Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Syva¿ EMIT¿ II Plus 6-Acetyl morphine Catalog # for 28 Recalled by Siemens Healthcare Diagnostics, Inc. Due to Incorrect calibrator level listed in qualitative calibration steps
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
Syva¿ EMIT¿ II Plus 6-Acetyl morphine Catalog # for 28 mL: 9R039UL /SMN# 10470440
Quantity: N/A
Why Was This Recalled?
Incorrect calibrator level listed in qualitative calibration steps
Where Was This Sold?
This product was distributed to 9 states: FL, KS, KY, ME, MA, NH, PA, TX, UT
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