Wells Pharma recalls Ketamine Hydrochloride Injectable Solution due to cGMP deviations. This may affect safety and quality of the product. Check product details to see if you have the recalled batch.
cGMP deviations.
Wells Pharma is recalling a specific ketamine injectable solution product due to manufacturing quality control issues. This recall is important because it addresses potential safety risks from improper production standards.
The product was manufactured with cGMP (current Good Manufacturing Practice) deviations, which means the production process did not meet standard quality control requirements. This could lead to potential safety issues with the product's composition or effectiveness.
Patients who have received this ketamine injection product from Wells Pharma may be affected. Healthcare providers using this product for medical purposes are at risk.
Check the product label for the NDC code 73702-302-31 or the batch numbers listed in the recall notice. The product was sold with specific expiration dates between April 2026 and May 2026.
Review the product label for the NDC code 73702-302-31 or the batch numbers listed in the recall notice.
The recall notice states there were cGMP deviations, but does not specify if the product is safe to use. Wells Pharma has issued a recall, so it is recommended to check if you have the product and follow the action steps.
The recall notice does not provide a specific remedy, so you should check the product details and follow the action steps to determine if you need to take further action.
Check the product label for the NDC code 73702-302-31 or the batch numbers listed in the recall notice. The product was sold with specific expiration dates between April 2026 and May 2026.
We’ve drafted a message you can send Wells Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0507-2026 — Wells Pharma Wells Pharma Hello, I own a Wells Pharma that is covered by recall D-0507-2026 from Wells Pharma. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
