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 |
|---|---|---|---|---|---|
|
Alphenix Models INFX-8000C INFX-8000F INFX-8000V This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicated for use in diagnostic and angiographic procedures for blood vessels in the heart, brain, abdomen and lower extremities.
Due to the fixing screws of ceiling movement gear in ceiling suspended arm that are part of the X-ray interventional systems may become loose.
|
FDA
Z-3014-2026
|
Medical Device | High |
Sep 2, 2026
Recall: Aug 4, 2026
|
Details |
|
Merge PACS and Merge OrthoPACS, medical imaging diagnostic workstation
Software issue may cause measurements to be displayed inaccurately.
|
FDA
Z-3004-2026
|
Medical Device | High |
Sep 2, 2026
Recall: Jul 22, 2026
|
Details |
|
Fresenius Medical Care, 2008T BlueStar Hemodialysis Machine, Model Numbers: 191126, 191130.
Fresenius Medical Care Renal Therapies Group, LLC (FMCRTG) has received complaints regarding flow-, no water-, or temperature-related alarms with the 2008T¿ BlueStar Hemodialysis machines.
|
FDA
Z-3017-2026
|
Medical Device | High |
Sep 2, 2026
Recall: Jun 30, 2026
|
Details |
|
POWERSEAL 5 MM (in diameter) 23 CM (long), Curved Jaw Sealer & Divider, Double Action. GEI / Electrosurgical, cutting & coagulation & accessories
Potential labeling deficiency in which an outer shelf box is incorrectly labeled as a 37-cm device.
|
FDA
Z-3035-2026
|
Medical Device | High |
Sep 2, 2026
Recall: Aug 18, 2026
|
Details |
|
Medline convenience kits labeled as: 1) C-SECTION, Medline Kit SKU DYNJ904612L; 2) C-SECTION, Medline Kit SKU DYNJ911755; 3) AHR C-SECTION KIT, Medline Kit SKU DYNJ912014.
Kits contain a potentially contaminated component which were recalled by the manufacturer
|
FDA
Z-3026-2026
|
Medical Device | High |
Sep 2, 2026
Recall: Jul 10, 2026
|
Details |
|
ORT300, operating room table, ORT300 Modular Table Main Unit Assy Part Numbers 114093-000 and 114093-600
The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked state. This may pose a risk of injury to the patient if unintended rotational movement occurs during a procedure.
|
FDA
Z-3034-2026
|
Medical Device | High |
Sep 2, 2026
Recall: Aug 6, 2026
|
Details |
|
Medline breathing circuits labeled as: 1) HUDSON RCI, CIRCUIT, HTD, DL, NEONATE, 48, Medline Product Number/SKU HUD78007 (Teleflex Product Number/SKU 780-07); 2) HUDSON RCI, DBM-CIRCUIT,VENT,NEONATAL,21 V, Medline Product Number/SKU HUD78009 (Teleflex Product Number/SKU 780-09); 3) HUDSON RCI, DBD-CIRCUIT,VENT,INSIRATORY,HEATED,NEO,4, Medline Product Number/SKU 780-13 (Teleflex Product Number/SKU 780-13); 4) HUDSON RCI, DBD-CIRCUIT,VENT,INSIRATORY,HEATED,NEO,4, Medline Product Number/SKU 780-14 (Teleflex Product Number/SKU 780-14); 5) HUDSON RCI, DBD-CIRCUIT, HTD, DUAL LIMB, NEONATE, Medline P
Neonatal and infant heated wire breathing circuits may experience sporadic failure. The heated wire connector (pigtail) at the humidifier may exhibit discoloration, melting, smoke, burning odor, or other signs of localized thermal damage. Device failure may predispose infant to bronchospasm, inspissated secretions, and airway obstruction, as well as inadvertent positive end-expiratory pressure (PEEP), circuit obstruction, or accidental lavage of pooled fluid into the airway, elevated oxygen consumption, and worsening respiratory distress.
|
FDA
Z-2992-2026
|
Medical Device | High |
Sep 2, 2026
Recall: Jul 13, 2026
|
Details |
|
ORT200, operating room table, including the ORT200 Covered Table Assembly, Reconditioned, Part Number 113821-600 and the ORT200 50/60Hz Covered Table Assy V2 Part Number 114148-000
The linear actuator and rotational lock mechanism components may experience a mechanical failure that prevents the system from transitioning between locked and unlocked state. This may pose a risk of injury to the patient if unintended rotational movement occurs during a procedure.
|
FDA
Z-3033-2026
|
Medical Device | High |
Sep 2, 2026
Recall: Aug 6, 2026
|
Details |
|
Medline convenience kits labeled as: 1) MAJOR PROCEDURE, Medline Kit SKU CDS982040U; 2) OPERATIVE LAP P&S SURGICAL, Medline Kit SKU DYNJ89608; 3) LAPAROSCOPY, Medline Kit SKU DYNJ903479L; 4) LAPAROSCOPY, Medline Kit SKU DYNJ903479M.
