Class II · Moderate risk
ZTE-1035 Formula
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Is Alfalfa recalled?
Not under an active recall.
Alfalfa was recalled 4 times in the past — all now closed. Most recent: Aug 20, 2021.
Most common reason: Failed specification (3 of these recalls)
Recalls are matched by product description. A recall usually affects specific lots, not every package of Alfalfa. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.
Alfalfa recalls on record
none so far in 2026; 4 on record, newest first
Class II · Moderate risk
Z-103 GU DETOXING. Contents 1000ml 20% Alcohol. WHP Homeopathic…
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Class II · Moderate risk
ZTE-105 Formula Gentle Detoxing. Contents 1000 mL
Out-of-specification test results obtained for identification testing based on HPTLC analysis.
Class I · High risk
Quick Thin
Marketed Without An Approved NDA/ANDA: FDA analysis detected the presence of sibutramine, N-Desmethylsibutramine and phenolphthalein. Sibutramine and phenolphthalein were previously available drug products but were removed from the U.S. market making these products unapproved new drugs.
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