Product Recalls Today
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
Track recent product recall alerts from official U.S. sources. Filter by recall date, source agency, risk level and product category to find newly published food, vehicle, baby product, medical device and consumer product recalls.
Search recent recall notices by product name, brand, UPC, lot code, model number, source agency or official recall number.
| Product Recall | Source | Type | Risk | Date | Action |
|---|---|---|---|---|---|
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Power Rear Seats May Trap a Person
Hyundai Motor America (Hyundai) is recalling certain 2026 Palisade and 2026 Palisade Hybrid vehicles equipped with a Limited or Calligraphy trim package. The second and third row power seats may fail to detect a person. The seat may continue to move after contacting a person during powered seat functions, such as one-touch tilt-and-slide or automatic power fold-and-stow. A person, especially a child, may become trapped by a rear powered seat, increasing the risk of injury or death.
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NHTSA
26V160000
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Vehicle | High |
Mar 17, 2026
Recall: Mar 17, 2026
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Details |
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Reduced Visibility from Black Tint on Windows/FMVSS 205
Ferrari North America, Inc. (Ferrari) is recalling certain 2025-2026 12Cilindri vehicles. The rear and side windows have less than 70% light transmittance which can obscure the driver's visibility. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 205, "Glazing Materials." Windows with insufficient light transmittance can impair the driver’s visibility, increasing the risk of a crash.
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NHTSA
26V152000
|
Vehicle | High |
Mar 16, 2026
Recall: Mar 16, 2026
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Details |
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Training Seat May Fail/FMVSS 207, 210
Orange EV (OEV) is recalling certain 2022-2023 T-Series Pure Electric Terminal Trucks, 2023-2025 e-TRIEVER, and 2023-2026 HUSK-e terminal trucks. The optional foldaway training seat may fail. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard numbers 207, "Seating Systems" and 210, Seat Belt Assembly Anchorages." A seat that fails may not properly restrain an occupant during a crash, increasing risk of injury.
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NHTSA
26V153000
|
Vehicle | High |
Mar 16, 2026
Recall: Mar 16, 2026
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Details |
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Insufficiently Welded Front Seat Frames/FMVSS 207, 210
Nissan North America, Inc. (Nissan) is recalling certain 2026 Kicks and Sentra vehicles. The hook bracket of the front seat frames may be insufficiently welded, which can cause the front seat frames to become loose. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) numbers 207, "Seating Systems" and 210, "Seat Belt Assembly Anchorages." A loose seat may not restrain the occupant as intended, increasing the risk of injury during a crash.
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NHTSA
26V145000
|
Vehicle | High |
Mar 13, 2026
Recall: Mar 13, 2026
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Details |
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SCM Software Error May Cause Unintended Vehicle Movement
Cummins, Inc. (Cummins) is recalling certain PD7000 Electric Drive, part number BES CM0904 EV104B. The System Control Module (SCM) software error may cause a stationary vehicle to move unexpectedly. Unintended vehicle movement increases the risk of a crash.
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NHTSA
26E011000
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Vehicle | High |
Mar 13, 2026
Recall: Mar 13, 2026
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Details |
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Wheelchair Tie-Down May Not Lock
Corp. Micro Bird, Inc. (Micro Bird) is recalling certain 2002-2015 MB II, 2008-2026 G5, and 2015-2026 T-Series transit buses. An installation error may prevent the wheelchair tie-downs from locking, leaving the wheelchair improperly secured. An unsecured wheelchair can move during transit or a crash, increasing the risk of injury.
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NHTSA
26V147000
|
Vehicle | High |
Mar 13, 2026
Recall: Mar 13, 2026
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Details |
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Wheelchair Tie-Down May Not Lock
Micro Bird USA LLC (Micro Bird) is recalling certain 2026 G5 transit buses. An installation error may prevent the wheelchair tie-downs from locking, leaving the wheelchair improperly secured. An unsecured wheelchair can move during transit or a crash, increasing the risk of injury.
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NHTSA
26V148000
|
Vehicle | High |
Mar 13, 2026
Recall: Mar 13, 2026
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Details |
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Wheelchair Tie-Down May Not Lock
Corp. Micro Bird, Inc. (Micro Bird) is recalling certain 2003-2026 MB II, 2006-2026 G5, and 2015-2026 T-Series school buses. An installation error may prevent the wheelchair tie-downs from locking, leaving the wheelchair improperly secured. An unsecured wheelchair can move during transit or a crash, increasing the risk of injury.
