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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Medline Convenience Kits: 1) BASIC NERVE BLOCK TRAY W/LINEN, Model Number:PAIN0150C
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
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FDA
Z-2116-2026
|
Medical Device | High |
May 13, 2026
Recall: Jan 7, 2026
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Details |
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LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219, 99577-001957, 99577-001935, 99577-001964, 99577-001955, 99577-001956, 99577-001588, 99577-001958, 99577-001950, 99577-001962, 99577-002178, 99577-001372, 99577-001938, 99577-000045; LIFEPAK 1000, REF: 99425-000025, 99425-000023, 99425-000096; LIFEPAK 35, REF: 99335-000013, 99335-000031; LIFEPAK 20e, REF: 99507-000122
Some defibrillators serviced between July 2023 through November 2025 were serviced without objective evidence that a Performance Inspection Procedure (PIP) was conducted, and the inability to perform the device's intended use may result in potential harms such as delays or inability to provide therapy.
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FDA
Z-2065-2026
|
Medical Device | High |
May 13, 2026
Recall: Apr 13, 2026
|
Details |
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See RES for complete list. Medline Convenience Kits: 1) OPEN HEART CDS, Model Number:CDS840015AQ; 2) OPEN HEART CDS, Model Number:CDS840015AQ; 3) OPEN HEART CDS, Model Number:CDS840023T; 4) OFF PUMP CABG CDS, Model Number:CDS840087AI; 5) OFF PUMP CABG CDS, Model Number:CDS840087AK; 6) OFF PUMP CABG CDS, Model Number:CDS840087AL; 7) OFF PUMP CABG CDS, Model Number:CDS840087AM; 8) OPEN HEART, Model Number:CDS840150S; 9) OPEN HEART, Model Number:CDS840150T;
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
|
FDA
Z-2093-2026
|
Medical Device | High |
May 13, 2026
Recall: Jan 7, 2026
|
Details |
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Prodisc C SK U.S. IMPLANT EXTRA LARGE 5MM. Model: PDSXL5 Total cervical disc replacement.
Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was labeled as a 6mm.
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FDA
Z-2050-2026
|
Medical Device | High |
May 13, 2026
Recall: Mar 20, 2026
|
Details |
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Medline Convenience Kits: 1) LITHOTOMY PACK, Model Number: DYNJ83185; 2) LITHOTOMY PACK, Model Number: DYNJ83185A; 3) LAP BASIN, Model Number: DYNJVB91109D
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
|
FDA
Z-2100-2026
|
Medical Device | High |
May 13, 2026
Recall: Jan 7, 2026
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Details |
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One Step K in vitro diagnostic test REF: 81A4
The devices were distributed without required FDA premarket clearance or approval.
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FDA
Z-2087-2026
|
Medical Device | High |
May 13, 2026
Recall: Apr 2, 2026
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Details |
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Medline Convenience Kits: 1) PPE KIT, Model Number: DYK1011945P
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
|
FDA
Z-2104-2026
|
Medical Device | High |
May 13, 2026
Recall: Jan 7, 2026
|
Details |
|
Medline Convenience Kits: 1) WMC I D PACK-LF, Model Number: DYNJ50806L
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
|
FDA
Z-2119-2026
|
Medical Device | High |
May 13, 2026
Recall: Jan 7, 2026
|
Details |
|
Halyard CARDIAC CATH TRAY SHANDS JAX kit. Model Number: SHND401-04, SHND401-05.
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
|
FDA
Z-1972-2026
|
Medical Device | High |
May 13, 2026
Recall: Mar 13, 2026
|
Details |
|
See RES for complete list. Medline Convenience Kits: 1) PLASTIC BIN W/MISC KITS, Model Number: ACC010499; 2) BREAST-HERNIA-PORT CDS-LF, Model Number: CDS984853J; 3) KIT UROLOGY URETHROPLASTY, Model Number: DYKMBNDL117C; 4) KIT PLASTIC INSERT TISSUE EXPA, Model Number: DYKMBNDL158; 5) KIT PLASTIC ABDOMINOPLASTY, Model Number: DYKMBNDL170; 6) KIT PLASTIC ABDOMINOPLASTY, Model Number: DYKMBNDL170A; 7) KIT PLASTIC ABDOMINOPLASTY, Model Number: DYKMBNDL170B; 8) KIT PLASTIC ABDOMINOPLASTY, Model Number: DYKMBNDL182;
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packaging cycles; however, the identified calibration issues have the potential to impact the sterility assurance level (SAL) of the Recalled Products.
