Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Atelia IM 1300 Analyzer for in vitro diagnostic testing of clinical specimens. Recalled by Siemens Healthcare Diagnostics, Inc. Due to When more than one immunoassay analyzer is connected...
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
Atelia IM 1300 Analyzer for in vitro diagnostic testing of clinical specimens.
Quantity: N/A
Why Was This Recalled?
When more than one immunoassay analyzer is connected to a single solution system, reporting and conversion factors may not be applied to all analyzers
Where Was This Sold?
This product was distributed to 1 state: FL
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