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Latest Product Recalls Today

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.

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Search recent recall notices by product name, brand, UPC, lot code, model number, source agency or official recall number.

Recent Product Recall Alerts List

Showing 1,676 - 1,700 of 3,321 matching product recalls.
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Product Recall Source Type Risk Date Action
Cpzzkq Baby Loungers Recalled Due to Risk of Serious Injury or Death from Suffocation Hazard; Violates Mandatory Standard for Infant Support Cushions; Sold on Amazon by CetoPMax
Cpzzkq Baby Loungers Recalled Due to Risk of Serious Injury or Death from Suffocation Hazard; Violates Mandatory Standard for Infant Support Cushions; Sold on Amazon by CetoPMax
This recall involves Cpzzkq baby loungers. The baby loungers come in white, grayish blue, pink, zuma blue and brown. The recalled baby loungers are rectangular in shape and are made of a foam pad with a cloth cover. The loungers have the brand printed on a tag on the side of the lounger.
CPSC 10739
Child/Baby High
Apr 24, 2026 Recall: Apr 23, 2026
Details
Children's Tower Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by TOETOL HOME
Children's Tower Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by TOETOL HOME
This recall involves TOETOL HOME-branded children's tower stools, model DETD0001. The wooden kitchen tower step stools were sold in white, gray and dark wood colors and measure about 20 inches deep, 15 inches wide and 36 inches tall with model DETD0001 printed on a label on the side.
CPSC 10733
Child/Baby High
Apr 24, 2026 Recall: Apr 23, 2026
Details
Children's Tower Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by AMZCMJ DGD
Children's Tower Stools Recalled Due to Risk of Serious Injury and Death from Entrapment and Fall Hazards; Imported by AMZCMJ DGD
This recall involves AMZCMJ DGD-branded children's tower stools. The wooden kitchen stools measure about 15 inches deep, 22 inches wide and 34 inches tall. They are foldable and convert into a table and a chair and have a blackboard. The brand name is printed on the product's order receipt.
CPSC 10734
Child/Baby High
Apr 24, 2026 Recall: Apr 23, 2026
Details
Autobrush Recalls Sonic Pro Children's Toothbrush Boxes Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries
Autobrush Recalls Sonic Pro Children's Toothbrush Boxes Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Consumer Products with Coin Batteries
This recall involves Autobrush's Sonic Pro Kids toothbrush boxes used as packaging for delivering children's toothbrushes. The electric toothbrushes consist of a u-shaped mouthpiece and a plastic base with an animal's face that matches the model's name: Unity the Unicorn, Lenni the Lion, Harley the Hippo and Danny the Dino. The light-up, musical toothbrushes have a built-in timer and three brush settings and were sold with a USB cable, a magnetic plug and decoration stickers inside a cardboard delivery box. The delivery box's white tray has a speaker with a coin cell battery on the underside. Additionally, "autobrush KIDS," the toothbrush's model name and an animal image that corresponds to the model are printed on the box.
CPSC 10735
Child/Baby High
Apr 24, 2026 Recall: Apr 23, 2026
Details
32 Degrees Recalls Heated Socks Due to Burn Hazard
32 Degrees Recalls Heated Socks Due to Burn Hazard
This recall involves heated socks sold in three sizes (medium, large, extra large), all in the color black. "32° HEAT" appears on the battery pack casing, battery pack packaging, user manual and the exterior retail packaging for the products.
CPSC 10736
Consumer Product Medium
Apr 24, 2026 Recall: Apr 23, 2026
Details
Rear Brake Modulators May Short Circuit
Volvo Trucks North America (Volvo Trucks) is recalling certain 2026-2027 VNR (4) and 2025-2027 VNL (4) vehicles. The rear brake modulators may have unprotected electrical connectors that can short circuit and lead to a loss of the anti-lock brake system (ABS) and electronic stability control (ESC). A loss of anti-lock brakes and electronic stability control increases the risk of a crash or injury.
NHTSA 26V260000
Vehicle High
Apr 23, 2026 Recall: Apr 23, 2026
Details
Rear Brake Modulators May Short Circuit
Mack Trucks, Inc. (Mack) is recalling certain 2025-2027 Pioneer (4) and 2026-2027 Anthem (4) vehicles. The rear brake modulators may have unprotected electrical connectors that can short circuit and lead to a loss of the anti-lock brake system (ABS) and electronic stability control (ESC). A loss of anti-lock brakes and electronic stability control increases the risk of a crash or injury.
NHTSA 26V261000
Vehicle High
Apr 23, 2026 Recall: Apr 23, 2026
Details
Instrument Panel Display Failure/FMVSS 108, 208
