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All product recalls affecting Idaho.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Idaho in the distribution area.
This recall involves P.J. Salvage Kids Checker Plush Short Sets, Fleece Pajama Sets, Smiley Plush Robes and Tie Dye Plush Sets. The Girl's Checker Plush Short Set, model RP3KHST, is a pullover hoodie with a kangaroo pocket, long pants and shorts, and was sold in gray with stars and lilac with checkers. The Kid's Fleece Pajama Set, model RP3KPST, is a pullover crew with a kangaroo pocket and jogger pants and was sold in a multi color tie dye pattern. The Girl's Smiley plush robe, model RP3KPR, is a hooded robe with front pockets and a waist tie and was sold in pink lilac with smiley faces. The Girl's Plush sets, model RP3KFST, is a fleece set with a pullover crew top and jogger pants and was sold in lilac ice with a "Smile" graphic on the front, in multi color with a "Good Vibes" graphic on the front and in sky blue with a "Sunshine" graphic on the front. They were sold in children's sizes S-XL. The sizes and "P.J. Salvage" are printed on the neck label. The side seam label has care instructions, fiber content, and country of origin information.
A software defect in Version 7.9 of the pump software for Tandem t:slim X2 and Tandem Mobi pumps, when used with Control IQ+ technology, will cause the pump to incorrectly interpolate glucose trends when the Estimated Glucose Value (EGV) is above 255 mg/dL at the start or end of a gap in data collection due to a lapse in connection from a paired continuous glucose monitor (CGM) sensor, which can lead to under-delivery or over-delivery of insulin based on inaccurate result leading to severe cases of hypoglycemia or hyperglycemia.
The "Use with plate 7, 8, 9, 10" compatibility statement on top of the label does not match with the compatibility statements "USE WITH PLATE 5, 6" in the translations section of the same label.
Beckman Coulter has received complaints of erroneous Vitamin B12 results when using Access Vitamin B12 Reagent lot 439850. The affected reagent lot may cause erroneously low or high Vitamin B12 results, leading to a delayed or improper diagnosis and/or repeat testing.
REV Recreation Group (REV) is recalling certain 2022-2025 Fleetwood Bounder, Flair, Fortis, Holiday Rambler Admiral, Invicta, Vacationer, 2023-2025 Fleetwood Flex, Holiday Rambler Eclipse, and 2022-2023 Fleetwood Southwind motorhomes. The engine exhaust tip may detach, allowing exhaust fumes to enter the cabin.
A software defect in Version 7.9 of the pump software for Tandem t:slim X2 and Tandem Mobi pumps, when used with Control IQ+ technology, will cause the pump to incorrectly interpolate glucose trends when the Estimated Glucose Value (EGV) is above 255 mg/dL at the start or end of a gap in data collection due to a lapse in connection from a paired continuous glucose monitor (CGM) sensor, which can lead to under-delivery or over-delivery of insulin based on inaccurate result leading to severe cases of hypoglycemia or hyperglycemia.
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2021-2023 ID.4, 2022-2023 Audi Q4 e-Tron, and Q4 e-Tron Sportback vehicles. The instrument panel may not properly display the transmission gear lever indicator. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 102, "Transmission Shift Lever Sequence, Starter Interlock, and Transmission Braking Effect."
This recall involves all Canyon Speedmax CF triathlon bicycle models R073 and R41 with V21 aerostems. The carbon fiber bikes were sold in black/red, black/blue, gray/orange, and red and black. "Canyon" is printed on the downtube. "Speedmax" is printed on the top tube. "V21" is printed on the left side of the stem. The model number can be found on a sticker at the top of the seat tube, just below the saddle.
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 TRUBLUE iQ Auto Belay Devices, which enable climbers to safely descend while climbing. The TRUBLUE iQ is gray with blue handles and a gray sash on the front cover. The TRUBLUE iQ+ has an added catch-and-hold brake on the front. The LT versions of the iQ and iQ+ have blue tags above the blue webbing hand grip; the XL versions have a purple tag. The recalled auto belay devices have a serial number within the following serial number ranges printed on the device's handle, as well on the bottom of the device: Products Models Serial Number Range TRUBLUE iQ LT TBiQ LT (12.5m) iQ0041591 through iQ0044486 TRUBLUE iQ+LT TBiQ+ LT (12.5m) iQP000401 through iQP000422 TRUBLUE iQ XL TBiQ XL (20m) iQXL01283 through iQXL03425 TRUBLUE iQ+XL TBiQ+ XL (20m) iQXLP0104 through iQXLP0215
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
Aspiration catheter distal tip features and characteristics may not be in the scope of FDA clearance; tip detachment, vessel rupture, and vasospasm could occur.
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.