Class II · Moderate risk Terminated
Brompheniramine/Pseudoephedrine Dm
Reason CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Is Histamine recalled?
Yes — there is an active recall. 4 ongoing FDA recalls mention Histamine (109 total). Check the affected lots below.
Recalls are matched by product description. A recall usually affects specific lots, not every package of Histamine. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed.
Class II · Moderate risk Terminated
Dallergy CHEWABLE TABLETS
Reason CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Class II · Moderate risk Terminated
Dallergy TABLETS
Reason CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Class II · Moderate risk Terminated
NoHist TABLETS
Reason CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Class II · Moderate risk Terminated
Ed A-Hist Tablets
Reason CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Class II · Moderate risk Terminated
Ambi 3brm/30dm/50pse
Reason CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Class II · Moderate risk Terminated
Ambi 3brm/15dm/30pse
Reason CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Class II · Moderate risk Terminated
Ambi 2cpm/15dm/5peh
Reason CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
Class II · Moderate risk Terminated
Ambi 25dph/7.5peh
Reason CGMP Deviations: Products are underdosed or have an incorrect dosage regime.
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