Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hettich Centrifuge Modules: StreamLAB Centrifuge Module (10372372 or 10444807 or Recalled by Siemens Healthcare Diagnostics Inc. Due to Premature bucket failures
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
Hettich Centrifuge Modules: StreamLAB Centrifuge Module (10372372 or 10444807 or 10706836) Aptio Centrifuge Module (10703032 or 10713761) FlexLab High Throughput Centrifuge Module (11171747) FlexLab and Aptio Centrifuge Module (10628157 or 11266581): Used to separate substances according to their densities.
Quantity: 487
Why Was This Recalled?
Premature bucket failures
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Siemens Healthcare Diagnostics Inc.
Siemens Healthcare Diagnostics Inc. has 10 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report