Aconitum Napellus 12X Fear* 87% Alcohol HPUS: packaged in 30 mL containers
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Most common reason: Failed specification (7 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Aconitum. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
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