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All product recalls affecting New York.
Includes nationwide recalls (tagged “Nationwide”) and recalls with New York in the distribution area.
The recalled bed rails have model numbers MDS6800BA and MDS6800BAH. The two models are identical, but model MDS6800BA was sold individually and model MDS6800BAH was sold in cases of three units. The bed rails are made of black metal tubing with a rounded black foam rubber grip handle and a fabric pouch. The name "Medline" and the model number are printed on a label located on the support frame of the bed rail near the vertical portion of the bed rail.
This recall involves the ADIOS! Super Vinegar All Natural Cleaner, 30%. The cleaner's bottles are labeled on the front with: "ADIOS! SUPER VINEGAR ALL NATURAL CLEANER. 30% Concentrate Indoor & Outdoor use". There is a label on the back with: "Say ADIOS to industrial cleaners with the natural power of vinegar" along with safety information and instructions. The product was sold in a 16 oz. white bottle with a blue cap.
This recall involves padded crib bumpers sold in the following colors: gray with white clouds, teddy bear, light pink, and white. They were sold in a clear plastic bag. There are no markings or labeling on the crib bumpers.
CGMP Deviations
Failed Dissolution Specifications
Failed Dissolution Specifications
CGMP Deviations
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2022-2023 Tundra and Lexus LX600 vehicles equipped with a V35A engine. Debris from the manufacturing process may contaminate the engine and cause the main bearings to fail, which can result in an engine stall and loss of drive power.
Smiths Medical has identified that the securement flange of specific lots of the Bivona Neonatal/Pediatric and Adult Tracheostomy products may tear because of a manufacturing defect.
Potential for certain Life2000 ventilator systems to either fail to charge or have intermittent charging behavior due to damage to the battery charger dongle. Damage of the battery charger dongle prevents the ventilator's internal battery from charging.
Potential for the CUSA Excel 23KHz Straight Handpiece housing to crack, may result in delay of treatment
Lion Electric Company (Lion Electric) is recalling certain 2024-2025 LionC school buses. The parking brake may malfunction and allow the lever to be released without pressing the release button.
The recall is prompted by a defective charger unit (0970.2873) for models 1133.22B4, 1133.22B5, and 1133.22F5 of the ALPHAMAXX mobile operating table. This issue poses a risk of inadequate charging and operational failure.
American Furukawa submitted a defect information report based upon the recall determinations made by Toyota (23V-480), Ford (23V-847), and Chrysler (FCA US, LLC) (Stellantis) (24V-199, 24E-025). Certain clock springs installed in steering column control modules may have been contaminated during the manufacturing process, which can cause electrical failure and deactivate the driver's air bag.
Navistar, Inc. (Navistar) is recalling certain 2024-2025 IC Bus CE school buses. The brake lights, in certain conditions, may not illuminate when the brake pedal is depressed, due to a software error. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 121, "Air Brake Systems."
Karma Automotive (Karma) is recalling certain 2020-2022 Revero GS-6, Revero GS-6s, Revero GS-6L, Revero GTS, and Revero GT vehicles. A communication error with the vehicle control module (VCM) may cause the front turn signals to fail intermittently. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 108, "Lamps, Reflective Devices, and Associate Equipment."
Grand Design RV, LLC (Grand Design) is recalling certain 2023 Solitude fifth wheels. Loose or missing fasteners on the refrigerator cooling unit can allow excessive movement of the unit, possibly causing the propane line to crack and leak.
Cardinal Health is following the FDA's recommendations regarding the disposition of affected Jiangsu Shenli Medical Production Co. Ltd (Shenli) Syringes in the Merit Medical supplied finished kits. Merit Medical supplied finished kits are included as components in Presource kits. According to the FDA s communication, these Shenli syringes, located inside a Merit Medical kit component, cannot be distributed for use as they could contain a significant change or modification in design which could significantly alter the safety or effectiveness of the finished kit product, resulting in the risk of patient harm such as inaccurate dosing and a leaking device.
Smiths Medical has identified that the securement flange of specific lots of the Bivona Neonatal/Pediatric and Adult Tracheostomy products may tear because of a manufacturing defect.
Grafts were found to have been approved, released, shipped and implanted with an invalid test results.