FDAClass IISeptember 18, 2013

Glutathione 100 mg/mL Injectable recall: Contamination

Glutathione 100 mg/mL Injectable, 100mL Vial, Use as Directed, RX, Creative Compounds, Wilsonville, OR 97070.

Why was Glutathione 100 mg/mL Injectable recalled?

Glutathione 100 mg/mL injectable human drug is recalled due to Out Of Specification results or potential bacterial contamination and it was reported as passing by a contract laboratory.

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 #: 20130715@12, Exp10/13/2013

Product
Glutathione 100 mg/mL Injectable, 100mL Vial, Use as Directed, RX, Creative Compounds, Wilsonville, OR 97070.
Recalling firm
Creative Compounds
Quantity
16 vials
Distribution
Oregon and Washington
Recall date
September 18, 2013
Classification
Class II
Status
Terminated
Agency
FDA (drug)
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