Exact FDA event identifier

Event 96639

6 recalled-product records grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: April 15, 2025
Product types: Drug
Classifications: Class II
Statuses: Terminated
Recalling firm wording: Pharmadel, LLC

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

6 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 6

DoloDent Maximum Strength Toothache Drops, Homeopathic Oral Drops, 0.50 oz fl (15 mL), Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-400-15

D-0379-2025

Recall number: D-0379-2025
Initiated: April 15, 2025
Classification: Class II
Status: Terminated
Recalling firm: Pharmadel, LLC
Quantity: 9504 bottles

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

Code information

Lot EDD-01

Distribution pattern

drug · product 2 of 6

DoloEar Earache Drops, Homeopathic, 0.50 oz fl (15 mL), Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-401-15

D-0380-2025

Recall number: D-0380-2025
Initiated: April 15, 2025
Classification: Class II
Status: Terminated
Recalling firm: Pharmadel, LLC
Quantity: 27,648 bottles

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

Code information

Lot, expiry: DEE-01, EXP: OCT 26; DEE-02 EXP: FEB 27

Distribution pattern

drug · product 3 of 6

Kingskin, Elimina Las Verrugas, For the removal of common warts, 0.50 oz fl (15 mL), Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-409-15

D-0381-2025

Recall number: D-0381-2025
Initiated: April 15, 2025
Classification: Class II
Status: Terminated
Recalling firm: Pharmadel, LLC
Quantity: 20,048 bottles

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

Code information

Lot, expiry: KSE-01, EXP: OCT 26; KSE-02, EXP: FEB 27

Distribution pattern

drug · product 4 of 6

Rapidol Arnica Gel, Topical Gel, Homeopathic Medicine, 2 oz (57 g), Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-403-02

D-0382-2025

Recall number: D-0382-2025
Initiated: April 15, 2025
Classification: Class II
Status: Terminated
Recalling firm: Pharmadel, LLC
Quantity: 6,048 bottles

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

Code information

Lot, expiry: EAG-01, EXP: MAR 27

Distribution pattern

drug · product 5 of 6

Rapidol Arnica Tablets, Homeopathic Medicine, 100-count bottle, Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-405-99

D-0383-2025

Recall number: D-0383-2025
Initiated: April 15, 2025
Classification: Class II
Status: Terminated
Recalling firm: Pharmadel, LLC
Quantity: 6,048 bottles

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

Code information

Lot, expiry: EAT-01, EXP: MAR 27

Distribution pattern

drug · product 6 of 6

Urodel, Urinary Tract Infection Symptoms Relief, Homeopathic, 30 chewable tablets per bottle, Distributed by: Pharmadel, New Castle, DE 19720, NDC 55758-406-30

D-0384-2025

Recall number: D-0384-2025
Initiated: April 15, 2025
Classification: Class II
Status: Terminated
Recalling firm: Pharmadel, LLC
Quantity: 10,752 bottles

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

Code information

Lot, expiry: UDE-01, EXP: OCT 26