Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Zemplar (paricalcitol) capsules Recalled by AbbVie Inc. Due to Failed Content Uniformity Specifications
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 AbbVie Inc. directly.
Affected Products
Zemplar (paricalcitol) capsules, 1 mcg, 30-count bottle, Rx Only, Mfd for AbbVie Inc. North Chicago, IL 60064, NDC 0074-4317-30.
Quantity: 307 bottles
Why Was This Recalled?
Failed Content Uniformity Specifications
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About AbbVie Inc.
AbbVie Inc. has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report