Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Intermezzo (zolpidem tartrate) Recalled by Purdue Pharma L.P. Due to Failed dissolution 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 Purdue Pharma L.P. directly.
Affected Products
Intermezzo (zolpidem tartrate), sublingual tablet 3.5 mg, 1 tablet per pouch, 30 pouches per carton, Rx only, Distributed by Purdue Pharma L.P. Stamford, CT 06901-3431, NDC 59011-265-30
Quantity: 6,264 cartons (30 sublingual tablets in 1 carton)
Why Was This Recalled?
Failed dissolution specifications
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Purdue Pharma L.P.
Purdue Pharma L.P. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report