Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Belladonna Alkaloids (hyoscyamine sulfate Recalled by West-ward Pharmaceutical Corp. Due to Presence of Foreign Substance: Uncharacteristic blacks spots were...

Date: January 7, 2013
Company: West-ward Pharmaceutical Corp.
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact West-ward Pharmaceutical Corp. directly.

Affected Products

Belladonna Alkaloids (hyoscyamine sulfate, USP 0.1037 mg; atropine sulfate, USP 0.0194 mg; scopolamine HBr, USP 0.0065 mg) with Phenobarbital (USP 16.2 mg) Tablets, packaged in a) 1000-count tablets per bottle (NDC 0143-1140-10; b) 5000-count tablets per bottle (NDC 143-1140-51); Rx only, Manufactured by: West-ward Pharmaceutical Corp. Eatontown, NJ 07724

Quantity: 6,511 bottles

Why Was This Recalled?

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

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About West-ward Pharmaceutical Corp.

West-ward Pharmaceutical Corp. has 17 total recalls tracked by RecallDetector.

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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report