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)
Recalled November 17, 2021 · FDA recall D-0095-2022 · Precision Dose
Hazard
cGMP Deviations: Product manufactured with contaminated raw ingredient. · FDA Class II
Units
151,100 unit dose cups
Sold at
Nationwide USA
Description
cGMP Deviations: Product manufactured with contaminated raw ingredient.
Product
Acetaminophen Oral Suspension, 325 mg/10.15 mL, packaged in 10.15 mL per cup (NDC Individual cup: 68094-330-59), in a) 30-count case (NDC 30-count case: 68094-330-62), and b) 100-count case (NDC 100-count case: 68094-330-61), Hospital Use Only, Pkg. Precision Dose, Inc., S. Beloit, IL 61080.
Manufacturer(s)
Precision Dose Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →