PlainRecalls
FDA Drug Moderate Class II Terminated

Phenylephrine (PF) 100 mcg/mL in 0.9% Sodium Chloride, injectable packed in syringes, Total dosage 500 mcg/ 5mL, Rx only, PHARMAKON Pharmaceuticals, Inc.

Reported: February 3, 2016 Initiated: August 19, 2015 #D-0590-2016

Product Description

Phenylephrine (PF) 100 mcg/mL in 0.9% Sodium Chloride, injectable packed in syringes, Total dosage 500 mcg/ 5mL, Rx only, PHARMAKON Pharmaceuticals, Inc.

Reason for Recall

Stability data does not support expiry.

Details

Recalling Firm
Pharmakon Pharmaceuticals
Units Affected
N/A
Distribution
Nationwide
Location
Noblesville, IN

Frequently Asked Questions

What product was recalled?
Phenylephrine (PF) 100 mcg/mL in 0.9% Sodium Chloride, injectable packed in syringes, Total dosage 500 mcg/ 5mL, Rx only, PHARMAKON Pharmaceuticals, Inc.. Recalled by Pharmakon Pharmaceuticals. Units affected: N/A.
Why was this product recalled?
Stability data does not support expiry.
Which agency issued this recall?
This recall was issued by the FDA Drug on February 3, 2016. Severity: Moderate. Recall number: D-0590-2016.