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Precision Dose Recalls
8 recalls on record · April 24, 2013 to July 29, 2026 · Drugs
Recalls by year
13
17
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21
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 29, 2026DrugsFDA
Precision Dose Inc. recalls Glycopyrrolate Oral Solution, 1 mg/5 mL, delivers 5 mL, Rx only, Pkg: Precision Dose, Inc, S. Beloil, IL 61080, unit-dos
Hazard: Failed Impurities/Degradation Specifications
November 17, 2021DrugsFDA
Precision Dose Inc. recalls Acetaminophen Oral Suspension, 325 mg/10.15 mL, packaged in 10.15 mL per cup (NDC Individual cup: 68094-330-59), in a)
Hazard: cGMP Deviations: Product manufactured with contaminated raw ingredient.
November 17, 2021DrugsFDA
Precision Dose Inc. recalls Acetaminophen Oral Suspension, 160 mg/5 mL, packaged in 5 mL per cup (NDC Individual cup: 68094-231-59), in a) 30-count
Hazard: cGMP Deviations: Product manufactured with contaminated raw ingredient.
January 20, 2021DrugsFDA
Precision Dose Inc. recalls Chlorhexidine Gluconate Oral Rinse USP 0.12%, packaged in a) 15 mL x 30 Unit Dose Cups (30-pack case) NDC 68094-028-61,
Hazard: cGMP deviations: The firm was notified of the manufacturer's expanded recall.
March 18, 2020DrugsFDA
Precision Dose Inc. recalls Ranitidine Oral Solution, USP, 150 mg/10 mL, [10 mL x 30 Unit Dose Cups per case, NDC: 68094-204-62; 10 mL x 100 Unit Do
Hazard: CGMP Deviations: Impurity N-nitrosodimethylamine (NDMA) found in API.
November 8, 2017DrugsFDA
Precision Dose Inc. recalls Carbamazepine Oral Suspension USP, 100 mg/5 mL, 5 mL Unit Dose Cups (NDC 68094-301-59), packaged in 10-count cups per tr
Hazard: Subpotent Drug: low out of specification results.
August 9, 2017DrugsFDA
Precision Dose Inc. recalls Carbamazepine Oral Suspension, USP. 100 mg/5 mL, 5 mL Unit Dose Cups, Rx Only, Pkg: Precision Dose, Inc., S. Beloit, IL
Hazard: Labeling Error: Label mix-up. Products' unit dose cups are correctly labeled, but the product carton lists incorrect volume and NDC.
April 24, 2013DrugsFDA
Precision Dose Inc. recalls Children's Acetaminophen Oral Suspension, 650 mg/20.3 mL unit dose cup (NDC 68094-650-59), packaged in 30-count cups per
Hazard: Labeling: Not Elsewhere Classified: This unit dose product is being recalled because the product's name includes the word "Children's" which is misleading since the 650 mg dose of acetaminophen contained within it, is an adult dose.