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 |
|---|---|---|---|---|---|
|
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 |
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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.
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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 |
|
Covidien Mon-a-Therm general purpose temperature probe size: 9 Fr REF: 90050
Temperature probe devices lack FDA clearance.
|
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
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
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
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
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 |
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.
Recent FDA notices can include Class I, Class II and Class III recalls, market withdrawals, safety alerts, code information and distribution areas.
FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.
New vehicle, tire, equipment and child-seat campaigns include defect summaries, affected units, remedy notes and NHTSA campaign numbers.
Recent recall pages are date-driven. Use the published date and recall date to understand whether an alert is new, newly classified or recently updated.
Choose food, vehicle, medical device, baby product, electronics, household or consumer product when the latest list is too broad.
Sort by highest risk when checking for urgent problems such as contamination, serious injury hazards, undeclared allergens, fire risks or vehicle safety defects.
Use the detail page and official source link before taking action. Agency notices may include exact lot codes, model ranges, remedy steps and company contacts.
The site syncs official recall sources daily and stores updated records by source agency, dataset and official recall ID.
Some agencies publish or classify a recall after the company began the recall. Use both the published date and recall date when reviewing a notice.
Match the brand, product name, package size, UPC, lot code, best-by date, allergen or contamination issue and distribution area before taking action.
Yes. Use the risk filter or highest-risk sort to surface recalls marked critical or high risk across all official sources.