PlainRecalls
FDA Devices Moderate Class II Terminated

Stratus CS Acute Care cTNI TestPak, SMN 10445071 Product Usage: In vitro diagnostic test for the measurement of cardiac troponin I in heparinized plasma. Cardiac troponin I measurements can be used as an aid in the diagnosis of acute myocardial infarction (AMI).

Reported: August 7, 2019 Initiated: May 29, 2019 #Z-2135-2019

Product Description

Stratus CS Acute Care cTNI TestPak, SMN 10445071 Product Usage: In vitro diagnostic test for the measurement of cardiac troponin I in heparinized plasma. Cardiac troponin I measurements can be used as an aid in the diagnosis of acute myocardial infarction (AMI).

Reason for Recall

Potential for increased rate of false positive results and/or increased rate of random non-repeatable false positive results.

Details

Units Affected
2312
Distribution
US Nationwide Distribution
Location
Norwood, MA

Frequently Asked Questions

What product was recalled?
Stratus CS Acute Care cTNI TestPak, SMN 10445071 Product Usage: In vitro diagnostic test for the measurement of cardiac troponin I in heparinized plasma. Cardiac troponin I measurements can be used as an aid in the diagnosis of acute myocardial infarction (AMI).. Recalled by Siemens Healthcare Diagnostics Inc. Units affected: 2312.
Why was this product recalled?
Potential for increased rate of false positive results and/or increased rate of random non-repeatable false positive results.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 7, 2019. Severity: Moderate. Recall number: Z-2135-2019.