Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Cefdinir for Oral Suspension Recalled by Teva Pharmaceuticals USA, Inc. Due to Defective Container: This recall is being carried out...
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 Teva Pharmaceuticals USA, Inc. directly.
Affected Products
Cefdinir for Oral Suspension, 125 mg/5 mL, packaged in a) 60 mL bottle (NDC 0093-4136-64); b) 100 mL bottle (NDC 0093-4136-73), Rx only, Teva Pharmaceuticals USA, Sellersville, PA 18960.
Quantity: 62,187 bottles
Why Was This Recalled?
Defective Container: This recall is being carried out due to the potential for improperly sealed bottles.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Teva Pharmaceuticals USA, Inc.
Teva Pharmaceuticals USA, Inc. has 33 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report