apoc labeling will be evaluated during the investigation as pertaining to the event.

 
Event Description

On 03/25/2017, abbott point of care was contacted by a customer regarding i-stat pt/inr cartridges that yielded suspected discrepant results on a (b)(6) female patient. The patient was on warfarin at the time of testing and was to be transitioned to plavix but unknown if the patient was also on plavix at the time of testing. It was stated that the patient was very ill but the diagnosis is unknown. There was no additional patient information at the time of this report. The customer states that return product is not available for investigation. (b)(6). There are no injuries associated with this event. The investigation is underway.

 
Manufacturer Narrative

Apoc incident # (b)(4). The investigation was completed on 06/29/2017. Retain product was tested and functioning according to specification. Return product was not available for investigation.

 
Event Description

Na.

 
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Brand NameI-STAT PT/INR CARTRIDGE
Type of DevicePT/INR CARTRIDGE
Manufacturer (Section D)
ABBOTT POINT OF CARE
400 college road
princeton NJ 08540 6607
Manufacturer (Section G)
ABBOTT POINT OF CARE CANADA LTD.
185 corkstown road
ottawa, ontario K2H 8 V4
CA  K2H 8V4
Manufacturer Contact
linda maczuszenko
400 college road
princeton , NJ 08540
6136885949
MDR Report Key6449547
Report Number2245578-2017-00017
Device Sequence Number1
Product CodeGJS
Report Source Manufacturer
Source Type HEALTH PROFESSIONAL
Reporter Occupation OTHER HEALTH CARE PROFESSIONAL
Type of Report Initial,Followup
Report Date 07/07/2017
1 Device Was Involved in the Event
0 PatientS WERE Involved in the Event:
Date FDA Received03/31/2017
Is This An Adverse Event Report? No
Is This A Product Problem Report? Yes
Device Operator HEALTH PROFESSIONAL
Device EXPIRATION Date05/14/2017
Device Catalogue Number03P89-24
Device LOT NumberS16322A
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? Yes
Was the Report Sent to FDA?
Event Location No Information
Date Manufacturer Received06/29/2017
Was Device Evaluated By Manufacturer? Yes
Date Device Manufactured11/17/2016
Is The Device Single Use? Yes
Is this a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial

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