Dr. Reddy's recalls Allergy Relief D tablets that may not dissolve properly, potentially affecting medication effectiveness. This recall covers specific lot numbers and packaging sizes sold through Walmart.
Failed dissolution specifications
Dr. Reddy's recalls Allergy Relief D tablets that may not dissolve correctly, which could lead to improper medication delivery. This affects certain lot numbers sold through Walmart.
The tablets may not dissolve properly as intended, which could mean the medication isn't released correctly into the body. This might reduce effectiveness but does not pose a direct safety risk like injury or death.
People who own the specific lot numbers of Allergy Relief D tablets (NDC 49032-273-20 or 49032-273-30) sold through Walmart. Those with the listed expiration dates are most at risk.
Check for the product name 'Allergy Relief D' with the lot numbers AC2203133B (expiring 01/2024) or AC2203133A (expiring 01/2024). These were sold in 20-count or 30-count cartons through Walmart.
Look for the lot numbers AC2203133B or AC2203133A on the packaging to confirm if your tablets are affected.
Allergy Relief D tablets (Fexofenadine HCL 60mg/Antihistamine, Pseudoephedrine HCL 120mg/Nasal Decongestant, Extended-Release) with lot numbers AC2203133B or AC2203133A.
Check for the lot numbers AC2203133B (expiring 01/2024) or AC2203133A (expiring 01/2024) on the packaging, which were sold in 20-count or 30-count cartons through Walmart.
No, the recall is for potential reduced effectiveness, not a safety hazard. You can continue using them if they are not the affected lot numbers.
We’ve drafted a message you can send Dr. Reddy's to request your refund or repair — edit it as you like.
Subject: Recall D-0073-2023 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0073-2023 from Dr. Reddy's. 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.
