PlainRecalls
FDA Drug Moderate Class II Terminated

Hydromorphone HCl 1 mg/mL in 0.9% Sodium Chloride, injectable packed in syringes, Total dosage 1 mg/ 1mL, Rx only, PHARMAKON Pharmaceuticals, Inc.

Reported: February 3, 2016 Initiated: August 19, 2015 #D-0598-2016

Product Description

Hydromorphone HCl 1 mg/mL in 0.9% Sodium Chloride, injectable packed in syringes, Total dosage 1 mg/ 1mL, Rx only, PHARMAKON Pharmaceuticals, Inc.

Reason for Recall

Stability data does not support expiry.

Details

Recalling Firm
Pharmakon Pharmaceuticals
Units Affected
8000
Distribution
Nationwide
Location
Noblesville, IN

Frequently Asked Questions

What product was recalled?
Hydromorphone HCl 1 mg/mL in 0.9% Sodium Chloride, injectable packed in syringes, Total dosage 1 mg/ 1mL, Rx only, PHARMAKON Pharmaceuticals, Inc.. Recalled by Pharmakon Pharmaceuticals. Units affected: 8000.
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-0598-2016.