Exact FDA event identifier

Event 78051

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

Event summary

Timeline bucket: August 29, 2017
Product types: Drug
Classifications: Class I
Statuses: Terminated
Recalling firm wording: Lucky Mart 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

PIYANPING Anti-Itch (hydrocortisone) Lotion, 1%, Net Wt. 0.67 oz (20g) tube, Manufactured By: Jimin Pharmaceutial Co., LTD., Distributor: Lucky Mart, El Monte, CA 91733, NDC 68085-8012-4.

D-0031-2018

Recall number: D-0031-2018
Initiated: August 29, 2017
Classification: Class I
Status: Terminated
Recalling firm: Lucky Mart Inc.
Quantity: 13,800 tubes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Incorrect Product Formulation: product contains dexamethasone instead of hydrocortisone.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Incorrect Product Formulation: product contains dexamethasone instead of hydrocortisone.

Code information

Lot #: C16001, C16002, Exp 12/18

Distribution pattern

Nationwide in the USA