Exact FDA event identifier

Event 89923

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

Event summary

Timeline bucket: April 01, 2022
Product types: Drug
Classifications: Class III
Statuses: Terminated
Recalling firm wording: Jubilant Cadista Pharmaceuticals, 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

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

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

Methylprednisolone Tablets, USP 4mg, 100-count bottle, Rx Only, Manufactured by: Jubliant Cadista Pharmaceuticals Inc. Salisbury, MD 21801, USA, NDC 59746-001-06

D-0752-2022

Recall number: D-0752-2022
Initiated: April 01, 2022
Classification: Class III
Status: Terminated
Recalling firm: Jubilant Cadista Pharmaceuticals, Inc.
Quantity: 19,222 Bottles (100-count)

App-derived interpretation

Potency or specification failure reason.potency_specification_failure · v1.0.0

Subpotent

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Subpotent

Code information

Lot # 21 P0322, Exp. 01/2023

Distribution pattern

Nationwide in the USA and Puerto Rico