Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Mirapex (pramipexole dihydrochloride) Tablets Recalled by Boehringer Ingelheim Pharmaceuticals, Inc. Due to Failed Tablet/Capsule Specifications: identification of low weight tablets...
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 Boehringer Ingelheim Pharmaceuticals, Inc. directly.
Affected Products
Mirapex (pramipexole dihydrochloride) Tablets, 1 mg, 100-count unit-dose tablets per folding carton, Rx only, Distributed by: Boehringer Ingelheim (BI) Pharmaceuticals, Inc., Ridgefield, CT 06877 USA, Made in Germany, NDC 0597-0190-61.
Quantity: 112 folding cartons
Why Was This Recalled?
Failed Tablet/Capsule Specifications: identification of low weight tablets during routine stability testing.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Boehringer Ingelheim Pharmaceuticals, Inc.
Boehringer Ingelheim Pharmaceuticals, Inc. has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report