Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
CABERGOLINE Tablets Recalled by Teva Pharmaceuticals USA, Inc. Due to Impurities/Degradation Products: This lot of product will not...
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
CABERGOLINE Tablets, 0.5 mg, RX only, 8 count bottles, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960 NDC 0093-5420-88
Quantity: 13,232 bottles
Why Was This Recalled?
Impurities/Degradation Products: This lot of product will not meet the impurity specification over shelf life
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