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NHTSA
26V149000
|
Vehicle | High |
Mar 13, 2026
Recall: Mar 13, 2026
|
Details |
|
Incorrect Low Tire Pressure on Certification Label
Altec Industries, Inc. (Altec) is recalling certain 2023-2026 Service Body, Aerial Device, Pressure Digger, Spray Truck, and Digger Derrick vehicles. The low tire pressure rating printed on the final stage certification label is incorrect. An incorrect pressure rating may lead to underinflated tires, increasing the risk of a tire blowout or a crash.
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NHTSA
26V150000
|
Vehicle | High |
Mar 13, 2026
Recall: Mar 13, 2026
|
Details |
|
Software Error May Cause Unintended Acceleration or Deceleration
New Flyer of America, Inc. (New Flyer) is recalling certain 2021-2025 XE35, 2021-2026 XE40, 2023-2025 XE60, 2023-2026 XHE40, and 2024-2026 XHE60 transit buses equipped with Accelera ELFA 3 control systems V1 and V2. An inverter software error may cause unintended acceleration or deceleration in certain conditions. Unintended acceleration or deceleration can increase the risk of a crash.
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NHTSA
26V151000
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Vehicle | High |
Mar 13, 2026
Recall: Mar 13, 2026
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Details |
|
Liftgate Hinge Cover May Detach
Chrysler (FCA US, LLC) is recalling certain 2024-2026 Jeep Wagoneer S vehicles. The liftgate hinge cover may not be properly clipped into position and may detach from the vehicle. A detached hinge cover can become a road hazard for other vehicles, increasing the risk of a crash.
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NHTSA
26V141000
|
Vehicle | High |
Mar 12, 2026
Recall: Mar 12, 2026
|
Details |
|
Loose Handlebar Lock Screw May Detach and Interfere with Steering
Honda (American Honda Motor Co.) is recalling certain 2023-2025 CMX300, CMX500, and CL500 motorcycles. The handlebar lock screw may loosen and detach. A detached screw may lodge between the frame and stem, interfering with steering and increasing the risk of a crash or injury.
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NHTSA
26V146000
|
Vehicle | High |
Mar 12, 2026
Recall: Mar 12, 2026
|
Details |
|
Loose Bolts May Damage Seat Belt Webbing
BMW of North America, LLC (Rolls-Royce) is recalling certain 2020-2026 Rolls-Royce Cullinan vehicles. The fixing bolts may not have been properly tightened. The bolts may loosen and damage the left or right rear seat belt webbing or allow the backrest to move under pressure from items in the luggage compartment. A damaged seat belt or unsecured seat back may not adequately restrain the seat occupant, increasing the risk of 135/2,000 Safety Risk: Crash Fire Death Injury Consumer Advisories: Do Not Drive Park Outside Remedy Description:injury during a crash.
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NHTSA
26V143000
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Vehicle | High |
Mar 12, 2026
Recall: Mar 12, 2026
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Details |
Stoney Games Recalls Kluster Magnet Chess Games Due to Risk of Serious Injury or Death from Magnet Ingestion; Violates Mandatory Standard for Toys
This recall involves the Kluster Fun Tabletop Magnet Chess Games with small, loose magnets about .5 to one inch wide and .3 to .4 inches high. The games are sold in a black box with the word "Kluster" on the front of the box. The games include about 24 magnets, an orange string, an instruction manual and a black storage pouch with "Kluster" printed on the front. The games were also sold in a white pouch with gameplay instructions printed on the back.
