Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Citalopram Oral Solution Recalled by PAI Holdings, LLC. dba Pharmaceutical Associates Inc Due to Failed Impurities/Degradation Specifications; high out of specification results...
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 PAI Holdings, LLC. dba Pharmaceutical Associates Inc directly.
Affected Products
Citalopram Oral Solution, USP 20 mg/10 mL, 10 mL unit dose cups, Rx Only, Mfg for: Pharmaceutical Associates, Inc. Greenville, SC 29605 NDC 0121-1696-40
Quantity: 13480 cups
Why Was This Recalled?
Failed Impurities/Degradation Specifications; high out of specification results obtained at the 9 month stability timepoint
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About PAI Holdings, LLC. dba Pharmaceutical Associates Inc
PAI Holdings, LLC. dba Pharmaceutical Associates Inc has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report