HTO Nevada recalls

HTO Nevada has 6 recalls on record with the FDA and USDA, the earliest in 2023 and the latest reported on 11 Mar 2026. 3 are still ongoing. 3 were reported in the last 12 months. The most frequent reason is potency & assay.

Total recalls6since 2023

Last 12 months3reported

Class I00% of total

Ongoing3latest 11 Mar 2026

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 3 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 5 83%Class III 1 17%

Why hto nevada is recalled

Product types

Pain Medication583%
Vitamins117%

By year

2026350%
2024117%
2023233%

Ongoing hto nevada recalls

3 active

Reported	Class	Recall	Company	Reason	Where
11 Mar 2026Drug	CLASS II	Maximum, Zone 1, 4% Lidocaine Cream recalled by HTO Nevada	HTO Nevada	Potency & Assay	Nationwide
11 Mar 2026Drug	CLASS II	Maximum, Zone 2, 4% Lidocaine Cream, (Lidocaine recalled by HTO Nevada	HTO Nevada	Potency & Assay	Nationwide
11 Mar 2026Drug	CLASS II	Five-star, Vasocaine Spray, (Lidocaine HCl recalled by HTO Nevada	HTO Nevada	Potency & Assay	Nationwide

All hto nevada recalls, newest first

6 total

Reported	Class	Recall	Company	Reason	Where
11 Mar 2026Drug	CLASS II	Maximum, Zone 1, 4% Lidocaine Cream recalled by HTO Nevada	HTO Nevada	Potency & Assay	Nationwide
11 Mar 2026Drug	CLASS II	Maximum, Zone 2, 4% Lidocaine Cream, (Lidocaine recalled by HTO Nevada	HTO Nevada	Potency & Assay	Nationwide
11 Mar 2026Drug	CLASS II	Five-star, Vasocaine Spray, (Lidocaine HCl recalled by HTO Nevada	HTO Nevada	Potency & Assay	Nationwide
15 May 2024Food	CLASS III	Kirkman brand 5-MTHF Methyltetrahydrofolate 1mg capsule recalledKirkman	HTO Nevada	Labeling Errors	6 states
22 Feb 2023Drug	CLASS II	New & Improved Blue Gel Anesthetic, to reduce pain recalled	HTO Nevada	Manufacturing (CGMP) Deviations	Nationwide
22 Feb 2023Drug	CLASS II	Maximum Zone2 Topical Analgesic recalled by HTO Nevada	HTO Nevada	Manufacturing (CGMP) Deviations	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.