Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Siemens Acute Care CKMB TestPak- in vitro diagnostic test for Recalled by Siemens Healthcare Diagnostics Inc Due to Stratus CS Cartridge Barcode labels may not scan...
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
Siemens Acute Care CKMB TestPak- in vitro diagnostic test for the measurement of the MB isoenzyme of creatine kinase (ATP: Creatine NPhosphostransferase, E. C. No. 2.7 .3.2) in heparinized plasma Catalog Number: CCKMB SMN:10445068
Quantity: 1051
Why Was This Recalled?
Stratus CS Cartridge Barcode labels may not scan on the Stratus CS systems
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Siemens Healthcare Diagnostics Inc
Siemens Healthcare Diagnostics Inc has 75 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report