FDAClass IIIFebruary 15, 2017

Pantoprazole Sodium for Injection recall

Pantoprazole Sodium for Injection, 40mg per vial, Single-dose vial, Rx only, Mfd. in India for: Auromedics Pharma LLC 6 Wheeling Road, Dayton, NJ…

Why was Pantoprazole Sodium for Injection recalled?

Discoloration: Some vials were found to contain powder with a yellowish-brownish appearance.

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Lot #: CPO160028, Exp. June 2018

Product
Pantoprazole Sodium for Injection, 40mg per vial, Single-dose vial, Rx only, Mfd. in India for: Auromedics Pharma LLC 6 Wheeling Road, Dayton, NJ…
Recalling firm
Aurobindo Pharma USA Inc
Quantity
29800 vials
Distribution
Nationwide in US
Recall date
February 15, 2017
Classification
Class III
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls