Exact FDA event identifier

Event 89060

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

Event summary

Timeline bucket: November 19, 2021
Product types: Drug
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Ascent 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

Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325 mg, 100-count bottle, Rx only, Manufactured for: Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, Manufactured by: Ascent Pharmaceuticals, Inc., Central Islip, NY 11722, NDC 31722-997-01.

D-0276-2022

Recall number: D-0276-2022
Initiated: November 19, 2021
Classification: Class II
Status: Terminated
Recalling firm: Ascent Pharmaceuticals, Inc.
Quantity: 9744 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Product Mix-up

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Product Mix-up

Code information

Lot #: 21070817, Exp 6/2023

Distribution pattern

USA Nationwide