InvaTech Pharma Solutions, LLC recalls Levocetirizine Dihydrochloride Tablets, USP, 5 mg 30-count bottle, Rx Only, Distributed by: Marlex Pharmceuticals, Inc.
InvaTech Pharma Solutions recalls 5mg Levocetirizine tablets that failed stability testing. Affected lots may degrade, causing potential safety issues. Contact for details.
Lower-risk recall
Failed Impurities/Degradation Specifications: One lot of Levocetirizine dihydrochloride tablets 5 mg 30 count failed stability testing.
Contact the company & request your remedy
What happened, in plain English
InvaTech Pharma Solutions is recalling 5 mg Levocetirizine Dihydrochloride Tablets that failed stability testing. This means the tablets could degrade over time, potentially causing safety risks for users. Read more at govinfonow.com/recall/36686-invatech-levocetirizine-tablets-recall-failed-stability-testing.
Source Summary by GovInfoNow · govinfonow.com/recall/36686-invatech-levocetirizine-tablets-recall-failed-stability-testing · Updated October 4, 2026 · FDA enforcement record: FDA #D-0115-2021
Cite this page
“InvaTech Levocetirizine Tablets Recall: Failed Stability Testing.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36686-invatech-levocetirizine-tablets-recall-failed-stability-testing. Based on FDA recall #D-0115-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0115-2021%22&limit=1).
Why it’s dangerous
The tablets failed stability testing, meaning they may degrade over time. This degradation could lead to potential safety issues, though the exact risk is not specified in the recall.
Who’s affected
People with a prescription for 5 mg Levocetirizine tablets from InvaTech Pharma Solutions. Those who have the specific lot numbers listed in the recall are most at risk.
How to tell if you have this one
Check for the product name 'Levocetirizine Dihydrochloride Tablets, USP, 5 mg 30-count bottle' with the lot numbers 051944A (exp. April 2021), 1119124 (exp. Oct 2021), or 062088 (exp. June 2022).
- Brand
InvaTech Pharma Solutions- Category
Drug
What to do — step by step
Check Product Details
Look for the lot numbers 051944A, 1119124, or 062088 on the packaging to confirm if your tablets are affected.
Questions people ask
Why is this product being recalled?
The tablets failed stability testing, which means they may degrade over time and pose potential safety risks.
What should I do if I have these tablets?
Check the lot number on your packaging. If it matches 051944A, 1119124, or 062088, contact InvaTech Pharma Solutions for further instructions.
Are there any safety risks from using these tablets?
The recall states the tablets may degrade, but the exact risk is not specified. Consult your healthcare provider for advice.
Contact InvaTech Pharma Solutions
We’ve drafted a message you can send InvaTech Pharma Solutions to request your refund or repair — edit it as you like.
Subject: Recall D-0115-2021 — InvaTech Pharma Solutions InvaTech Pharma Solutions Hello, I own a InvaTech Pharma Solutions that is covered by recall D-0115-2021 from InvaTech Pharma Solutions. 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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Where this comes from
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.
- Official source: FDA Recall #D-0115-2021 (November 11, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0115-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.