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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 95999

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

Open FDA event record

Event summary

Timeline bucket
December 19, 2024
Product types
Drug
Classifications
Class III
Statuses
Ongoing
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

Methadone Hydrochloride Tablets, USP, 5mg, 10x10 Unit-Dose Tablets, Rx Only, Distributed by: Hikma Pharmaceuticals USA Inc., Berkeley Heights, NJ 07922, NDC 0054-0709-20

D-0183-2025
Recall number
D-0183-2025
Initiated
December 19, 2024
Classification
Class III
Status
Ongoing
Recalling firm
West-Ward Columbus Inc
Quantity
2591 100-count boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Failed Tablet/Capsule Specifications: Illegible product identification for the unit dose configuration only.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Tablet/Capsule Specifications: Illegible product identification for the unit dose configuration only.

Code information

Lot # AC2556A; Exp. 03/2027

Distribution pattern

US Nationwide.