Dr. Reddy's recalls certain fexofenadine and pseudoephedrine extended-release tablets due to failed dissolution specifications. Affected lots and UPCs are listed; consumers should contact the manufacturer for details.
Failed Dissolution Specifications
Dr. Reddy's is recalling specific batches of fexofenadine and pseudoephedrine extended-release tablets because they failed dissolution tests. This could mean the medication doesn't work as intended, but the recall does not indicate immediate safety risks.
The tablets failed dissolution specifications, meaning they may not release the medication properly in the body. This could lead to ineffective treatment, but the recall does not indicate a risk of injury or harm to users.
People who own or use the recalled tablets, particularly those with allergies to fexofenadine or pseudoephedrine. Those with specific medical conditions requiring these medications may be most affected.
Check for the following: 10-count boxes with UPC 343598823355, 20-count boxes with UPC 343598823140, or 30-count boxes with UPC 343598823317. Also check the lot numbers and expiration dates listed.
Identify the box UPC code and lot number to confirm if your tablets are affected.
The recall is due to failed dissolution specifications, which may affect effectiveness but does not indicate immediate safety risks.
Check the UPC codes: 343598823355 (10-count), 343598823140 (20-count), or 343598823317 (30-count). Also check the lot numbers and expiration dates.
The recall does not specify a remedy, so contact Dr. Reddy's Laboratories, Inc. for further instructions.
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-0382-2022 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0382-2022 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.
