Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
HTO Nevada Inc DBA Kirkman

HTO Nevada Inc DBA Kirkman Recalls

All product recalls associated with HTO Nevada Inc DBA Kirkman.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

583

Class I (Serious)

Most Recent

Dec 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1121–1140 of 10937 recalls

5-MTHF Methylfolate Capsules (Kirkman) – Labeling Error (2024)

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).

Class IIILow

FDAMar 12, 2024CA, FL, IN +4 more• HTO Nevada Inc DBA Kirkman

Eco Terra Hybrid Mattress (Sleep Technologies) – Fire Hazard (2024)

Fire/Burn Risk

This recall involves model ECO TERRA Eco Terra Mattresses manufactured from Aug 5, 2022 to Aug 18, 2022. The mattresses are 10 inches thick with a top panel that is ivory and quilted. The side panel is brown knit quilted with horizontal lines, and the top and bottom tape edges are ivory. The manufacture dates and model name "ECO TERRA" are located on the mattress label, sewn into the cover.

CPSCMar 7, 2024Nationwide• Sleep Technologies Inc., d/b/a The Natural Latex Co. of Camarillo, California

1...55 565758 59...547

Page 57 of 547Next

Clinical Chemistry Calibration Serum (Randox) – Phosphate Bias (2024)

Randox Laboratories has identified that Inorganic Phosphate in Calibration Serum Level 3, CAL2351 & CAL10388, is running with a negative bias on RX Series instruments compared to other methods.

FDAMar 5, 2024Nationwide• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

Neria Soft Infusion Set (Unomedical) – Incorrect Instructions (2024)

Specific lots of Neria Soft Infusion Sets, which have been shipped into the US Market, have been shipped with the incorrect Instruction for Use (IFU) within the final pack. The IFU included is the IFU registered for the Rest of World (ROW) countries. The difference between the US IFU and the ROW IFU is the addition of an intended use section in the ROW IFU.

FDAMar 5, 2024Nationwide• Unomedical A/S Osted Aholmvej 1

Liquid Protein Calibrators (Randox) – Calibration Realignment (2024)

The firm has realigned C3 and Haptoglobin in Liquid Protein Calibrators, IT2691, to reference material ERM-DA470k/IFCC.

FDAMar 1, 2024CA, FL, IL +4 more• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

RayStation Software (RaySearch) – Material Override Error (2024)

A use error that has occurred with RayStation/RayPlan, where material override using Silicon, Si, was incorrectly selected for a silicone gel polymer implant.

FDAFeb 23, 2024Nationwide• RAYSEARCH LABORATORIES AB Eugeniavagen 18c Stockholm Sweden

MATRYX Snowmobiles (Polaris) – Injury Risk (2024)

This recall involves certain Polaris Model Year 2022-2024 MATRYX Voyageur, Indy, Switchback, RMK, and SKS snowmobiles. The recalled snowmobiles were sold in black and custom color combinations and equipped with PATRIOT 650 and 850 engines. The recall also includes primary (drive) clutches sold as service parts with part numbers 1323613 (e-start) and 1323614 (manual start). "POLARIS" is stamped on the front side panel of the vehicles. The VIN and model number are located on the right side of the vehicle's frame. The following models are being recalled: Recalled Model Description Recalled Snowmobiles Model Description Model Year 2022 650 MATRYX VOYAGEUR 146 Model Year 2022 650 MATRYX INDY Model Year 2022 850 MATRYX INDY Model Year 2022 650 MATRYX SWITCHBACK Model Year 2022 850 MATRYX SWITCHBACK Model Year 2022 650 MATRYX RMK Model Year 2022 850 MATRYX RMK Model Year 2023 650 MATRYX INDY Model Year 2023 850 MATRYX INDY Model Year 2023 650 MATRYX SWITCHBACK Model Year 2023 850 MATRYX SWITCHBACK Model Year 2023 650 MATRYX VOYAGEUR 146 Model Year 2023 650 MATRYX SKS 146 Model Year 2023 650 MATRYX RMK Model Year 2023 850 MATRYX RMK Model Year 2024 850 MATRYX RMK

CPSCFeb 22, 2024Nationwide• Polaris Industries Inc., of Medina, Minnesota

Organic Carrot Juice (Barsotti) – Under Processed (2024)

Product was determined to be under processed.

Class IIModerate

FDAFeb 22, 2024AZ, CA, CT +7 more• Barsotti Juice Company, Inc.

HydroFlock Collection Device (Puritan) – Mislabeled Product (2024)

It was discovered through a customer complaint that mislabeled product was distributed. Puritan distributed product labelled as 25-3317-H lot S1014 which contained product code 25-3317-U in all packages.

FDAFeb 21, 2024Nationwide• Puritan Medical Products Company, Llc

Cardiovascular Procedure Kits (Terumo) – Pressure Valve Issue (2024)

Pressure relief valve included in certain lots of cardiovascular procedure kits was reportedly opening at approximately 200-300mmHg versus 400mmHg, potential myocardial tissue damage potentially requiring surgical or medical/pharmacological intervention

FDAFeb 20, 2024Nationwide• Terumo Cardiovascular Systems Corporation