FDA recall record

Auro Pharmacies Dexpanthenol injectable, 250 mg/mL, 10 mL Single Dose vial recall — FDA D-1158-2018

Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.

Class IIclassification
D-1158-2018official record ID
Sep 5, 2018report date

Recall record at a glance

Official recordD-1158-2018
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmAuro Pharmacies, Inc.
Report dateSep 5, 2018
Recall initiation dateAug 21, 2018
Quantity91 vials
LocationLa Habra, CA, United States

Official product description

Dexpanthenol injectable, 250 mg/mL, 10 mL Single Dose vial, Rx only, Central Drugs Compounding Pharmacy, 520 W. La Habra Blvd, La Habra, CA 90631

Why the product was recalled

Lack of Assurance of Sterility: Inadequate processes and equipment to assure the sterility of products intended to be sterile.

Distribution information

Nationwide in USA

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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