Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Atellica CH Reaction Ring Segment Recalled by Siemens Healthcare Diagnostics, Inc. Due to Some lots ending in "17", "18", "19", or...
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
Atellica CH Reaction Ring Segment, SMN 11099326, UDI 00630414596143
Quantity: 3559
Why Was This Recalled?
Some lots ending in "17", "18", "19", or higher may have cuvette defects allowing water from the water bath to contaminate the interior of the cuvette, which may falsely elevate or depress sample results.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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