Chrysler (FCA US, LLC) is recalling certain 2024-2025 Jeep Wagoneer S and Dodge Charger electric vehicles. A software error may cause the instrument panel display to fail. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard numbers 108, "Lamps, Reflective Devices, and Associated Equipment," 126, "Electronic Stability Control Systems for Light Vehicles," 135, "Light Vehicle Brake Systems," 138, "Tire Pressure Monitoring System," and/or 208, "Occupant Crash Protection." An instrument panel display that fails to show critical safety information, such as gear selection and warning lights, increases the risk of a crash.
NHTSA 26V262000
Vehicle High
Apr 23, 2026 Recall: Apr 23, 2026
Details
Sediment in Brake Fluid/FMVSS 116
General Motors (GM) is recalling certain containers of ACDelco GMW DOT 3 brake and clutch fluid (lot #01977 091222). The brake fluid may contain visible sediment. As such, this brake fluid fails to conform to Federal Motor Vehicle Safety Standard number 116, "Motor Vehicle Brake Fluids." Sediment in brake fluid may reduce brake performance, increasing the risk of a crash.
NHTSA 26E025000
Vehicle High
Apr 23, 2026 Recall: Apr 23, 2026
Details
Fuel Tank May Leak
Jaguar Land Rover North America, LLC (Land Rover) is recalling certain 2026 Land Rover Defender vehicles. The fuel tank was improperly manufactured with walls that are too thin. In the event of a crash, an improperly manufactured fuel tank may leak fuel, increasing the risk of a fire.
NHTSA 26V263000
Vehicle High
Apr 23, 2026 Recall: Apr 23, 2026
Details
Park Outside: Generator May Turn On Unexpectedly
REV Recreation Group (REV) is recalling certain 2026 Holiday Rambler Vacationer, Admiral, Fleetwood Flair, Fortis, and Bounder motorhomes. The furnace may create electrical signal that turns the generator on unexpectedly. A generator that operates in an enclosed space, such as a garage, increases the risk of injury or death from carbon monoxide poisoning.
NHTSA 26V264000
Vehicle High
Apr 23, 2026 Recall: Apr 23, 2026
Details
FDA H-0681-2026
Food High
Apr 22, 2026 Recall: Apr 1, 2026
Details
FDA H-0664-2026
Food High
Apr 22, 2026 Recall: Mar 20, 2026
Details
FDA H-0665-2026
Food High
Apr 22, 2026 Recall: Mar 23, 2026
Details
B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG. Model Number: SL-2010M2096
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
FDA Z-1799-2026
Medical Device High
Apr 22, 2026 Recall: Mar 19, 2026
Details
B. Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 2.6MM PUMP SEGMENT. Model Number: B3-3632M3705.
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
FDA Z-1802-2026
Medical Device High
Apr 22, 2026 Recall: Mar 19, 2026
Details
Cytal Wound Matrix 2-Layer 10x15 cm. Product ID: WSM1015.
Increased rate of out-of-specification endotoxin results.
FDA Z-1818-2026
Medical Device High
Apr 22, 2026 Recall: Mar 19, 2026
Details
Cytal Wound Matrix 2-Layer 7x10 cm. Product ID: WSM0710.
Increased rate of out-of-specification endotoxin results.
FDA Z-1817-2026
Medical Device High
Apr 22, 2026 Recall: Mar 19, 2026
Details
B Braun Hemodialysis Bloodlines, LOW VOL, NO CHAMBER 4.8MM PUMP SEGMENT. Model Number: B3-4630M4705.
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
FDA Z-1803-2026
Medical Device High
Apr 22, 2026 Recall: Mar 19, 2026
Details
LinkBio CORE Workstation, a component of the CORE Shoulder System. Product Code: 87-9136.
The CORE Workstation may display an incorrect "Planning Date " when viewing cases on the "Start Case" menu screen.
FDA Z-1810-2026
Medical Device High
Apr 22, 2026 Recall: Mar 12, 2026
Details
Cytal Burn Matrix 7x10 cm. Product ID: BMM0710.
Increased rate of out-of-specification endotoxin results.
FDA Z-1819-2026
Medical Device High
Apr 22, 2026 Recall: Mar 19, 2026
Details
B. Braun Hemodialysis Bloodlines, STREAMLINE FRESENIUS FOR DAVITA. Model Number: SL-2000M2095DA.
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
FDA Z-1800-2026
Medical Device High
Apr 22, 2026 Recall: Mar 19, 2026
Details
B. Braun Hemodialysis Bloodlines, STREAMLINE BLOODLINE SET FOR DIALOG DR. Model Number: SL-2010M2096A.
Potential for the accumulation of small air bubbles in the arterial line due to adherence of blood gases to the tubing under negative pressure.
FDA Z-1798-2026
Medical Device High
Apr 22, 2026 Recall: Mar 19, 2026
Details
CENTURION Circumcision Kit, Medline Kit Number/SKU CIT7050F
On lot of Sterile Circumcision Kits was distributed without the required sterilization process and is therefore not sterile.
FDA Z-1824-2026
Medical Device High
Apr 22, 2026 Recall: Mar 16, 2026
Details
ARTIS Pheno VE30A and VE40A, Model 10849000
During 3D acquisitions, lighter and darker patient images may be captured, which may result in less accurate 3D reconstruction. The variation of brightness is a result of a constant unregulated medium dose and the angular change of patient diameter caused by rotational acquisition. This may result in unintentional low-dose radiation exposure to a patient.
FDA Z-1814-2026
Medical Device High
Apr 22, 2026 Recall: Mar 12, 2026
Details
Showing 1,676 - 1,700 of 3,321 product recalls

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CPSC

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FDA

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USDA FSIS

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NHTSA

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