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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 82375

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

Open FDA event record

Event summary

Timeline bucket
March 12, 2019
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Akorn 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

Hydrocortisone and Acetic Acid Otic Solution, USP, 10 mL per dropper bottle, Rx only, Hi-Tech Pharmacal Co, Inc., Amityville, NY 11701. NDC: 50383-901-10

D-1011-2019
Recall number
D-1011-2019
Initiated
March 12, 2019
Classification
Class II
Status
Terminated
Recalling firm
Akorn Inc
Quantity
15,322 10 ml bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Sub Potent Drug: OOS results observed for the Hydrocortisone assay during routine stability testing at 12 month controlled room temperature.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Sub Potent Drug: OOS results observed for the Hydrocortisone assay during routine stability testing at 12 month controlled room temperature.

Code information

Lot: 357647, EXP 04/2019

Distribution pattern

Nationwide USA and Puerto Rico