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All product recalls affecting South Dakota.
Includes nationwide recalls (tagged “Nationwide”) and recalls with South Dakota in the distribution area.
This recall involves wicker-style armchairs with plastic cross weave on the seat, back and sides, and dark metal frames. The recalled armchairs were sold in green/white color combination (SKU number 400266563392) or in gray/white color combination (SKU number 400266563330), and measure about 33 inches tall, 28 inches deep, and 26 inches wide. The SKU number can be found on a sticker attached to the chair's leg, and on a hangtag attached to the back of the chair.
This recall involves Best Lighting Products LEDFHB line of high bay light fixtures in 90, 105, 135, 178, 180, 215, 265, 320 and 425 watts. These lights were sold in white, and are typically used in commercial settings, such as warehouses and facilities with high ceilings. The following model numbers are included in this recall: LEDFHB90, LEDFHB105, LEDFHB135, LEDFHB178, LEDFHB180, LEDFHB215, LEDFHB265, LEDFHB320 and LEDFHB425. The model name and number can be found on a label on the back of the recalled fixtures.
This recall involves Lovely Angel children's lace nightgowns sold in six colors, including black, lavender, watermelon, beige, green and red. The short-sleeved nightgowns have white lace trim on the chest area and on the bottom hem, and a white ribbon bow at the collar. They were sold in children's sizes ranging from 3Y to 12Y. A side seam label states the following: "100% Rayon", washing instructions, manufacturer name "Tong Tai clothing co., Ltd", "Made in china", "Huang mei, HuBei", lot number 021123, and manufacture date "11/2023".
Hyundai Motor America (Hyundai) is recalling certain 2024 Santa Fe vehicles. A software error in the transmission control unit may result in a vehicle roll away when the vehicle is in PARK.
Due to guidewires being manufactured incorrectly with the guidewires being mis-assembled within the hoop such that the proximal (stiff) end of the guidewire is located at the distal end of the hoop. Injury could occur if the user attempts to insert the proximal end into the patient.
Due to a software issues, after the instrument processes 250 racks cumulatively, any subsequent racks with samples requiring rerun/reflex will be held in the Sample Handler's Buffer area and and error code "9000" will be reported. This issue may cause a delay of results.
Beckman Coulter is recalling the DxI 9000 Access Immunoassay Analyzer due to undersized Pneumatics Tubing in the reagent storage module causing air leaks, compressor failures or sample processing errors. Four complaints were filed for this event that led to Beckman Coulter finding undersized tubing in stock and initiated corrective actions. Use of the affected device may result in errors leading to delay of results.
The reason for this recall is QuidelOrtho has determined that during normal use the VITROS XT ALB-TP Slides may shed dust and debris as they travel through the MicroSlide Subsystem of the VITROS XT 3400 or VITROS XT 7600 analyzer. This dust and debris may then settle onto VITROS Na+ (Sodium) Slides as they are processed through the same MicroSlide Subsystem, potentially resulting in an increase in non-reproducible, positively, or negatively biased Na+ results. The level of bias will depend on where the dust and debris settle on the Na+ MicroSlide and may impact Na+ measurements to varying degrees inside and outside of the measuring range depending on the amount of contamination. All of which could vary from no/low bias with no patient harm, to extreme bias (falsely elevated or reduced results) potentially resulting in incorrect diagnosis; treatment; and/or a serious patient health hazard (for example, hypernatremia or hyponatremia). This issue may also potentially generate error codes preventing the analyzer from processing the MicroSlide Assays and cause delay of the patient results. All current and expired VITROS XT Chemistry Products ALB-TP slides are affected by this issue.
The weld on the light head frame can crack which could lead to problems such as the light head frame sagging, the plastic front face housing cracking, or the light head detaching.
Due to software issue, there is a potential when a restock label is printed for a medication stored in a non-CUBIE location, that the incorrect bin for the medication is printed on the label.
Battery management system within Laryngoscope devices may deplete below the deign threshold which may result in thermal event followed by risk of explosion.
Specific lots of TruDi NAV Suction Instruments 0 Degrees were incorrectly calibrated which when used with the TruDi Navigation System, may result in a discrepancy between the actual tip location and the visualized location displayed on the system.
Specialty Manufacturing Co. (Safe Fleet) submitted a defect information report based upon the recall determinations made by Gillig, LLC (23V-812) and BYD Coach & Bus (24V-374). The fuse in the mirror control switch may be under-rated for the vehicle application, which can result in the switch overheating in the event of a short-circuit or voltage spike.
Keystone RV Company (Keystone) is recalling certain 2024 Springdale 245ML, Hideout 24L0F, Aspen Trail 260THLOFT, 360THLOFT, and Colorado 360THLOFT travel trailers. The metal sidewall may be incorrectly attached and come loose during transit.
During manufacturing, DLP Single Stage Venous Cannulae - straight tip (Model 66118) was incorrectly placed into a product labeled as DLP Single Stage Venous Cannulae - right angle metal tip (Model 67312).
The weld on the light head frame can crack which could lead to problems such as the light head frame sagging, the plastic front face housing cracking, or the light head detaching.
The weld on the light head frame can crack which could lead to problems such as the light head frame sagging, the plastic front face housing cracking, or the light head detaching.
Volvo Bus Corporation (Volvo Bus) is recalling certain 2024 Volvo 9700 vehicles. The castellated nuts securing the steering gear link rod to the steering arm and/or the pitman arm may not have been tightened properly, which can allow it to loosen.
Battery management system within Laryngoscope devices may deplete below the deign threshold which may result in thermal event followed by risk of explosion.
IFU update to address device's battery handling information.