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CPSC
10656
|
Child/Baby | High |
Mar 12, 2026
Recall: Mar 12, 2026
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Details |
ProRider Recalls Bicycle Helmets Due to Risk of Serious Injury or Death from Head Injury; Violates Mandatory Standard for Bicycle Helmets
This recall involves ProRider Economy, Bike Helmets with turn ring, Bike Helmets Black Foam, BMX Helmet and Toddler Bike Helmets. The helmets were sold in the following colors: blue, green, red, black, and purple. The model number, date of manufacture in MM/YYYY format, and serial number can be found on a label inside the helmet. Model Number Model Name Size(s) Manufacture Date Serial Number(s) BG-W/10BICYCLE Economy Bicycle Helmet S/M (Small/Medium) 12/2022 00158202 and 00158287 L/XL (Large/Xtra-Large) 44652 00094738 and 00094811 BG-14BICYCLE Bike Helmet with turn ring S/M (Small/Medium) 12/2022 00141944 and 00140406 L/XL (Large/Xtra-Large) 44835 00134699 and 00134652 BG-14BICYCLE Bike Helmet Black Foam L/XL (Large/Xtra-Large) 12/2022 145398 SPORT HELMET BMX Helmet XS (Xtra-Small) 09/2022 127689 BM-5TODDLER Toddler Bike Helmet XXS (Xtra-Xtra-Small) 09/2022 None
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CPSC
10657
|
Consumer Product | High |
Mar 12, 2026
Recall: Mar 12, 2026
|
Details |
LIVEHOM 11-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units; Sold on Amazon by Simplehome
This recall involves LIVEHOM-branded 11-Drawer Dressers. The recalled dressers are made of fabric and were sold in black, white, pink, rustic brown and charcoal black. They measure about 11.8 inches long, 39 inches wide and 46 inches tall and have 11 fabric drawers. The brand name can be found on the product sale receipt.
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CPSC
10658
|
Child/Baby | High |
Mar 12, 2026
Recall: Mar 12, 2026
|
Details |
17 Stories Furniture 14-Drawer Dressers Recalled Due to Risk of Serious Injury or Death from Tip-Over and Entrapment Hazards; Violates Mandatory Standard for Clothing Storage Units; Imported by Hong Kong Baojia International
This recall involves 17 Stories Furniture 14-Drawer Dressers. The recalled dressers were sold in the following colors: black, white, and brown. They have 14 fabric drawers and are 11.8 inches long by 37.4 inches wide by 52.2 inches tall. They have a metal frame, wooden top and 14 collapsable fabric drawers. Model numbers 55SCDR14KDBRDL, 55SCDR14KDCHDL, 55SCDR14KDPDL, 55SCDR14KDWPVCDL, and 55SCDR14KDGDL can be found on the product's packaging, or on the order information in your Wayfair account.
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CPSC
10659
|
Child/Baby | High |
Mar 12, 2026
Recall: Mar 12, 2026
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Details |
|
Brand Name: ShockPulse-SE Lithotripsy System SPL-S Product Name: ShockPulse-SE Lithotripsy System - Single Use Probes Model/Catalog Number: SPL-S Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating stone debris. The ShockPulse transducer is a reusable device that requires cleaning and steam sterilization prior to use in order to generate both low-frequency mechanical impacts and high-frequency ultrasonic energy that quickly disintegrates stones.
Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the transducer plug and/or generator receptacle may cause these issues.
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FDA
Z-1478-2026
|
Medical Device | High |
Mar 11, 2026
Recall: Nov 14, 2025
|
Details |
|
Brand Name: HiResolution Bionic Ear System Product Name: Sky CI M90 Sound Processor Model/Catalog Number: CI-5295-150
Behind-the-ear sound processer packaging label is different then included product.
|
FDA
Z-1493-2026
|
Medical Device | High |
Mar 11, 2026
Recall: Nov 27, 2025
|
Details |
|
Brand Name: Olympus ShockPulse-SE Lithotripsy System with Generator Product Name: ShockPulse-SE Lithotripsy System - Reuseable Probes Model/Catalog Number: SPL-SR, contains generator SPL-G Product Description: An assembly of devices that uses a combination of, or individually applied, pneumatically-created ballistic shock waves and ultrasonic waves for the intracorporeal fragmentation of stones (calculi) in the urinary tract (i.e., kidney, ureter, and bladder) for their removal. It typically includes a pressure and power regulator/control unit, handpieces, and two types of probes of various si
Mis-wired component-the improperly wired component can result in additional noise on the power supply output. Noise on the ultrasonic input circuit is not consistent with electromagnetic compatibility (EMC) standards and may decrease the overall reliability of the system and result in delay of treatment. It was discovered that additional serial numbers of ShockPulse generators may also have the mis-wired component. As a result, this is expanding the action to the additional impacted devices.
