Siemens Healthcare Diagnostics, Inc. recalls Syva¿ EMIT¿ II Plus 6-Acetylmorphine Catalog # for 1000 mL: 9R129UL /SMN# 10481483
- Recall date
- March 12, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1799-2018
- FDA classification
- Class III
- Brand / firm
- Siemens Healthcare Diagnostics, Inc.
- Sold / distributed
- PA, MA, TX, ME, UT, FL, KS, NH, KY and Foreign
Why it was recalled
Incorrect calibrator level listed in qualitative calibration steps
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Syva¿ EMIT¿ II Plus 6-Acetylmorphine Catalog # for 1000 mL: 9R129UL /SMN# 10481483
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