PlainRecalls
LowClass IIITerminated

FDA Drug recall · Reported August 19, 2020

Leucovorin Calcium Tablets USP, 10 mg, Rx only, 24 Tablets per bottle, Distr. by: West-Ward Pharmaceuticals Corp. Eatontown, NJ 07724, NDC 0054-4497-10

Failed Tablet/Capsule Specifications: Tablets are imprinted with the incorrect identification code.

Recall #
D-1490-2020
Affected scope
2300 bottles
Initiated
July 22, 2020
Compiled from official public sources by the editorial team.
Verify with FDA Drug →
View my saved recalls

West-Ward Columbus Inc recalled Leucovorin Calcium Tablets USP, 10 mg, Rx only, 24 Tablets per bottle, Distr. by: West-Wa… - a low-severity action.

Leucovorin Calcium Tablets USP, 10 mg, Rx only, 24 Tablets per bottle, Distr. by: West-Wa… was recalled by West-Ward Columbus Inc in August 19, 2020. Reason: Failed Tablet/Capsule Specifications: Tablets are imprinted with the incorrect identification code.. Check the official notice for the remedy. Verify recall #D-1490-2020 with the FDA Drug before acting.

The recall

West-Ward Columbus Inc issued this low-severity FDA Drug recall-Failed Tablet/Capsule Specifications: Tablets are imprinted with the incorrect identification code..

Low
severity level
Class III
classification
August 19, 2020
reported

Sourced from official FDA Drug enforcement records. Verify recall #D-1490-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Drug action (record #D-1490-2020) was formally reported on August 19, 2020, with the manufacturer initiating the action on July 22, 2020. It is classified under Low severity (Class III), with a current status of Terminated. West-Ward Columbus Inc is listed as the recalling firm, operating out of Columbus, OH. Federal records list the affected scope as 2300 bottles.

The documented reason for this recall is: Failed Tablet/Capsule Specifications: Tablets are imprinted with the incorrect identification code. Distribution data in the federal record shows the product reached: OH and MS. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 5 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Drugs & Medications recalls over time

Where this recall sits in its category - 14,287 drugs & medications recalls on record

-50005001,0001,5002,000 2006201220152018202120242026 263
Severity2487872426High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Severity

Low

Affected scope

2300 bottles

Related Recalls

6

5 from same agency

Product description

Leucovorin Calcium Tablets USP, 10 mg, Rx only, 24 Tablets per bottle, Distr. by: West-Ward Pharmaceuticals Corp. Eatontown, NJ 07724, NDC 0054-4497-10

Reason for recall

Failed Tablet/Capsule Specifications: Tablets are imprinted with the incorrect identification code.

Recall Profile

Structured summary of the FDA Drug recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Low (Class III)
Status Terminated
Recall number D-1490-2020
Date reported August 19, 2020
Date initiated July 22, 2020
Recalling firm West-Ward Columbus Inc
Firm location Columbus, OH
Affected scope 2300 bottles
Distribution OH and MS

Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (D-1490-2020) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Drug before acting, recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
Leucovorin Calcium Tablets USP, 10 mg, Rx only, 24 Tablets per bottle, Distr. by: West-Ward Pharmaceuticals Corp. Eatontown, NJ 07724, NDC 0054-4497-10. Recalled by West-Ward Columbus Inc. Units affected: 2300 bottles.
Why was this product recalled?
Failed Tablet/Capsule Specifications: Tablets are imprinted with the incorrect identification code.
Which agency issued this recall?
This recall was issued by the FDA Drug on August 19, 2020. Severity: Low. Recall number: D-1490-2020.
Where was the recalled product distributed?
Distribution: OH and MS.
How do I check if my product is affected by a recall?
Check the product description and recall number (D-1490-2020) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device?
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

Nearby Recalls in This Category

Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.

Compare this recall with PRED MILD, prednisolone acetate ophthalmic suspension, USP,… →

Browse all Drugs & Medications recalls →

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported August 19, 2020. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.