Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Amoxicillin for Oral suspension Recalled by West-Ward Pharmaceuticals Corp. Due to Labeling: Label Error on Declared Strength: Some bottles...
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 Pharmaceuticals Corp. directly.
Affected Products
Amoxicillin for Oral suspension, USP 400 mg/5 mL, 100 mL (when reconstituted), Rx only, Manufactured by: Hikma Pharmaceuticals, P.O. Box 183400, Amman 11118 - Jordan, NDC 0143-9887-01
Quantity: 32,102 bottles
Why Was This Recalled?
Labeling: Label Error on Declared Strength: Some bottles miss a color coded panel where the strength of the product is typically displayed.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About West-Ward Pharmaceuticals Corp.
West-Ward Pharmaceuticals Corp. has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report