MAUDE Adverse Event Report: ROCHE DIAGNOSTICS COAGUCHEK ® XS PLUS SYSTEM; PROTHROMBIN TIME TEST STRIPS

Catalog Number 05110157001

Device Problem Improper Device Output (2953)

Patient Problem No Known Impact Or Consequence To Patient (2692)

Event Date 05/08/2015

Event Type  malfunction  

Event Description

Patient tested 2.3 inr on the coaguchek xs system and 3.0 inr twice on the coaguchek xs plus system.No actions taken based on device results.No adverse event reported.Requested return of suspect system and replacement was sent.

Manufacturer Narrative

This event occurred in (b)(6).While this product is not sold in the united states, it is like or similar to a product marketed in the united states the medwatch with identifier (b)(6) is for coaguchek xs plus system 2.Please see medwatch with identifier (b)(6) for coaguchek xs, system 2.

• Brand Name: COAGUCHEK ® XS PLUS SYSTEM
• Type of Device: PROTHROMBIN TIME TEST STRIPS
• Manufacturer (Section D): ROCHE DIAGNOSTICS; 9115 hague road; indianapolis IN 46250
• Manufacturer (Section G): ROCHE DIAGNOSTICS GMBH; sandhoferstrasse 116; na; mannheim 6830 5; GM 68305
• Manufacturer Contact: michael leslie ; 9115 hague road; na; indianapolis, IN 46250 ; 3175214343
• MDR Report Key: 4809466
• MDR Text Key: 5926265
• Report Number: 1823260-2015-03569
• Device Sequence Number: 1
• Product Code: GJS
• Combination Product (y/n): N
• Reporter Country Code: SZ
• PMA/PMN Number: NA
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Other,Foreign,Company Representative
• Reporter Occupation: Medical Equipment Company Technician/Representative
• Type of Report: Initial,Followup
• Report Date: 06/12/2015

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Medical Assistant
• Device Catalogue Number: 05110157001
• Device Lot Number: ASKU
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Initial Date Manufacturer Received: 05/08/2015
• Initial Date FDA Received: 06/01/2015
• Supplement Dates Manufacturer Received: Not provided
• Supplement Dates FDA Received: 06/12/2015
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1