Dr. Reddy's recalls extended-release allergy and congestion tablets due to failed dissolution specifications. Consumers should check NDC 0536-1242-34 and lot number AC2103329H for affected products.
Failed dissolution specifications
Dr. Reddy's is recalling allergy and congestion tablets that may not dissolve properly. This could lead to inconsistent medication delivery and potential health risks if the tablets don't release the active ingredients as intended.
The tablets may not dissolve properly in the body, leading to inconsistent release of the active ingredients. This could cause the medication to not work as intended or cause unexpected side effects.
People who purchased the specific allergy and congestion tablets with NDC 0536-1242-34 and lot number AC2103329H from Rugby Laboratories are affected. Those with allergies or congestion symptoms are most at risk from inconsistent medication delivery.
Check for the NDC code 0536-1242-34 and lot number AC2103329H on the product packaging. These tablets were distributed by Rugby Laboratories and sold between the manufacturing date and expiration of January 2023.
Look for the NDC code 0536-1242-34 and lot number AC2103329H on the product packaging to confirm if it's affected.
The product was recalled because it failed dissolution specifications, meaning the tablets may not dissolve properly in the body.
Check the product packaging for the NDC code 0536-1242-34 and lot number AC2103329H. If it matches, contact Rugby Laboratories for instructions.
The recall is for inconsistent medication delivery, not a risk of serious injury. The danger level is low risk.
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-0270-2022 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0270-2022 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.
