FDAClass IIJuly 20, 2016

Phenylephrine HCI 40mg/250 mL in 0.9% Sodium Chloride recall: Sterility Concern

Phenylephrine HCI 40mg/250 mL in 0.9% Sodium Chloride 250 mL bag, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC…

Why was Phenylephrine HCI 40mg/250 mL in 0.9% Sodium Chloride recalled?

Lack of Assurance of Sterility

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?

All Sterile Compounded Products within Expiry

Product
Phenylephrine HCI 40mg/250 mL in 0.9% Sodium Chloride 250 mL bag, Rx Only, Compounded by PHARMAKON Pharmaceuticals, Noblesville, IN 46060, NDC…
Recalling firm
Pharmakon Pharmaceuticals, Inc.
Quantity
10
Distribution
Nationwide VA/DOD: CA, KY, MD, NC, OK, TX, VA
Recall date
July 20, 2016
Classification
Class II
Status
Terminated
Agency
FDA (drug)
Open FDA enforcement record Latest recalls