Kits contain a potentially contaminated component which were recalled by the manufacturer
|
FDA
Z-3022-2026
|
Medical Device | High |
Sep 2, 2026
Recall: Jul 10, 2026
|
Details |
|
Medline convenience kits labeled as: 1) CMH LITHO MINOR PACK-LF, Medline Kit SKU DYNJ54362F; 2) EAST MAJOR LITHOTOMY, Medline Kit SKU DYNJ900957C; 3) GYN LAPAROTOMY, Medline Kit SKU DYNJ906804B; 4) UNIVERSAL GYN, Medline Kit SKU DYNJ910195A.
Kits contain a potentially contaminated component which were recalled by the manufacturer
|
FDA
Z-3028-2026
|
Medical Device | High |
Sep 2, 2026
Recall: Jul 10, 2026
|
Details |
|
Medline convenience kits labeled as: 1) LAMI FUSION, Medline Kit SKU CDS982035Y; 2) NON MB MJR NEURO CRANI SM PK, Medline Kit SKU DYNJT6104; 3) CRANIOTOMY, Medline Kit SKU DYNJ903471I; 4) KIT CRANIOTOMY RFD, Medline Kit SKU DYNJ906496K.
Kits contain a potentially contaminated component which were recalled by the manufacturer
|
FDA
Z-3029-2026
|
Medical Device | High |
Sep 2, 2026
Recall: Jul 10, 2026
|
Details |
|
Tire Pressure Monitor System May Fail/FMVSS 138
Chrysler (FCA US LLC) is recalling certain 2024-2025 Jeep Wagoneer, 2024-2026 Jeep Grand Cherokee, Jeep Grand Cherokee L, Jeep Grand Cherokee 4XE, Jeep Grand Wagoneer, 2025 Jeep Wagoneer L, 2025-2026 Jeep Grand Wagoneer L, 2026 Jeep Cherokee, and Jeep Grand Wagoneer L PHEV vehicles. Due to a software error, the tire pressure monitoring system may fail to detect low tire pressure and/or fail to illuminate the tire pressure monitoring system (TPMS) warning light as intended. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 138, "Tire Pressure Monitoring System." A TPMS warning light that fails to notify the driver of low tire pressure increases the risk of a crash.
|
NHTSA
26V559000
|
Vehicle | High |
Sep 1, 2026
Recall: Sep 1, 2026
|
Details |
|
Rear Coil Springs May Detach
Chrysler (FCA US, LLC) is recalling certain 2021-2023 Jeep Grand Cherokee L, 2022-2023 Jeep Grand Cherokee, and Jeep Grand Cherokee 4XE vehicles. The rear coil springs may be incorrectly installed and detach from the vehicle while driving. Rear coil springs that detach from the vehicle while driving increase the risk of a crash.
|
NHTSA
26V562000
|
Vehicle | High |
Sep 1, 2026
Recall: Sep 1, 2026
|
Details |
|
Delayed Brake Timing/FMVSS 121
PACCAR Incorporated (PACCAR) is recalling certain 2027 Peterbilt 548 trucks. The front brake valve and hoses may be the incorrect size, which can delay the rear service brake application and release, as well as the trailer gladhand application times. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 121, "Air Brake Systems." Delayed brake response time can increase the risk of a crash.
|
NHTSA
26V567000
|
Vehicle | High |
Sep 1, 2026
Recall: Sep 1, 2026
|
Details |
|
Rearview Camera Image May Not Display/FMVSS 111
Chrysler (FCA US, LLC) is recalling certain 2025-2026 Ram 1500 vehicles. A radio software error may cause the rearview camera image not to display. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 111, "Rear Visibility." A rearview image that does not display reduces the driver's view behind the vehicle, increasing the risk of a crash.
|
NHTSA
26V560000
|
Vehicle | High |
Sep 1, 2026
Recall: Sep 1, 2026
|
Details |
|
Loss of Electronic Stability Control/FMVSS 126
Chrysler (FCA US, LLC) is recalling certain 2025-2026 Chrysler Voyager, Chrysler Pacifica, and 2026 Chrysler Voyager Plug-In Hybrid Electric (PHEV) vehicles. The brake pedal position sensor capacitor may be cracked, which can cause a loss of electronic stability control. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 126, "Electronic Stability Control Systems." A loss of electronic stability control increases the risk of a crash.
