Dr. Reddy's Leader allergy and congestion relief tablets with failed dissolution specifications are being recalled. This may affect safety and effectiveness of the medication.
Failed Dissolution Specifications
Dr. Reddy's Leader allergy and congestion relief tablets are being recalled because they failed to dissolve properly as tested. This could lead to inconsistent medication delivery and potential safety issues.
The medication failed to dissolve properly during testing, which could mean inconsistent dosing. This might lead to ineffective treatment for allergies or congestion symptoms.
People who own or use the recalled Leader allergy and congestion relief tablets. Those with allergies or congestion symptoms may be at higher risk if the medication doesn't work as intended.
Check for the product name 'Leader, 12HR Allergy & Congestion Relief' with 20 extended release tablets per box. The NDC code is 70000-0518-1. Lot numbers include 79C002625B (expiring 4/30/2022), AC2103328G (expiring 1/31/2023), and AC2106452C (expiring 3/31/2023).
Look for the product name, NDC code, and lot numbers listed in the recall notice to confirm if your tablets are affected.
The medication failed to dissolve properly as tested, which could lead to inconsistent dosing and potential safety issues.
The recall notice does not specify a remedy, so check the product details to confirm if your tablets are affected and contact Dr. Reddy's for further instructions.
Check for the product name 'Leader, 12HR Allergy & Congestion Relief' with 20 extended release tablets per box, NDC 70000-0518-1, and lot numbers 79C002625B (expiring 4/30/2022), AC2103328G (expiring 1/31/2023), or AC2106452C (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-0386-2022 — Dr. Reddy's Dr. Reddy's Hello, I own a Dr. Reddy's that is covered by recall D-0386-2022 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.
