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All product recalls affecting New York.
Includes nationwide recalls (tagged “Nationwide”) and recalls with New York in the distribution area.
Due to a software issue, the software may incorrectly process the date of birth (DoB) received from the Laboratory Information System (LIS) and when the DoB is set to 01/01/1900 or left empty, REMISOL Advance may incorrectly identify a patient as a newborn, affecting the execution of validation rules based on incorrect reference ranges. The test results are not changed by this software defect and are accurately displayed by REMISOL Advance; however, the evaluation flagging of the results may be affected. This issue may lead to wrong reference range calculations and can result in erroneous flagged results being auto validated and uploaded to LIS.
Nova Bus (US) Inc. (Nova Bus) is recalling certain 2022-2023 LFS transit buses. The engine wiring harness may be the incorrect length, which can result in harness damage and a loss of drive power.
Incorrect labeling in which the front red pouch label did not match the actual size of the medical device. The label on the front of the scope incorrectly states 5.0/2.2 while the back label, shipping box and product inside correctly states 5.6/2.8.
A cybersecurity vulnerability was discovered through internal testing.
Vials of implant bone granules may contain less product then specified on labeling.
A cybersecurity vulnerability was discovered through internal testing.
Disconnection of the adapter from the endotracheal tube can potentially be difficult or not possible.
Apic Yamada has recently discovered that certain products may be out of compliance with FDA electronic product regulations in that they did not bear a required label.
Potential for microbial contamination.
Forest River, Inc. (Forest River) is recalling certain 2025 Coachmen Apex and Remote travel trailers. The solar panel wiring may be incorrectly wired to the battery, causing it to melt.
Potential for microbial contamination.
Preset treatment parameters are not consistently being used in accordance with the IFU.
Incorrect product packaged in INSPIRA AIR Balloon Dilation System carton.
This recall involves accessory heaters that are compatible with model years 2023-2025 Honda Pioneer 700 (SXS700), 2022-2024 Pioneer 1000 (SXS1000), and 2022-2024 Talon 1000 (SXS1000S) vehicles. The accessory heaters were sold separately from the vehicles. Affected vehicles have been fitted with the Honda accessory heater system, which has a mounted control panel on the vehicle's dash with controls for air speed, air flow direction and temperature. Customers can enter the vehicle's VIN at https://powersports.honda.com/recalls to see if the vehicle is compatible with the recalled accessory heater. Refer to the Technical Information - Vehicle Identification section in the owner's manual to locate the vehicle's VIN.
This recall involves Ashland 10-inch and 14-inch two-bar right-hand and left-hand casement window hinge tracks installed in windows to allow the windows to be cranked opened and closed. The casement window hinge tracks include part numbers 2003558, 2003559, 2004271 and 2004272. These products can be identified by locating "R10," "L10," "R14" or "L14" located on the face of the casement window hinge track. These hinge tracks were manufactured and sold to residential and commercial window manufacturers in boxes dated April 2024 through December 2024.
This recall involves foldable travel hair dryers. The dryers were sold in blue, pink and purple, and have a red switch with three adjustable gears and an air-collecting nozzle. "Guangmei 3858 hair dryer" is printed on the side of the hair dryer.
This recall involves XZT Huizhou's compact mini hair dryers. The foldable dryers were sold in blue, green, pink and white, and have a white switch with two gear settings and a thermostatic function. "Fashion Hair Dryer" and an image of two animal faces appear on the side of the hair dryer next to a white button with "OK" embossed on it.
Autocar, LLC (Autocar) is recalling certain 2020-2026 DC (Legend) vehicles. The incorrect blower motor fuse may have been installed.
The device was delivered with a preassembled Femoral Augment screw that was missing its thread.
The device was delivered with a preassembled Femoral Augment screw that was missing its thread.