Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Carbamazepine Oral Suspension USP Recalled by Precision Dose Inc. Due to Subpotent Drug: low 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 Precision Dose Inc. directly.
Affected Products
Carbamazepine Oral Suspension USP, 100 mg/5 mL, 5 mL Unit Dose Cups (NDC 68094-301-59), packaged in 10-count cups per tray, 3 trays per case containing a total of 5 mL x 30 Unit Dose Cups per case (NDC 68094-301-62), Rx only, Pkg: Precision Dose, Inc., S. Beloit, IL 61080.
Quantity: 801 cases
Why Was This Recalled?
Subpotent Drug: low out of specification results.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Precision Dose Inc.
Precision Dose 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