FDA Drug Recalls

Recalls / Class II

Class IID-1158-2018

Product

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

Affected lot / code info
Lot #: 180529/2, Exp 27-Aug-18 and 180620/11, Exp 18-Sep-18

Why it was recalled

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

Recalling firm

Firm
Auro Pharmacies, Inc.
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
520 W La Habra Blvd, N/A, La Habra, California 90631-5308

Distribution

Quantity
91 vials
Distribution pattern
Nationwide in USA

Timeline

Recall initiated
2018-08-21
FDA classified
2018-08-29
Posted by FDA
2018-09-05
Terminated
2020-01-30
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1158-2018. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls