Wells Pharma recalls phenylephrine hydrochloride injectable solution (40mg, 250mL) manufactured with cGMP deviations. Affected units have specific NDC and expiration dates listed in the recall notice.
cGMP deviations.
Wells Pharma is recalling phenylephrine hydrochloride injectable solution (40mg, 250mL) because of cGMP deviations. This means the product may not meet quality standards and could be unsafe for medical use.
cGMP deviations refer to failures in manufacturing quality control processes. This could result in the product not meeting safety and efficacy standards, potentially causing harm if used improperly.
Patients who have received this injectable solution from Wells Pharma of Houston LLC are affected. Healthcare providers using this product for medical treatments are at risk.
Check for the product name 'Phenylephrine Hydrochloride Injectable Solution, 40mg, 250mL Bag' with Wells Pharma of Houston LLC. The NDC code is 73702-122-03. Affected units have specific expiration dates listed in the recall notice.
Identify the product by checking the NDC code (73702-122-03) and expiration date on the packaging.
The recall indicates cGMP deviations, which means the product may not meet quality standards. It is not safe to use without confirming it is not recalled.
The recall does not specify a remedy, so contact Wells Pharma directly for guidance on handling the product.
Check the NDC code (73702-122-03) and expiration date on the packaging. Affected units are listed in the recall notice with specific expiration dates.
We’ve drafted a message you can send Wells Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0502-2026 — Wells Pharma Wells Pharma Hello, I own a Wells Pharma that is covered by recall D-0502-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.