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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 79172

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

Open FDA event record

Event summary

Timeline bucket
February 07, 2018
Product types
Drug
Classifications
Class III
Statuses
Terminated
Recalling firm wording
Webrx dba RxPalace.com

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

BonaDur For Men (lidocaine) spray, 10 mg per spray, Net Contents .25 fl. oz. (7.4 mL) spray bottles, Manufactured by WebRx Pharmacy Palace, Sarasota, FL 34232; NDC 70582-999-74

D-0421-2018
Recall number
D-0421-2018
Initiated
February 07, 2018
Classification
Class III
Status
Terminated
Recalling firm
Webrx dba RxPalace.com
Quantity
1 bottle

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
CGMP Deviations

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

CGMP Deviations: not manufactured according to current good manufacturing practices.

Code information

Lot: 17JXIII, Exp. 12/31/2019

Distribution pattern

NY