VistaPharm, Inc. recalls Hydrocodone Bitartrate and Acetaminophen Oral Solution 7.5 mg/325 mg per 15 mL (Cherry Flavored), 473 mL bottles, Rx onl

Recalled September 20, 2017 · FDA recall D-1139-2017 · VistaPharm

Hazard

Labeling: Not Elsewhere Classified; product is incorrectly labeled as Class III controlled substance instead of Class II controlled substance · FDA Class III

Units

3084 bottles

Sold at

Nationwide

Description

Labeling: Not Elsewhere Classified; product is incorrectly labeled as Class III controlled substance instead of Class II controlled substance

Product

Hydrocodone Bitartrate and Acetaminophen Oral Solution 7.5 mg/325 mg per 15 mL (Cherry Flavored), 473 mL bottles, Rx only, Manufactured by: VistaPharm, Inc. Largo, FL 33771 ---- NDC 66689-023-16

Manufacturer(s)

VistaPharm, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →