PlainRecalls
FDA Drug Moderate Class II Terminated

Potassium Chloride Oral Solution, USP, 10%, 20 mEq per 15 mL, packaged in 15 mL unit dose cups (NDC 66689-047-01), 50 unit dose cups per case (NDC 66689-047-50), Rx only, Xact Dose, Manufactured by VistaPharm, Largo, FL 33771.

Reported: February 15, 2017 Initiated: January 18, 2017 #D-0469-2017

Product Description

Potassium Chloride Oral Solution, USP, 10%, 20 mEq per 15 mL, packaged in 15 mL unit dose cups (NDC 66689-047-01), 50 unit dose cups per case (NDC 66689-047-50), Rx only, Xact Dose, Manufactured by VistaPharm, Largo, FL 33771.

Reason for Recall

Defective Container: Leakage of unit dose cups that may occur at the seal.

Details

Recalling Firm
VistaPharm, Inc.
Units Affected
13,609 cases
Distribution
Domestic: AL, AZ, CA, CO, CT, FL, GA, HI, IA, IL, IN, KS, KY, LA, MA, MI, MN, MO, MS, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA WI, & WV.
Location
Largo, FL

Frequently Asked Questions

What product was recalled?
Potassium Chloride Oral Solution, USP, 10%, 20 mEq per 15 mL, packaged in 15 mL unit dose cups (NDC 66689-047-01), 50 unit dose cups per case (NDC 66689-047-50), Rx only, Xact Dose, Manufactured by VistaPharm, Largo, FL 33771.. Recalled by VistaPharm, Inc.. Units affected: 13,609 cases.
Why was this product recalled?
Defective Container: Leakage of unit dose cups that may occur at the seal.
Which agency issued this recall?
This recall was issued by the FDA Drug on February 15, 2017. Severity: Moderate. Recall number: D-0469-2017.