Exact FDA event identifier

Event 95620

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

Event summary

Timeline bucket: October 29, 2024
Product types: Drug
Classifications: Class III
Statuses: Ongoing
Recalling firm wording: Dr. Reddy's Laboratories, 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

IBU (ibuprofen) 600 mg tablets, 500-count bottle, Rx Only, Distributor: Dr. Reddy's Laboratories Inc., Princeton, NJ 08540, Made in India, NDC 55111-683-05

D-0047-2025

Recall number: D-0047-2025
Initiated: October 29, 2024
Classification: Class III
Status: Ongoing
Recalling firm: Dr. Reddy's Laboratories, Inc.
Quantity: 3416 botttles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Failed Tablet/Capsule Specifications

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Failed Tablet/Capsule Specifications

Code information

Lot #: C5406201, Exp 03/31/2028

Distribution pattern

USA Nationwide