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All product recalls affecting Kansas.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Kansas in the distribution area.
This recall involves ARVA Neo BT Pro Avalanche Transceivers. The transceivers are black plastic with an LCD screen below a red mark button. NEO BT PRO is written on the left side of the device. The affected beacons have serial numbers NBP00052-1027 to NBP00287-1127 and NB00300-1127 to NB11675-0329. The serial number is located inside the battery compartment on the underside of the battery compartment lid.
This recall involves model number 98715 Goal Zero 4x HPP to 1x HPP+ Solar Series Combiner, a cable for chaining multiple solar panels in series into one output for charging a battery. The combiner cable is a black plastic cable with four high power port (HPP) connectors on one end and one HPP on the other end. The portable panels fold out and are set up by consumers. They are designed for camping and other applications.
This recall involves Ellerbeck Wall Sconces. The wall sconces have articulating jointed arms and can be mounted either as a plug-in fixture, without an electrical box, or without a cord to an electrical box. The sconce arms measure about 21.25 inches long. The wall sconces were sold in black, natural brass, polished nickel and classic pewter finishes with model numbers 43115BK, 43115NBR, 43115PN and 43115CLP. The model number and production date are printed on the product packaging and on a sticker on the inside of the wall plate. Only wall sconces produced on or after June 16, 2023, installed as a plug-in fixture without an electrical box are included in this recall. The production date code is located on a sticker on the underside of the sconce wall plate.
This recall involves Style Life Eleven baby loungers. The loungers include a head pillow and fold into a portable handbag with a handle. When folded into the portable handbag, the brand name "Style Life Eleven" is visible on a white square in cursive font. The loungers were sold in different printed fabrics including Dinosaur, Blue & White Crowns, Dotted Pink, Dotted White & Purple, Zoo Animals, and Gray & Brown Crowns. Only portable loungers purchased on or after June 23, 2022, are included in this recall.
This recall involves 20 different styles of Forever 21 children's pajamas: eight pant styles, three short styles and nine two-piece pajama set styles. The pajamas were sold in children's sizes 5/6, 7/8, 9/10, 11/12 and 13/14. The size and "Forever 21" are printed on the red, black or pink label at the neck or waist of the pants and shorts. The pajamas have the following item number located on a sewn-in, side-seam label below the bar code: Pajama Product Item number White pants with pink bows 01298115 Black and white Minnie Mouse polka dot boxer shorts 01287805 Minnie Mouse white cami and print pants 01287794 Hello Kitty pink and blue stripes shirt and shorts 01299151 Black, gray and white plaid pants 01298112 Blue plaid shorts 01285181 Lavender and pink plaid shirt and shorts 01323034 Cream with teddy bear print pants 01298113 Beetlejuice print pants 01322007 Gray Beetlejuice print shirt and pants 01323269 Mickey Mouse print pants 01297198 Dalmatian print pants 01322009 Red plaid pants "Be Mine" pink and red hearts tee and shorts 01249379 "Just keep Growing" white cami and floral shorts 01261320 "Too Cute" white t-shirt and floral Shorts 01263030 Pink Hello Kitty print cami and shorts set 01274432 Sanrio Keroppi print tee and shorts 01274433 White and blue floral shorts 01285168
The hardness not meeting the material specification and may cause the diamond bur to bend.
Stability data does not support expiry: the products have the potential to be out of specification at the time of expiry of 36-months.
Stability data does not support expiry: the products have the potential to be out of specification at the time of expiry of 36-months.
Orange EV is recalling certain 2023-2024 HUSK-e XP terminal trucks. The rear Gross Axle Weight Rating (GAWR) on the federal placard is incorrect and the installed tires and rims may be inadequate for the truck's intended use. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 120, "Wheels and Rims - Other Than Passenger Cars."
Due to an increase in complaints concerning foot tray pedal spring failing resulting in the pedal remaining pressed
Beckman Coulter has determined that device software versions V1.3, V1.4, V1.4.1, V1.4.2, V1.4.3. have a defect due of which, when all constituent tests of a calculated result are rerun, either manually ordered by the operator at the analyzer or automatically triggered by predefined rules in System Configuration, the calculated result will not be recalculated using the constituent tests rerun results. The system will report only the calculated result using the initial constituent tests results to the operator and LIS/Remisol. The issue was identified by Beckman Coulter internal engineering testing. The defect may cause a delay in reporting patient results.
Tracheostomy tube with cuff reusable inner cannula has a flange that may disconnect from the outer cannula of the device, which could cause respiratory failure, aspiration, unspecified tissue injury, aspiration, respiratory tract infection, bronchospasm, a delay to treatment and/or death.
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
A wireless foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation.
There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.
There is a potential for blister seals on the product to present a bubble on the seal area of the packaging. This seal acts as a sterile barrier and, in this event, indicates that the sterility seal has been breached.
There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.