FDA · Drugs ·
Ketamine Hydrochloride Injectable Solution recall
Wells Pharma of Houston LLC recalled Ketamine Hydrochloride Injectable Solution on May 6, 2026 because of cGMP deviations. It was sold nationwide.
Why it was recalled
cGMP deviations.
What's recalled
Ketamine Hydrochloride Injectable Solution, 50mg/ml, (50 mg per mL) Volume: 1 mL, 5265 Kitty Drive, Houston, TX 77054, NDC 73702-302-31.
Quantity: 4975 syringes
What to do
Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.
Read the official FDA noticeDetails
- Company
- Wells Pharma of Houston LLC, Houston, TX
- Date
- Severity
- Class II
the product could cause temporary or reversible health problems. - Where sold
- Nationwide
U.S. Nationwide. - Status
- Ongoing
- Recall number
- D-0507-2026
- Source
- U.S. Food and Drug Administration
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