Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Is Belladonna recalled?

Not under an active recall. Belladonna was recalled 9 times in the past — all now closed. Most recent: Aug 20, 2021.

Most common reason: Particulate / foreign matter (4 of these recalls)

Recalls are matched by product description. A recall usually affects specific lots, not every package of Belladonna. “Active” means an FDA recall is still ongoing; “closed” means it was terminated or completed. Checked against openFDA on Oct 10, 2026.

Belladonna recalls on record

none so far in 2026; 9 on record, newest first
Class I · High risk

Hyland's Baby Nighttime Teething Tablets

Superpotent Drug: FDA analysis found inconsistent amounts of belladonna alkaloids that may differ from the calculated amount on the product labels.

Terminated Wrong potency / content Standard Homeopathic Company NDC 54973-3197-1 D-0864-2017
Class I · High risk

Hyland's Baby Teething Tablets

Superpotent Drug: FDA analysis found inconsistent amounts of belladonna alkaloids that may differ from the calculated amount on the product labels.

Terminated Wrong potency / content Standard Homeopathic Company NDC 54973-3127-3 D-0863-2017
Class II · Moderate risk

Belladonna Extract Powder active pharmaceutical ingredient…

Penicillin Cross Contamination: All lots of all products repackaged and distributed between 01/05/12 and 02/12/15 are being recalled because they were repackaged in a facility with penicillin products without adequate separation which could introduce the potential for cross contamination with penicillin.

Terminated Cross-contamination Attix Pharmaceuticals D-535-2015
Class II · Moderate risk

Belladonna Alkaloids/PB

Presence of Foriegn Substance:The manufacturer, West-ward Pharmaceutical, recalled product because of the presence of black spots on tablets. In response, the repackager initiated its own recall.

Terminated Particulate / foreign matter Physicians Total Care, Inc. NDC 54868-0031-04 D-826-2013
Class II · Moderate risk

Belladonna Alkaloids

Presence of Foreign Substance: Uncharacteristic blacks spots were found in tablets.

Terminated Particulate / foreign matter West-ward Pharmaceutical Corp. NDC 0143-1140-10 D-170-2013