Seaway Pharma recalls Premier Value Tussin Cough DM due to possible microbial contamination in the water used during manufacturing. No contamination was found in the final products. Consumers should check their bottles for lot number SD23033.
CGMP Deviations: Firm reported possible microbial contamination in the purified water used in the manufacturing of the products. No contamination was found in the final products.
Seaway Pharma is recalling Premier Value Tussin Cough DM products because of possible microbial contamination in the water used during manufacturing. This recall does not indicate contamination in the final products, so the risk is low.
The recall is based on possible microbial contamination in the purified water used during manufacturing. However, no contamination was found in the final products, so the risk to consumers is minimal.
People who own or use Premier Value Tussin Cough DM products with lot number SD23033 are affected. Children and elderly individuals may be at slightly higher risk due to potential sensitivity to medication.
Check the bottle for the lot number SD23033. The product is an 8 fl oz (237 mL) bottle distributed by Pharmacy Value Alliance, LLC.
Look for the lot number SD23033 on the bottle label.
The recall states no contamination was found in the final products, so the product is safe to use if it has the correct lot number.
Check the lot number on the bottle. If it is SD23033, you do not need to take any action as the product is safe.
The recall indicates no contamination in the final products, so there is no risk of serious injury.
We’ve drafted a message you can send Seaway Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0215-2024 — Seaway Pharma Seaway Pharma Hello, I own a Seaway Pharma that is covered by recall D-0215-2024 from Seaway 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.
