PlainRecalls
FDA Drug Moderate Class II Terminated

ketamine HCl, 10 mg per mL, 50 mg per 5 mL, in 0.9% Sodium Chloride, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3234.

Reported: October 19, 2016 Initiated: July 17, 2015 #D-0053-2017

Product Description

ketamine HCl, 10 mg per mL, 50 mg per 5 mL, in 0.9% Sodium Chloride, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3234.

Reason for Recall

Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.

Details

Recalling Firm
Pharmedium Services, LLC
Units Affected
25 syringes
Distribution
Nationwide
Location
Lake Forest, IL

Frequently Asked Questions

What product was recalled?
ketamine HCl, 10 mg per mL, 50 mg per 5 mL, in 0.9% Sodium Chloride, 5 mL Total Volume in a syringe, For IV Use, Rx only, PharMEDium, Product code 2R3234.. Recalled by Pharmedium Services, LLC. Units affected: 25 syringes.
Why was this product recalled?
Stability Data Does Not Support Expiry: potential loss of potency in drugs packaged and stored in syringes.
Which agency issued this recall?
This recall was issued by the FDA Drug on October 19, 2016. Severity: Moderate. Recall number: D-0053-2017.