FDA recall record

United Pharmacy Glutamine, Arginine and Carnitine, 10/100/200mg/mL, 30 mL (Multi Dose Vial) recall — FDA D-0008-2018

CGMP Deviations; FDA analysis deterrmined that the product does not contain glutamine and two unknown impurities were observed

Class IIclassification
D-0008-2018official record ID
Oct 18, 2017report date

Recall record at a glance

Official recordD-0008-2018
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmUnited Pharmacy
Report dateOct 18, 2017
Recall initiation dateSep 27, 2017
Quantity268 vials
LocationWest Palm Beach, FL, United States

Official product description

Glutamine, Arginine and Carnitine, 10/100/200mg/mL, 30 mL (Multi Dose Vial), Rx Only, For Injection, United Pharmacy Compounded, 13951 N. Haverhill Rd Ste. 120-121 West Palm Beach, FL 33417

Why the product was recalled

CGMP Deviations; FDA analysis deterrmined that the product does not contain glutamine and two unknown impurities were observed

Distribution information

Nationwide.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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