Apollo Care, LLC recalls Ketamine Injection, 50 mg per 5 mL (10 mg/mL), Single-Use Syringe, Rx only, Apollo Care, LLC, 3801 Mojave Ct., Suite 101
Recalled May 24, 2023 · FDA recall D-0635-2023 · Apollo Care
Hazard
Lack of Assurance of Sterility · FDA Class II
Units
2040 syringes
Sold at
Missouri only
Description
Lack of Assurance of Sterility
Product
Ketamine Injection, 50 mg per 5 mL (10 mg/mL), Single-Use Syringe, Rx only, Apollo Care, LLC, 3801 Mojave Ct., Suite 101, Columbia, MO 65202. NDC 71170-050-05
Manufacturer(s)
Apollo Care, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →