A-S Medication Solutions recalls 10mg cetirizine tablets due to incorrect labeling showing 90 tablets when only 30 were actually in the box. This may cause confusion about dosage.
Labeling: Not Elsewhere classified: Product was relabeled as 90 tablet count product although it was a manufacturer in a box with 30 tablet count tablets.
Take action
Contact the company
📍Recalling firmA-S Medication Solutions LLC.2401 Commerce Dr · Libertyville, IL 60048-4464
✎ GovInfoNow plain-language explainer
A-S Medication Solutions is recalling 10mg cetirizine hydrochloride tablets that were labeled as 90-count but actually contain only 30 tablets. This labeling error could lead to incorrect dosing if users assume there are more tablets than actually present. Read more at govinfonow.com/recall/35805-a-s-medication-solutions-recalls-10mg-cetir-labeling-error-in.
“A-S Medication Solutions recalls 10mg Cetir: Labeling error in 90-count bottle.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/35805-a-s-medication-solutions-recalls-10mg-cetir-labeling-error-in. Based on FDA recall #D-0096-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0096-2022%22&limit=1).
The FDA announced on 2021-10-05 that A-S Medication Solutions LLC voluntarily recalled Cetirizine hydrochloride, 10 mg tablets in 90-count bottles due to labeling errors. The product was relabeled as containing 90 tablets when it actually contained 30. Owners should contact the company for a refund.
The product was relabeled as a 90 tablet count product although it was a manufacturer in a box with 30 tablet count tablets. This labeling error constitutes the hazard.
Context
GovInfoNow's records show A-S Medication Solutions LLC has had 5 other recalls on record since 2016-04-22. Recent recalls include a 2025-02-25 recall of Metformin Extended-Release Tablets due to foreign tablets, a 2024-06-21 recall where Acetaminophen was labeled as Aspirin, and a 2021-03-02 Health Essentials Kit Acetaminophen label mix-up. Other recent recalls of similar products include an American Regent Levocarnitine Injection recall (2026-04-16), a Meclizine 12.5mg Tablets recall (2026-03-16), and an American Health Packaging Buprenorphine Tablets recall (2026-08-19).
How to tell if you have this one
Check for the 10mg cetirizine hydrochloride tablets in a 90-count bottle with the manufacturer's address in Libertyville, IL. The product was distributed by A-S Medication Solutions with NDC code 50090-5510-3.
Brand
A-S Medication Solutions
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Label
Verify the product label shows 90 tablets, but the actual contents contain only 30 tablets.
Where it went and when
Where it was distributed
Distributed in 4 states.
Listed by the agency
Not listed
FDA distribution: “FL, IN, MN, WI” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida, Indiana, Minnesota, Wisconsin.
Recall timeline
FDA terminated this recall 10 months after the firm started it.
1Firm started the recall
2FDA classified it Class III
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The recall does not require immediate action, but you should check the label to confirm the tablet count and contact the manufacturer if you have concerns.
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-0096-2022 (October 5, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0096-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.