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FDA
Z-1494-2026
|
Medical Device | High |
Mar 11, 2026
Recall: Jan 8, 2026
|
Details |
|
Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE, 633010PE, 633007PE, 636010PE, 632522PE, 633012PE, 635018PE, 631516PE, 636016PE, 631220PE, 631608PE, 631206PE, 631407P50E, 631508PE, 636008PE, 636006PE, 632518PE, 634008PE, 634006PE, 631218PE, 632211PE, 634007PE, 633006PE, 631506PE, 632524PE, 636007PE, 631512PE, 636012PE, 636014PE, 632211P50E, 633016PE, 631407PE, 631809PE, 632010PE, 631608P50E, 632520PE, 632412PE, 631510PE, 635022PE, 631224PE, 632412P50E, 631507PE, 633014PE, 632010P50E, 635020PE, 631809P50E. Gelweave, REF: 736038E, 736036E, 736034E, 736032ST/10DE, 736032E, 736030ST/10DE
Gelatin sealed woven polyester prostheses devices, designed for vascular repair, were incorrectly labeled with an additional month of shelf life. Device expiry should have been calculated from gel impregnation (date of manufacture) but it was incorrectly calculated from device packaging.
|
FDA
Z-1492-2026
|
Medical Device | High |
Mar 11, 2026
Recall: Dec 18, 2025
|
Details |
|
Brand Name: STA Liatest Free Protein S Product Name: STA Liatest Free Protein S Model/Catalog Number (REF): 00516 Product Description: The STA¿ - Liatest¿ Free Protein S kits are intended for use on STA-R¿ and STA Compact¿ for the quantitative antigenic assay of free protein S in human citrated plasma by the immuno-turbidimetric method. Component: Not Applicable
The potential of out-of-range results and an underestimation of the free protein S level in normal patient plasmas. The defect only affects normal-range values.
|
FDA
Z-1491-2026
|
Medical Device | High |
Mar 11, 2026
Recall: Feb 4, 2026
|
Details |
|
Brand Name: ShockPulse-SE Lithotripsy System SPL-SR Product Name: ShockPulse-SE Lithotripsy System - Reusable Probes Model/Catalog Number: SPL-SR Product Description: The ShockPulse Lithotripsy System is an electromechanical device capable of fragmenting calculi and aspirating stone debris. The ShockPulse transducer is a reusable device that requires cleaning and steam sterilization prior to use in order to generate both low-frequency mechanical impacts and high-frequency ultrasonic energy that quickly disintegrates stones.
Ongoing investigations identified additional instances of the device Generator remaining in a blinking phase waiting to recognize the transducer. Damage to the transducer plug and/or generator receptacle may cause these issues.
|
FDA
Z-1477-2026
|
Medical Device | High |
Mar 11, 2026
Recall: Nov 14, 2025
|
Details |
|
Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Winged INF Model/Catalog Number: 7B3050 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection of air or fluids. Component: N/A
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
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FDA
Z-1481-2026
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Medical Device | High |
Mar 11, 2026
Recall: Feb 2, 2026
|
Details |
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Brand Name: B. Braun Product Name: 21GA WINGED INFUSION, SINGLE PK Model/Catalog Number: 7A3842 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection of air or fluids. Component: N/A
The potential for the needle tip to be dull/blunt, difficult to advance, and/or break.
|
FDA
Z-1482-2026
|
Medical Device | High |
Mar 11, 2026
Recall: Feb 2, 2026
|
Details |
Use the Today filter when you want newly published recall alerts from the current U.S. date. If no results appear, check the last 7 or 10 days because agencies may publish updates in batches.
Recent recalls can include new notices, updated classifications, expanded lots, changed risk levels and public health alerts. Sort by newest first for the live recall feed view.
High-risk notices often involve serious injury, contamination, undeclared allergens, vehicle crash hazards, fire risks or products that should not be used or consumed.
This latest recall page combines CPSC, FDA, USDA FSIS and NHTSA data so shoppers do not need to check each agency page separately.
New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.
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FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.
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Choose food, vehicle, medical device, baby product, electronics, household or consumer product when the latest list is too broad.
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