|
FDA
Z-2099-2026
|
Medical Device | High |
May 13, 2026
Recall: Jan 7, 2026
|
Details |
|
Touch Screen Display May Fail
Hale Products Inc (Hale) is recalling certain Weldon UV800 Display Unit user interfaces, with part numbers 610-00060-080-51, 610-00060-080-50, 610-00060-081, and 610-00091. The display may stop responding to touch commands or fail to power on, preventing the activation of exterior emergency lights, fire fighting and other emergency equipment. A loss of exterior lights can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash. Inoperative equipment can delay emergency response, increasing the risk of injury.
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NHTSA
26E030000
|
Vehicle | High |
May 13, 2026
Recall: May 13, 2026
|
Details |
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Inverter May Fail and Cause a Loss of Drive Power
Lucid USA, Inc. (Lucid) is recalling certain 2024-2025 Air vehicles equipped with rear-wheel drive. The Gen 4 inverter may experience internal friction and become damaged, causing a loss of drive power. A loss of drive power increases the risk of a crash.
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NHTSA
26V309000
|
Vehicle | High |
May 13, 2026
Recall: May 13, 2026
|
Details |
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Seat Belt Warning System Malfunction/FMVSS 208
Jaguar Land Rover North America LLC (Land Rover) is recalling certain 2026 Land Rover Range Rover Velar, Range Rover Sport, and Range Rover vehicles. The seat belt warning system may not activate the audible warning chime as intended. As such, these vehicles fail to conform with the requirements of Federal Motor Vehicle Safety Standard number 208, "Occupant Crash Protection." A seat belt chime that fails to alert occupants that they are unbuckled can increase the risk of injury during a crash.
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NHTSA
26V297000
|
Vehicle | High |
May 12, 2026
Recall: May 12, 2026
|
Details |
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Hard Top May Crack and Detach
Ford Motor Company (Ford) is recalling certain 2021-2022 Bronco vehicles. The 3-door and 5-door Molded-In-Color (MIC) hardtop roof panels may have been manufactured improperly, which can allow sections of the outer roof panel to separate and detach from the vehicle. A detached section of roof can create a road hazard, increasing the risk of a crash.
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NHTSA
26V299000
|
Vehicle | High |
May 12, 2026
Recall: May 12, 2026
|
Details |
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DOT Code Mark Missing from Driver's Door Window/FMVSS 205
Nova Bus (US) Inc. (Nova Bus) is recalling certain 2019-2020 LFS Artic and 2019-2023 LFS transit buses. The driver's speaker hole door may have been built with the prime glazing manufacturer DOT code mark missing. As such, these vehicles fail to conform to Federal Motor Vehicle Safety Standard (FMVSS) number 205, "Glazing Materials." A missing DOT code mark may result in the door being replaced with the incorrect type of plastic, reducing visibility and increasing the risk of a crash.
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NHTSA
26V300000
|
Vehicle | High |
May 12, 2026
Recall: May 12, 2026
|
Details |
|
Vehicle Rollaway Risk/FMVSS 114
Ford Motor Company (Ford) is recalling certain 2026 Escape and Lincoln Corsair vehicles. The integrated park module may fail to lock into the park position when the driver shifts into park. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 114, "Theft Protection and Rollaway Prevention." A loss of park function can allow the vehicle to rollaway, increasing the risk of a crash.
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NHTSA
26V301000
|
Vehicle | High |
May 12, 2026
Recall: May 12, 2026
|
Details |
|
Missing Warning on Rearview Mirrors
Piaggio Group Americas, Inc. (PGA) is recalling certain 2026 Vespa GTV 310, Vespa Primavera 150, and Vespa Primavera 50 motorcycles in the color Officina 8. The convex mirror warning "objects in mirror are closer than they appear," is missing. Without the convex mirror warning, riders may misjudge the distance of other vehicles, resulting in unsafe lane changes or maneuvers, increasing the risk of a crash.
|
NHTSA
26V302000
|
Vehicle | High |
May 12, 2026
Recall: May 12, 2026
|
Details |
|
Delayed Service Brake Release/FMVSS 121
International Motors, LLC (International) is recalling certain 2026-2027 HV vehicles. The service brake may take longer than expected to release. As such, these vehicles may fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 121, "Air Brake Systems." A delayed brake release can increase the risk of crash.
