FDA recall D-0057-2017

Pharmedium Services, LLC · Class II · drug

Product

ketamine HCl Injection, 50 mg per mL (100 mg per 2 mL), 2 mL Total Volume in a syringe, Rx only, PharMEDium, For IV Use, Product code 2R3500.

Reason for recall

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

Distribution

Nationwide

Key facts

Status
Terminated
Initiation date
2015-07-17
Report date
2016-10-19
Termination date
2017-06-23
Voluntary/Mandated
Voluntary: Firm initiated
Location
Lake Forest, IL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0057-2017