Apollo Care Ketamine Injection Recall: FDA Class II

Why it was recalled

Lack of Assurance of Sterility

Product description

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

Lot numbers, UPCs & expiration codes

Lot #: AC-016627, Exp. Date 06/17/2023; AC-016635, Exp. Date 07/08/2023; AC-016662, Exp. Date 09/30/2023

Where it was sold

Missouri only

What to do if you have this product

Compare the lot number and expiration date on your package with the codes above.
Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
If you have symptoms you think are related, contact your doctor. In an emergency call 911.
Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number: D-0635-2023
Classification: Class II
Status: Ongoing
Recall initiated: May 2, 2023
FDA report date: May 24, 2023
Quantity: 2040 syringes
Recall type: Voluntary: Firm initiated
Recalling firm: Apollo Care, LLC

Original FDA data

Every field from FDA enforcement report D-0635-2023, exactly as published.

Show all FDA fields

City: Columbia
State: MO
Status: Ongoing
Country: United States
Event ID: 92348
Address: 3801 Mojave Ct Ste 101
Code information: Lot #: AC-016627, Exp. Date 06/17/2023; AC-016635, Exp. Date 07/08/2023; AC-016662, Exp. Date 09/30/2023
Postal code: 65202-4042
Report date: May 24, 2023
Product type: Drugs
Recall number: D-0635-2023
Classification: Class II
Recalling firm: Apollo Care, LLC
Product quantity: 2040 syringes
Reason for recall: Lack of Assurance of Sterility
Voluntary / mandated: Voluntary: Firm initiated
Product description: 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
Distribution pattern: Missouri only
Recall initiation date: May 2, 2023
Initial firm notification: Letter
Center classification date: May 18, 2023

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0635-2023, published May 24, 2023. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

Apollo Care Ketamine Injection Recall

Summary