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Medium risk Drugs & MedicationsClass II

Wells Pharma Ketamine Injectable Recall

Ketamine Hydrochloride Injectable Solution, 50mg/ml, (50 mg per mL) Volume: 1 mL, 5265 Kitty Drive, Houston, TX 77054, NDC 73702-302-31.

Updated April 1, 2026

Ketamine Hydrochloride Injectable Solution 50 mg/mL manufactured by Wells Pharma of Houston has been recalled due to manufacturing quality deviations. Stop using this product and contact your healthcare provider or pharmacist immediately.

Is the Wells Pharma of Houston LLC recalled? Yes. This product was recalled by FDA on April 1, 2026. Details below.

What is recalled

Ketamine Hydrochloride Injectable Solution, 50 mg/mL, 1 mL vials, NDC 73702-302-31, manufactured by Wells Pharma of Houston LLC, 5265 Kitty Drive, Houston, TX 77054.

Am I affected

You're affected if you have a Ketamine Hydrochloride Injectable Solution vial with NDC number 73702-302-31 on the label and a concentration of 50 mg/mL.

What to do right now

Stop using this product immediately. Contact your healthcare provider or pharmacist right away if you have received this medication. Do not use it for any purpose.

The hazard

CGMP deviations.

Brands affected

Wells Pharma of Houston LLC
Source
FDA
Category
Drugs & Medications
Recall ID
fda-D-0507-2026
Classification
Class II
Recalled
April 1, 2026
Read the official notice

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