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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 91694

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

Open FDA event record

Event summary

Timeline bucket
February 09, 2023
Product types
Drug
Classifications
Class II
Statuses
Terminated
Recalling firm wording
HTO Nevada, 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

2 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 2

New & Improved Blue Gel Anesthetic, to reduce pain and swelling during pain sensitive procedures, 1 oz bottle, distributed by Dermal Source, Portland, OR, www.dermalsource.com 1-888-568-3223. NDC Code: 80069-008-01. Drug Facts- For use by licensed professionals only, Active Ingredients -Lidocaine HCL (5%), Tetracaine HCL (1%) and epinephrine (0.1%).

D-0270-2023
Recall number
D-0270-2023
Initiated
February 09, 2023
Classification
Class II
Status
Terminated
Recalling firm
HTO Nevada, Inc.
Quantity
4709 bottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
cGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

cGMP Deviation: Raw material recalled by repackager, due to discoloration of the epinephrine API.

Code information

Lot #s: 796CP-0006, Exp 02/2024; 796CP-0007, Exp 03/2024.

Distribution pattern

Nationwide in the USA and Canada.

drug · product 2 of 2

Maximum Zone2 Topical Analgesic, 1oz bottle, for use during a pain sensitive procedure, distributed by: DERMAL SOURCE, Portland, OR, www.dermalsource.com, 1-866-568-3223, NDC code: 80069-012-01, Drug Facts- For use by licensed professionals only' Active Ingredients- Lidocaine HCL (5%), Epinephrine (0.01%).

D-0271-2023
Recall number
D-0271-2023
Initiated
February 09, 2023
Classification
Class II
Status
Terminated
Recalling firm
HTO Nevada, Inc.
Quantity
1,571 bottles

App-derived interpretation

Manufacturing or process control reason.manufacturing_process_control · v1.0.0
cGMP Deviation

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

cGMP Deviation: Raw material recalled by repackager, due to discoloration of the epinephrine API.

Code information

Lot #: 795CP-0003, Exp 07/2024.

Distribution pattern

Nationwide in the USA and Canada.