Dr. Reddy's Wal-Fex D extended-release tablets with failed dissolution specifications may not work as intended. Recall includes specific lot numbers and box sizes.
Failed Dissolution Specifications
Dr. Reddy's Wal-Fex D extended-release tablets are being recalled because they failed dissolution specifications. This means the medication may not release the active ingredients properly, potentially reducing effectiveness.
The tablets failed dissolution specifications, meaning they may not release the active ingredients at the correct rate. This could lead to reduced effectiveness of the medication, but does not pose a direct safety risk like injury or death.
People who purchased Wal-Fex D extended-release tablets with specific lot numbers and box sizes from Walgreen Co. in the US are affected. Those with allergies to fexofenadine or pseudoephedrine are at higher risk.
Check the box for 20 or 30 extended-release tablets with specific lot numbers listed in the recall notice. The product was distributed by Walgreen Co. in the US.
Identify the box size (20 or 30 tablets) and lot numbers from the recall notice to confirm if your product is affected.
The product failed dissolution specifications, meaning it may not release the active ingredients properly, potentially reducing effectiveness.
The recall does not specify a remedy, so check the product details to see if it is affected. If affected, contact Dr. Reddy's for further instructions.
The recall indicates a potential reduction in effectiveness, but there are no safety risks like injury or death.
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-0378-2022 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0378-2022 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.
