FDA recall record

RXQ Compounding methylPREDNIsolone ACETATE, 40 MG/ML INJECTION SUSPENSION, 10 ML Vial, RXQ recall — FDA D-0012-2018

Lack of Assurance of Sterility; autoclave parameters were not correct for one of two autoclaves used to sterilize the product.

Class IIclassification
D-0012-2018official record ID
Oct 25, 2017report date

Recall record at a glance

Official recordD-0012-2018
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmRXQ Compounding LLC
Report dateOct 25, 2017
Recall initiation dateSep 25, 2017
Quantity945 vials
LocationAthens, OH, United States

Official product description

methylPREDNIsolone ACETATE, 40 MG/ML INJECTION SUSPENSION, 10 ML Vial, RXQ Compounding, Athens, OH --- NDC: 70731-0936-10

Why the product was recalled

Lack of Assurance of Sterility; autoclave parameters were not correct for one of two autoclaves used to sterilize the product.

Distribution information

TX, LA, PA, MA, FL, and OH

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: Telephone.

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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