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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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Recent Product Recall Alerts List

Showing 2,351 - 2,375 of 4,622 matching product recalls.
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Product Recall Source Type Risk Date Action
Philips Azurion 3M12, Model Numbers: 722063, 722221 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.
FDA Z-2284-2026
Medical Device High
Jun 10, 2026 Recall: Dec 7, 2023
Details
Avanta Multi-Patient Administration Tube Sets (AVA 500 MPAT (Part 2 of 2)) used with the Medrad¿ Avanta Injection System; Catalog number: AVA 500 MPAT (Part 2 of 2); Affected material numbers: 87629007, 60729458, 86566648;
Supplier changes resulted in a fit issue with the Contrast Flow Control Valve (CFCV) interface on the Avanta Injector System. Multiple customer reports indicate that the stopcock cannot be reliably engaged with the CFCV snap interface. In instances where engagement is achieved through applied force, the connection is unstable, and the stopcock may disengage before or during contrast injection, leading to procedure interruption.
FDA Z-2296-2026
Medical Device High
Jun 10, 2026 Recall: Apr 24, 2026
Details
BD Pyxis MedBank Tower REF: 1145-00 Medication cabinet
Fingerprint scanner may overheat to a temperature to cause 1st degree burn.
FDA Z-2303-2026
Medical Device High
Jun 10, 2026 Recall: Apr 30, 2026
Details
BD¿Spinal Tray with BD¿Quincke Needle 26 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405632.
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.
FDA Z-2250-2026
Medical Device High
Jun 10, 2026 Recall: Apr 27, 2026
Details
Brand Name: B. BRAUN MEDICAL INC Product Name: CESK NORTHSIDE ANESTHESIA TRAY Model/Catalog Number: 555076 Software Version: N/A Product Description: CESK NORTHSIDE ANESTHESIA TRAY Component: No
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.
FDA Z-2263-2026
Medical Device High
Jun 10, 2026 Recall: Jan 29, 2026
Details
Atlan A350XL. Model Number: 8621600. anesthesia workstation
The Atlan anesthesia workstation either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.
FDA Z-2208-2026
Medical Device High
Jun 10, 2026 Recall: May 7, 2026
Details
FDA Z-2273-2026
Medical Device High
Jun 10, 2026 Recall: Apr 23, 2026
Details
Spinocan Spinal Needle procedure kits: Material Description (Material Number): Spinocan 26 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333201); Spinocan 25 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333211); Spinocan 22 Ga. x 3-1/2 in. (90 mm), Bupivacaine 0.75% with Dextrose 8.25% Tray (Kit) (333231)
These procedure kits contain Bupivacaine Hydrochloride in Dextrose Injection, USP. The manufacturer of the Bupivacaine, Huon Co, Ltd., has issued a voluntary recall due to potential quality issues identified during a recent FDA manufacturing facility inspection.
FDA Z-2277-2026
Medical Device High
Jun 10, 2026 Recall: May 6, 2026
Details
BD¿Spinal Tray with BD¿Whitacre Needle 22 G x 3.5 in.; lidocaine HCL (1%), 5 mL, bupivacaine HCL (0.75%) with dextrose (8.25%), 2 mL (marcaine). Catalog Number: 405645.
This is a sub-recall of a product recall from Huons Co, Ltd., the manufacturer of Bupivacaine Hydrochloride in Dextrose Injection, USP. The recall is due to quality issues identified during an FDA manufacturing facility inspection, citing specific quality deficiencies related to acceptance testing.
FDA Z-2251-2026
Medical Device High
Jun 10, 2026 Recall: Apr 27, 2026
Details
Philips Azurion 3M15, Model Numbers: 722064, 722222 with Software release R2.2.0, R2.2.1, R2.2.3, R2.2.5 and R2.2.6 with the Roadmap Pro Software key
During the device phase of Roadmap Pro, a user may experience a dark image that is not clinically usable. The dark image may result after the user performs a pedal tap (shortly touching the footswitch pedal without generating an Xray image). The pedal tap may cause a dark image with the next fluoroscopy run.
