Failed Tablet/Capsule Specifications: Tablets are imprinted with the incorrect identification code.
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📍Recalling firmWest-Ward Columbus Inc1809 Wilson Rd · Columbus, OH 43228-9579
✎ GovInfoNow plain-language explainer
West-Ward Columbus Inc is recalling one lot of Leucovorin Calcium Tablets USP, 10 mg because the tablets are imprinted with the wrong identification code. This affects 2,300 bottles distributed in Ohio and Mississippi. The company has not yet provided a remedy or return instructions for this recall. Read more at govinfonow.com/recall/36919-west-ward-recalls-leucovorin-calcium-tablets-due-to-labeling-error.
“West-Ward Recalls Leucovorin Calcium Tablets Due to Labeling Error.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/36919-west-ward-recalls-leucovorin-calcium-tablets-due-to-labeling-error. Based on FDA recall #D-1490-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1490-2020%22&limit=1).
West-Ward Columbus Inc recalled Leucovorin Calcium Tablets USP, 10 mg, distributed by West-Ward Pharmaceuticals Corp., because tablets bear an incorrect identification code, the FDA said on July 22, 2020. The recall involves 2,300 bottles distributed in Ohio and Mississippi.
How to tell if you have it
Brand: West-Ward
Product: Leucovorin Calcium Tablets USP, 10 mg
NDC: 0054-4497-10
Lot: #064046A
Expiration Date: 03/2022
Quantity: 24 Tablets per bottle
Distribution: Ohio and Mississippi
The hazard
The tablets are imprinted with the incorrect identification code, failing tablet specifications. The FDA classified this as a Class III recall.
Context
GovInfoNow's records show West-Ward Columbus Inc has issued eight other recalls since May 19, 2016. Recent West-Ward recalls include methadone tablets with illegible labels on Dec. 19, 2024, and methotrexate tablets with unsmooth surfaces and illegible labels on Sept. 22, 2023. Other recent recalls of similar products include Unichem's doxazosin tablets recall due to wrong ID imprint (Jan. 21, 2026), American Regent's levocarnitine injection recall for missing labels (April 16, 2026), and American Health Packaging's buprenorphine tablets recall for label mix-ups (Aug. 19, 2026).
How to tell if you have this one
Check your bottle for NDC 0054-4497-10 and Lot #064046A with an expiration date of 03/2022. The product is Leucovorin Calcium Tablets USP, 10 mg, Rx only, containing 24 tablets per bottle.
Brand
West-Ward
Category
Drug
Based on the official FDA remedy
What to do — step by step
Check Your Medication
Verify if your Leucovorin Calcium Tablets match NDC 0054-4497-10 and Lot #064046A expiring in 03/2022.
Contact Your Pharmacist
Speak with your pharmacist or healthcare provider to determine if you have the recalled product and what steps to take next.
Where it went and when
Where it was distributed
Distributed in Mississippi and Ohio.
Listed by the agency
Not listed
FDA distribution: “OH and MS” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Mississippi, Ohio.
Recall timeline
FDA terminated this recall 2.1 years 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 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-1490-2020 (July 22, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1490-2020 to see it in context.
Plain-language summary written by qwen3.6:35b-a3b on October 11, 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.