Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Turbo Troponin I For in vitro diagnostic use for the Recalled by Siemens Healthcare Diagnostics, Inc. Due to
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Siemens Healthcare Diagnostics, Inc. directly.
Affected Products
Turbo Troponin I For in vitro diagnostic use for the quantitative measurement of troponin I in serum, heparinized or EDTA plasma, as an aid in the diagnosis of acute myocardial infarction (AMI).
Quantity: 3,622 kits (3,572 domestic and 50 internationally)
Why Was This Recalled?
Where Was This Sold?
This product was distributed to 5 states: CO, FL, MN, MT, NY
About Siemens Healthcare Diagnostics, Inc.
Siemens Healthcare Diagnostics, Inc. has 452 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report