FDA Z-2285-2026
Medical Device High
Jun 10, 2026 Recall: Dec 7, 2023
Details
Brand Name: B. BRAUN MEDICAL INC. Product Name: CESK HARRIS METHODIST Model/Catalog Number: 555498 Software Version: N/A Product Description: CESK HARRIS METHODIST Component: No
B. Braun was notified by our supplier, Ferndale Laboratories, Inc., the manufacturer of MASTISOL¿ Liquid Adhesive, that they have issued a voluntary recall due to potential cracking of the butyrate tubing (outside tube), which renders the product unusable.
FDA Z-2266-2026
Medical Device High
Jun 10, 2026 Recall: Jan 29, 2026
Details
Missing Pedestrian Warning Sounds/FMVSS 141
Denago EV is recalling certain 2024-2025 Nomad, 2024-2026 Nomad XL, 2026 Scout 2, 2026 Scout 4, 2024-2026 Rover XL, 2024-2026 Rover XXL, and 2024-2026 Rover XL6 vehicles. The vehicles may fail to make pedestrian warning sounds when in motion. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 141, "Minimum Sound Requirements for Hybrid and Electric Vehicles." A vehicle that does not emit sound may fail to alert pedestrians of a moving vehicle, increasing the risk of a crash or injury.
NHTSA 26V381000
Vehicle High
Jun 10, 2026 Recall: Jun 10, 2026
Details
Engine Stall From Canister Purge Valve Malfunction
Ford Motor Company (Ford) is recalling certain 2012-2018 Focus vehicles previously repaired incorrectly under recall number 18V735. The Canister Purge Valve (CPV) may malfunction, causing the engine to stall unexpectedly while driving. An engine that stalls while driving increases the risk of a crash.
NHTSA 26V369000
Vehicle High
Jun 9, 2026 Recall: Jun 9, 2026
Details
Instrument Cluster Failure/FMVSS 102
Ford Motor Company (Ford) is recalling certain 2017 F-150 vehicles previously repaired incorrectly under recall number 17V053. The instrument cluster may lose power after initial vehicle start-up in cold ambient temperatures. Several gauges, including the transmission gear position indicator, may not illuminate. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 102, "Transmission Shift Lever Sequence, Starter Interlock, and Transmission Braking Effect." An instrument cluster that fails to display critical safety information, such as gear position or warning lights, increases the risk of a crash or injury.
NHTSA 26V370000
Vehicle High
Jun 9, 2026 Recall: Jun 9, 2026
Details
Vehicle Rollaway Risk
Ford Motor Company (Ford) is recalling certain 2024 Explorer vehicles equipped with a 2.3L engine and 10R60 automatic transmission. An unintentional powertrain control module (PCM) reset may occur while the vehicle is in motion and result in park system damage. A park system that is damaged may not shift into "PARK," resulting in a vehicle rollaway and increasing the risk of injury or crash.
NHTSA 26V371000
Vehicle High
Jun 9, 2026 Recall: Jun 9, 2026
Details
Instrument Cluster May Go Blank on Start-Up/FMVSS 101
Ford Motor Company (Ford) is recalling certain 2019 Ford Mustang, Lincoln Nautilus, and Lincoln Navigator vehicles previously repaired incorrectly under recall number 19V076. At vehicle start-up, the Instrument Panel Cluster Assembly (IPC) may not function, showing a blank display. As a result, these vehicles fail to comply with Federal Motor Vehicle Safety Standard (FMVSS) number 101, "Controls and Displays." A blank instrument cluster that fails to display critical safety information, such as vehicle speed or safety system warnings, increases the risk of a crash.
NHTSA 26V372000
Vehicle High
Jun 9, 2026 Recall: Jun 9, 2026
Details
Daytime Running Lights May Not Dim/FMVSS 108
Ford Motor Company (Ford) is recalling certain 2018-2020 F-150 vehicles previously repaired incorrectly under recall number 20V097. When the headlight switch is turned from "Autolamps" to "Headlamps On," the Daytime Running Lamps (DRLs) may remain fully bright instead of dimming to parking lamps as intended. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 108, "Lamps, Reflective Devices and Associated Equipment." Daytime Running Lamps that do not dim may reduce the visibility of other drivers, increasing the risk of a crash.
NHTSA 26V373000
Vehicle High
Jun 9, 2026 Recall: Jun 9, 2026
Details
Unintended Vehicle Movement
Ford Motor Company (Ford) is recalling certain 2018 F-150 vehicles previously repaired incorrectly under recall number 17V669. Quickly moving the shift lever from Park to Drive may cause a loss of gear indication on the instrument cluster display and a momentary selection of an unintended gear, such as Reverse or Neutral. Unintended gear selection may cause the vehicle to move in an unexpected direction, increasing the risk of crash or injury.
