HTO Nevada, Inc. Recalls

Overview of recall records associated with HTO Nevada, Inc., including dates, categories and classifications where available.

2recall records

Feb 22, 2023latest record date

Feb 22, 2023earliest record date

Recall history in this database

Classification mix: Class II: 2.

DrugFeb 22, 2023

HTO Nevada Maximum Zone2 Topical Analgesic, 1oz bottle, for use during a pain sensitive recall — FDA D-0271-2023

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

Class IIFDA: TerminatedHTO Nevada, Inc.

DrugFeb 22, 2023

HTO Nevada New & Improved Blue Gel Anesthetic, to reduce pain and swelling during pain recall — FDA D-0270-2023

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

Class IIFDA: TerminatedHTO Nevada, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies HTO Nevada, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.