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All product recalls affecting Connecticut.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Connecticut in the distribution area.
This recall involves "The Legendary 'VACATION'" by Vacation Black Label Scented Candles. The product comes in a black glass vessel with an off-white colored fragranced wax. The product is approximately 3.75 inches in diameter by 3.5 inches tall and weighs about one pound. A foil gold color label on the candle states "The Legendary 'VACATION'" by Vacation.
Hemoglobin interference may occur at concentrations lower than the claimed 300 mg/dL, and may cause negatively biased digoxin results.
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2024 RAV4 and 2025 Lexus NX vehicles. Some of the bolts that secure the front brake caliper and the wheel hub bearing may be loose, which can result in a damaged caliper brake hose or possible wheel detachment.
Error on the main label and the patient label. The labels indicate a size XXL, this is a standard-size neck segment.. All further information on the labels is correct (Length, CCD and Offset).
This recall involves certain VINs of Polaris Model Year 2024-2025 RZR XP 1000 and XP 4 1000 ROVs. The recalled vehicles were sold in black, blue, gray, red and white colors. They were sold in two and four-seat configurations. "POLARIS" is stamped on the front grille and "POLARIS" and "RZR" are printed on the sides of the vehicle. The model name is also printed on the side of the chassis. The VIN is located on the vehicle's frame in the left rear wheel well.
BMW of North America, LLC (BMW) is recalling certain 2025 X4 xDrive 30i, X4 M40i and X4 M vehicles. The inner-left roof frame near the head air bag may have a crack that can damage the head air bag during deployment.
Incorrect catheter connector within the kit resulting in inability to provide a secure connection to the epidural catheter. The incorrect catheter connector is smaller than the required catheter connector and therefore is unable to be used to administer medication.
Due to an increase in complaint that the percutaneous reference pin would not fit into the patient reference frame or percutaneous pin adapter.
Instructions for use update on HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 pertaining to Power-on self-test error code "EA POST".
Prestone Products LLC (Prestone) is recalling certain 1-gallon bottles of Prestone DOT 3 Brake Fluid, part number AS402 with date code 2PW24226 manufactured on August 13, 2024. The brake fluid bottles may contain power steering fluid.
Instructions for use update on HotDog Temperature Management Controllers Models WC71, WC77, and Temperature Management Controller MP Model 2083516 pertaining to Power-on self-test error code "EA POST".
Failed Dissolution Specifications
Due to software anomalies that may impact on rod planning specifically, certain optional surgical parameters may have had errors that resulted i incorrect calculations displayed on system. Impacted parameters includes the following: Roussouly Classification, Real Lumbar Lordosis and Real Thoracic Kyphosis, Barrey Ratio, and Lenke Classification.
PACCAR Incorporated (PACCAR) is recalling certain 2024 Peterbilt 367, 389, 548, Kenworth T480, T800, 2024-2025 Peterbilt 520, 567 and Kenworth T880 vehicles with PACCAR 20k steer axles. The steering arm and/or tie rod bracket fasteners may fail, resulting in a loss of steering control.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Nova Bus (US) Inc. (Nova Bus) is recalling certain 2022-2024 LFS buses. The wheelchair securement system may have been installed with the attachment points in the incorrect locations.
Reports of various packaging issues that may result in a breach of the sterile barrier.
Reports of various packaging issues that may result in a breach of the sterile barrier.
International Motors, LLC (International) is recalling certain 2025 EMV vehicles. A circuit breaker may be missing, causing the defrosting system to be inoperative. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 103, "Windshield Defrosting and Defogging Systems."
Platelet Reactivity Test distributed without appropriate US-FDA market clearance; if used healthcare personnel could use the baseline PRUTest measurement prior to initiating drug therapy, and then use the percent inhibition formula in the notice to manually calculate the percentage of platelet aggregation inhibition for a given patient receiving drug treatment with P2Y12 receptor inhibitor.