NHTSA 26V375000
Vehicle High
Jun 9, 2026 Recall: Jun 9, 2026
Details
Steering Wheel Hands-Off Detection Alerts May Fail
Ford Motor Company (Ford) is recalling certain 2019 Lincoln Nautilus vehicles previously repaired incorrectly under recall number 19V031. The lane center assist system may not adequately detect if a driver has their hands off the steering wheel for a prolonged period of time. Failure to alert the driver with the intended hands-off the wheel warnings may increase the risk of a crash.
NHTSA 26V377000
Vehicle High
Jun 9, 2026 Recall: Jun 9, 2026
Details
Hydraulic Jack May Extend Unexpectedly
Vermeer Manufacturing Company (Vermeer) is recalling certain 2002-2026 BC1800XL brush chipper trailers. The hydraulic jack may extend unexpectedly. An extended jack may contact the ground while driving, causing a loss of vehicle control and increasing the risk of injury or a crash.
NHTSA 26V379000
Vehicle High
Jun 9, 2026 Recall: Jun 9, 2026
Details
Unexpected Downshift Can Cause Loss of Control
Ford Motor Company (Ford) is recalling certain model year 2014 F-150 vehicles previously repaired incorrectly under recall number 24V444. A loss of signal between the transmission output shaft speed sensor and the powertrain control module (PCM) can cause the transmission to unexpectedly downshift into first gear. Unexpectedly downshifting into first gear may result in a loss of vehicle control, increasing the risk of a crash.
NHTSA 26V378000
Vehicle High
Jun 9, 2026 Recall: Jun 9, 2026
Details
SUNS International Recalls Residential Elevator Interlock Switches Due to Fall and Crushing Hazard; Risk of Death or Serious Injury
SUNS International Recalls Residential Elevator Interlock Switches Due to Fall and Crushing Hazard; Risk of Death or Serious Injury
This recall involves all SUNS International SS6291 Solenoid Interlock switches used in residential elevators produced from August 20, 2024, through November 6, 2025, with date codes 2431 through 2543. The SUNS SS6291 interlock switch measures approximately 10 inches by 2 inches and weighs about 2-pounds. "SUNS", the model number and date code are printed on a label on the side of the product.
CPSC 10804
Consumer Product High
Jun 5, 2026 Recall: Jun 4, 2026
Details
Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Broqixin
Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Broqixin
This recall involves Broqixin-branded pool drain covers. The white plastic pool drain covers measure about 7.36 inches in diameter and weigh about 3.84 ounces and come with two screws. "Model 11064W" is printed on the product's packaging.
CPSC 10802
Consumer Product High
Jun 5, 2026 Recall: Jun 4, 2026
Details
Little Grape Land Recalls Nursing Pillows Due to Risk of Serious Injury or Death from Suffocation; Violate Mandatory Standards for Nursing Pillows and Infant Support Cushions
Little Grape Land Recalls Nursing Pillows Due to Risk of Serious Injury or Death from Suffocation; Violate Mandatory Standards for Nursing Pillows and Infant Support Cushions
This recall involves Little Grape Land Nursing Pillows. The nursing pillows are U-shaped and come in a rose floral, alligator, bear, butterfly, cactus, construction truck, forest deer, green leaves, little bunny, spring flower and woodland animal patterns. There are no markings or labels on the product.
CPSC 10798
Child/Baby High
Jun 5, 2026 Recall: Jun 4, 2026
Details
Crenlux Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Eicong
Crenlux Pool Drain Covers Recalled Due to Risk of Serious Injury or Death from Entrapment and Drowning Hazards; Violates Virginia Graeme Baker Pool & Spa Safety Act; Sold on Amazon by Eicong
This recall involves Crenlux-branded pool drain covers. The white plastic pool drain covers measure about eight inches in diameter and weigh about 12.7 ounces. "Crenlux" is printed on the product's packaging.
CPSC 10800
Consumer Product High
Jun 5, 2026 Recall: Jun 4, 2026
Details
Showing 2,351 - 2,375 of 4,622 product recalls

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CPSC

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