--- title: "HTO Nevada Inc. dba Kirkman Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search HTO Nevada Inc. dba Kirkman recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/hto-nevada-inc-dba-kirkman/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # HTO Nevada Inc. dba Kirkman recall records **3** reported ongoing 4 records in this archive. Latest source date Feb 18, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Feb 18, 2026 FDA drug enforcement ### [FIVE-STAR, VASOCAINE Spray, (Lidocaine HCl 4%, Racepinephrine HCl 0.01%), 4oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-016.](https://isitonrecall.com/recall/fda-drug-d-0385-2026-five-star-vasocaine-spray-lidocaine-hcl-4-racepinephrine-hcl-0-01-4oz-bottles-distributed-by-dermal/) Stability Data Does Not Support Expiry Date. Class II Reported ongoing Distribution: Nationwide within the U.S [Official source for FIVE-STAR, VASOCAINE Spray, (Lidocaine HCl 4%, Racepinephrine HCl 0.01%), 4oz bottles, Distribute...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0385-2026%22) Feb 18, 2026 FDA drug enforcement ### [MAXIMUM, ZONE 1, 4% Lidocaine Cream, 1/2 oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-014.](https://isitonrecall.com/recall/fda-drug-d-0386-2026-maximum-zone-1-4-lidocaine-cream-1-2-oz-bottles-distributed-by-dermal-source-portland-or-97232-ndc-8/) Stability Data Does Not Support Expiry Date. Class II Reported ongoing Distribution: Nationwide within the U.S [Official source for MAXIMUM, ZONE 1, 4% Lidocaine Cream, 1/2 oz bottles, Distributed By: Dermal Source, Portland, OR ...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0386-2026%22) Feb 18, 2026 FDA drug enforcement ### [MAXIMUM, ZONE 2, 4% Lidocaine Cream, (Lidocaine 4% and Epinephrine 0.01%), 1 oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-015.](https://isitonrecall.com/recall/fda-drug-d-0387-2026-maximum-zone-2-4-lidocaine-cream-lidocaine-4-and-epinephrine-0-01-1-oz-bottles-distributed-by-dermal/) Stability Data Does Not Support Expiry Date. Class II Reported ongoing Distribution: Nationwide within the U.S [Official source for MAXIMUM, ZONE 2, 4% Lidocaine Cream, (Lidocaine 4% and Epinephrine 0.01%), 1 oz bottles, Distribu...](https://api.fda.gov/drug/enforcement.json?search=recall_number%3A%22D-0387-2026%22) Mar 12, 2024 FDA food enforcement ### [Kirkman brand 5-MTHF Methyltetrahydrofolate 1mg capsule dietary supplement, Folate 1667mcg DFE, 5000mcg Folic Acid, 120 capsules per package, UPC 8 12325 02354 7. Manufactured e...](https://isitonrecall.com/recall/fda-food-f-1222-2024-kirkman-brand-5-mthf-methyltetrahydrofolate-1mg-capsule-dietary-supplement-folate-1667mcg-dfe-5000mc/) Labeling error. The 5-MTHF 1mg label incorrectly declares 5000mcg Folic Acid instead 1000mcg Folic Acid per serving in the Supplement Facts, but correctly declares Folate 1667mcg DFE. The front label correctly declares product as 5-MTHF Methyltetrahydrofola... Class III Reported terminated Distribution: Distributed in CA, FL, OH, TX, WA and WI and in the following countries China, Netherlands, Pakistan, Peru, Switzerland, and United Kingdom. [Official source for Kirkman brand 5-MTHF Methyltetrahydrofolate 1mg capsule dietary supplement, Folate 1667mcg DFE, 5...](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22F-1222-2024%22) ## Reasons in these listed records - Stability Data Does Not Support Expiry Date. - Labeling error. The 5-MTHF 1mg label incorrectly declares 5000mcg Folic Acid instead 1000mcg Folic Acid per serving in the Supplement Facts, but correctly declares Folate 1667mcg DFE. The front label correctly declares product as 5-MTHF Methyltetrahydrofolate 1mg (or 1000mcg). These examples come from this result page and are not a ranking of every recall reason. ## Checking HTO Nevada Inc. dba Kirkman ### Is there a recall on hto nevada inc. dba kirkman right now? This archive contains 4 records, including 3 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search HTO Nevada Inc. dba Kirkman](https://isitonrecall.com/check/?q=HTO%20Nevada%20Inc.%20dba%20Kirkman) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)