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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 86079

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
July 22, 2020
Product types
Drug
Classifications
Class III
Statuses
Terminated
Recalling firm wording
West-Ward Columbus Inc

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 1

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

D-1490-2020
Recall number
D-1490-2020
Initiated
July 22, 2020
Classification
Class III
Status
Terminated
Recalling firm
West-Ward Columbus Inc
Quantity
2300 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Failed Tablet/Capsule Specifications: Tablets are imprinted with the incorrect identification code.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

Lot: #064046A, Exp. 03/2022

Distribution pattern

OH and MS