Dr. Reddy's recalls 20-count allergy and congestion tablets with failed dissolution specifications. This may affect medication effectiveness. Contact Rite Aid for details.
Failed dissolution specifications
Dr. Reddy's recalls allergy and congestion tablets that may not dissolve properly, potentially reducing medication effectiveness. This recall affects specific lots distributed by Rite Aid.
The tablets failed to dissolve properly as specified, which could lead to reduced medication effectiveness. This means the treatment might not work as intended for allergy and congestion symptoms.
People who purchased the 20-count allergy and congestion tablets with the specific lot number AC2103329E from Rite Aid. Those with allergies or congestion symptoms are most at risk.
Check for the product name 'Allergy & Congestion Fexofenadine HCl 60 mg & Pseudoephedrine HCl 120 mg Extended-Release Tablets, USP, 20'. Look for the lot number AC2103329E on the packaging.
Identify the lot number AC2103329E on the packaging to confirm if your tablets are affected.
The affected lot number is AC2103329E.
Contact Rite Aid at 30 Hunter Lane, Camp Hill, PA 17011 for details.
The recall record does not specify a remedy.
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-0267-2022 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0267-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
