Dr. Reddy's recalls allergy and congestion tablets with potential dissolution failure. Consumers should check lot numbers and expiration dates for affected batches.
Failed Dissolution Specifications
Dr. Reddy's recalls specific allergy and congestion tablets that may not dissolve properly. This could lead to inconsistent medication delivery and potential health risks if the medication doesn't work as intended.
The tablets may not dissolve correctly in the body, leading to inconsistent medication release. This could cause the medication to not work as intended, potentially affecting symptom relief for allergies and congestion.
People who purchased the Rite Aid Pharmacy allergy and congestion tablets with the specified lot numbers and expiration dates are affected. Those with allergies to fexofenadine or pseudoephedrine should avoid these products.
Check the box for the product name 'Allergy & Congestion, Fexofenadine HCl 60mg & Pseudoephedrine HCl 120mg, Extended Release Tablets'. Look for lot numbers AC2103330D (expiring 1/31/2023) or AC2106452E (expiring 3/31/2023).
Identify the lot number and expiration date on the packaging to determine if your product is affected.
The recalled product is Rite Aid Pharmacy Allergy & Congestion, Fexofenadine HCl 60mg & Pseudoephedrine HCl 120mg, Extended Release Tablets with lot numbers AC2103330D (expiring 1/31/2023) or AC2106452E (expiring 3/31/2023).
The recall record does not specify a remedy.
Check the lot number and expiration date on the packaging. Affected products have lot numbers AC2103330D (expiring 1/31/2023) or AC2106452E (expiring 3/31/2023).
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-0380-2022 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0380-2022 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.
