Loading...
Loading...
All product recalls associated with KZRV.
Total Recalls
398
Past Year
21
Class I (Serious)
8
Most Recent
Nov 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.
KZRV, L.P. (KZRV) is recalling certain 2018-2022 Camplite, Confluence, Connect, Connect SE, Connect Lite, Durango, Durango Gold, Durango Half Ton, Durango Sport, Durango 1500, Quicksilver, Sonic, Sonic X, Sportsmen, Sportsmen FW, Sportsmen LE, Sportsmen SE, Sportsmen Sportster, Sportster, SportTrek, SportTrek Touring, Spree, Stratus, Venom, and Venom V Series recreational vehicles, equipped with Winntec model 6020 two-stage propane regulators. The regulator may fail, causing an increase in propane pressure.
Potential for difficulty in safety mechanism activation.
Potential for difficulty in safety mechanism activation.
This recall involves six styles of Tkala Fashion 100% cotton children's pajamas. They were sold in sizes 1-8 Years, 10 Years and 12 Years, and in the following prints: Multi-color dinosaur, orange and white dinosaur, gray shark, green dinosaur, black and white dinosaur, and black rocket ship. The two-piece pajamas have short sleeves. "100% cotton" and the care instructions are printed on the inside of the top.
KZRV, L.P. (KZRV) is recalling certain 2021 Connect travel trailers. The trailer tongue weight is too low, which may not apply enough downward force to the hitch of the tow vehicle, causing the trailer to be unstable at highway speeds.
The IndiGo power cord might wear during use which could lead to its damage, resulting in the cord being cut, burnt or short circuit with limited emission of sparks.
KZRV, L.P. (KZRV) is recalling certain 2018-2019 KZ RV Sidewinder vehicles equipped with a Winntec model 6020 two-stage propane regulator. The regulator may fail, causing an increase in propane pressure.
The devices have a different inner diameter than the diameter specified on the outer box label.
KZRV, L.P. (KZRV) is recalling certain 2021 Stratus and SportTrek trailers. The water heater circuits were wired with an incorrect size circuit breaker, which may prevent the breaker from tripping, and failing to provide adequate wiring protection.
Inability for the user to inject the paste from the syringe into the target location.
KZRV, L.P. (KZRV) is recalling certain 2021 Sportsmen Classic, Escape, and Sonic recreational trailers. The microwave circuits were improperly connected to a 20amp circuit breaker instead of a 15amp circuit breaker.
This recall involves Gorilla Commerce heavy duty oven liners. The black fiberglass liners were sold in a set of three. Extra Thick and Gorilla Grip with a gorilla logo is printed on the packaging.
The device has the potential to release nickel above the acceptable margin of safety in pediatric patients who weigh less than 20 kg (44.09 lbs) when 2 or more implants are used.
Product may be mislabeled.
Product may be mislabeled.
This recall involves 4-drawer chests with plastic drawer glides sold by Transform under the Essential Home brand and identified as the "Belmont 2.0" model. The chests measure approximately 29.8 inches in height and 27.7 inches in width, and were sold in four colors including black, pine, walnut, and white. The manufacturer's name, "Kappesberg Moveis," and the model number "F214" can be found on the instruction manual that came with each chest. Kmart Item Number Mfr. Model Number UPC Color 01832577-9 F214-PRF 7-89515563264-9 Black 01832593-6 F214-MEF 7-89515563273-1 Pine 01832637-1 F214-WAF 7-89515563285-4 Walnut 01833166-0 F214-BRF 7-89515590807-2 White
Updated sterilization instructions are being provided to ensure 1) a specific sterilization tray is not used, and 2) ethylene oxide sterilization is never used on certain reusable flexible intubation endoscopes with total lumen lengths greater than 850mm. Incompletely sterilized endoscopes might introduce infectious agents into patient airways, resulting in infection.
Updated sterilization instructions are being provided to ensure 1) a specific sterilization tray is not used, and 2) ethylene oxide sterilization is never used on certain reusable flexible intubation endoscopes with total lumen lengths greater than 850mm. Incompletely sterilized endoscopes might introduce infectious agents into patient airways, resulting in infection.
Updated sterilization instructions are being provided to ensure 1) a specific sterilization tray is not used, and 2) ethylene oxide sterilization is never used on certain reusable flexible intubation endoscopes with total lumen lengths greater than 850mm. Incompletely sterilized endoscopes might introduce infectious agents into patient airways, resulting in infection.
Modular Junction Box (MJB) cables can melt and affect the bed functionality.