Belladonna Alkaloids (hyoscyamine recalls

The FDA has published 1 recall involving Belladonna Alkaloids (hyoscyamine since 2013. The latest was reported on 6 Mar 2013. Most were for packaging defects. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.

Total recalls1since 2013

Last 12 months0reported

Class I00% of total

Ongoing0latest 6 Mar 2013

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 1 100%Class III 0 0%

Why belladonna alkaloids (hyoscyamine is recalled

Packaging Defects1100%

Companies

West-ward Pharmaceutical1100%

By year

20131100%

All belladonna alkaloids (hyoscyamine recalls, newest first

1 total

Reported	Class	Recall	Company	Reason	Where
6 Mar 2013Drug	CLASS II	Belladonna Alkaloids (hyoscyamine sulfate, USP 0.1037 mg recalled	West-ward Pharmaceutical	Packaging Defects	Nationwide

Should you stop taking Belladonna Alkaloids (hyoscyamine?

Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.