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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 86712

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

Open FDA event record

Event summary

Timeline bucket
October 21, 2020
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
H & H Remedies, 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

Complete imported group

Every recalled product in this event

3 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 3

Union (black) salve packaged in a) 1/8 oz; b) 2 oz.; c) 4 oz.; d) 8 oz.; e) 16 oz.; and f) 32 oz. jars. Mfg & Sold by: H & H Remedies, LLC c/o David A. Cox, 1219 South Broadway, New Philadelphia, OH 44663

D-0071-2021
Recall number
D-0071-2021
Initiated
October 21, 2020
Classification
Class II
Status
Terminated
Recalling firm
H & H Remedies, LLC
Quantity
939 jars

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 #: H20-01S thru H20-12S

Distribution pattern

Nationwide in the United States

drug · product 2 of 3

White Liniment packaged in a) 1 oz; b) 4 oz.; and c) 6 oz bottles. Mfg & Sold by: H & H Remedies, LLC c/o David A. Cox, 1219 South Broadway, New Philadelphia, OH 44663

D-0072-2021
Recall number
D-0072-2021
Initiated
October 21, 2020
Classification
Class II
Status
Terminated
Recalling firm
H & H Remedies, LLC
Quantity
365 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 #: H20-01W thru H20-84W

Distribution pattern

Nationwide in the United States

drug · product 3 of 3

Vapor Ointment packaged in a) 1/8 oz; b) 2 oz.; c) 4 oz.; and d) 8 oz jars. Mfg & Sold by: H & H Remedies, LLC c/o David A. Cox, 1219 South Broadway, New Philadelphia, OH 44663

D-0073-2021
Recall number
D-0073-2021
Initiated
October 21, 2020
Classification
Class II
Status
Terminated
Recalling firm
H & H Remedies, LLC
Quantity
252 jars

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 #: H20-01V thru H20-10V

Distribution pattern

Nationwide in the United States