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NHTSA
26V294000
|
Vehicle | High |
May 11, 2026
Recall: May 11, 2026
|
Details |
|
Improperly Tightened Lower Ball Joint Nut
Federal-Mogul Motorparts LLC (DRiV) is recalling certain Beck/Arnley replacement lower control arm and ball joint assemblies for 2018-2025 Subaru Forester and Crosstrek vehicles. The lower ball joint nut may be loose or may not have been tightened properly. A loose nut may allow the ball joint to separate from the control arm, causing a loss of steering control and increasing the risk of a crash.
|
NHTSA
26E028000
|
Vehicle | High |
May 11, 2026
Recall: May 11, 2026
|
Details |
|
Unintended Brake Light Illumination/FMVSS 108
Shyft Group (Shyft) is recalling certain 2025 Spartan RV Chassis K1, 2024-2026 RV Chassis K2, RV Chassis K3, and 2025-2027 RV Chassis K4 vehicles. The exterior brake lights may remain illuminated when the driver is not applying the brakes. 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." Brake lights that remain on may fail to alert other vehicles of the driver's intention, increasing the risk of a crash.
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NHTSA
26V292000
|
Vehicle | High |
May 8, 2026
Recall: May 8, 2026
|
Details |
|
Brakes May Not Function Properly/FMVSS 122
Taizhou Qianxin Vehicle Co. Ltd is recalling certain 2024 Fly Wing Snake 250 EFI motorcycles. The brake pads may fail to stop the motorcycle as intended in wet road conditions. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 122, “Motorcycle Brake Systems.” The braking performance in wet road conditions may be reduced, resulting in extended braking distance, increasing the risk of a crash.
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NHTSA
26V293000
|
Vehicle | High |
May 8, 2026
Recall: May 8, 2026
|
Details |
|
Vent Fan Lid May Detach in Transit
Dometic Corporation (Dometic) is recalling certain Fan-Tastic Vent Fans with part numbers 9610007185, 9610007184, 9610007183, 9610007182, 9610007181, and 9610007180. The vent fan assembly may be missing a hinge pin, allowing the lid to detach. A detached lid can become a road hazard for other vehicles, increasing the risk of a crash.
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NHTSA
26E027000
|
Vehicle | High |
May 8, 2026
Recall: May 8, 2026
|
Details |
|
Vehicle Can Exceed the Speed Rating of the Tires
Chryser (FCA US LLC) is recalling certain 2023-2026 Ram 2500 Pick up trucks. A software error in the powertrain control module may improperly allow the vehicle speed to exceed the tire speed rating, which can result in a loss of vehicle control. Loss of vehicle control increases the risk of a crash.
|
NHTSA
26V288000
|
Vehicle | High |
May 7, 2026
Recall: May 7, 2026
|
Details |
|
Power Transfer Unit May Fail and Cause a Loss of Drive Power
Chrysler (FCA US LLC) is recalling certain 2019-2023 Jeep Cherokee vehicles. The power transfer unit (PTU) may fail. A failed PTU may result in a loss of drive power or vehicle rollaway, increasing the risk of a crash or injury.
|
NHTSA
26V290000
|
Vehicle | High |
May 7, 2026
Recall: May 7, 2026
|
Details |
ZMC Group Recalls Multiple Light Up Toys Due to Risk of Serious Injury or Death from Battery Ingestion; Violate Mandatory Standard for Toys
This recall involves various ZMC Group battery-operated toys, including: Product Name Item # 19.4" Assorted Colors Light Up Stick 885S-01/02 Light Up Halloween Wands 777-HW Light Up Halo Flower Headband G06-2L Light Up Devil Horns Headband G03-C Light Up Polka Dot Bow Headband G01-1 LED Light Up Flying Disc UFO Lite-Up Maraca 668-23 Light Up Yo-Yo 9987B Cardpack Flashing Whistle Necklace ZS166 Packaging for the products has a label with the item number, identification of the distributor, place of manufacture, production date and batch number. The recall includes all batch numbers for the referenced products.
|
CPSC
10757
|
Child/Baby | High |
May 7, 2026
Recall: May 7, 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.