|
NHTSA
26V561000
|
Vehicle | High |
Sep 1, 2026
Recall: Sep 1, 2026
|
Details |
|
Incorrectly Installed Furnace May Leak Carbon Monoxide
Forest River, Inc. (Forest River) is recalling certain 2027 Vibe recreational trailers. The furnace exhaust may not be correctly attached to the outside flue, allowing carbon monoxide to buildup inside the passenger cabin. Unvented exhaust fumes increase the risk of injury from carbon monoxide poisoning.
|
NHTSA
26V563000
|
Vehicle | Medium |
Sep 1, 2026
Recall: Sep 1, 2026
|
Details |
|
Light Tower May Detach During Towing
Light Boy America, Inc (Light Boy) is recalling certain 2020 and 2023 Light Boy GBX12SK light towers. The trailer frame may bend at the tow bar, causing the light tower to detach. A detach light tower can become a road hazard for other vehicles, increasing the risk of a crash or injury.
|
NHTSA
26V564000
|
Vehicle | High |
Sep 1, 2026
Recall: Sep 1, 2026
|
Details |
|
Wheelchair Lift May Inadvertently Move
Forest River bus, LLC (Forest River) is recalling certain 2024 Mobility Trans Safetbus, Glaval Universal, 2025 Senator II, and Starcraft Allstar transit buses equipped with certain S-Series and K-Series wheelchair platform lifts. The electrical contactor may fail, preventing the controls from stopping the lift. A wheelchair lift that continues to move while occupied increases the risk of injury.
|
NHTSA
26V565000
|
Vehicle | Medium |
Sep 1, 2026
Recall: Sep 1, 2026
|
Details |
|
Front Suspension Lateral Link May Separate
Tesla, Inc. (Tesla) is recalling certain 2026 Model Y vehicles. One or more front suspension lateral link fasteners may not have been properly tightened, allowing the lateral link to loosen or separate from the sub-frame. A lateral link separation could shift the wheel alignment, causing a loss of vehicle control and increasing the risk of a crash.
|
NHTSA
26V558000
|
Vehicle | High |
Sep 1, 2026
Recall: Sep 1, 2026
|
Details |
|
Propane Tanks May Detach and Missing Remote Shut Off Valve
Tiffin Motorhomes, Inc. (Tiffin) is recalling certain 2026-2027 Wayfarer recreational vehicles. The liquid propane (LP) tank may have been manufactured without the remote shut off and may be loose in the mounting bracket. LP tanks that cannot be shut off increase the risk of a fire. Additionally a loose LP tank may detach and become a road hazard, increasing the risk of a crash.
|
NHTSA
26V557000
|
Vehicle | High |
Aug 31, 2026
Recall: Aug 31, 2026
|
Details |
|
Incorrect Tire Size on Certification Label/FMVSS 120
Jayco, Inc. (Jayco) is recalling certain 2026-2027 Entegra Accolade, Accolade XL, Jayco Seneca, and Seneca Prestige recreational vehicles. The tire size may be incorrect on the vehicle certification label. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 120, "Wheels and Rims-Other than Passenger Cars." Incorrect information may result in the wrong sized replacement tires being installed, increasing the risk of a crash.
|
NHTSA
26V554000
|
Vehicle | High |
Aug 31, 2026
Recall: Aug 31, 2026
|
Details |
|
False Taillight Warning Light on Instrument Panel Display/FMVSS 101
Jayco, Inc. (Jayco) is recalling certain 2027 Entegra Qwest and Jayco Melbourne Prestige recreational vehicles. The taillight harness may have been manufactured with an incorrect resistor. The defective harness may cause the warning light to illuminate on the instrument panel display when the taillights are functioning correctly. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 101, "Control and Displays." The incorrect warning light may fail to alert the driver to critical safety information or cause confusion, increasing the risk of a crash.
|
NHTSA
26V555000
|
Vehicle | High |
Aug 31, 2026
Recall: Aug 31, 2026
|
Details |
|
Wheelchair Lift May Inadvertently Move
Blue Bird Body Company (Blue Bird) is recalling certain 2025-2027 Vision school buses equipped with Ricon K-Series wheelchair platform lifts. The electrical contactor may fail, preventing the controls from stopping the lift. A wheelchair lift that continues to move while occupied increases the risk of injury.
|
NHTSA
26V556000
|
Vehicle | Medium |
Aug 31, 2026
Recall: Aug 31, 2026
|
Details |
|
Weld Failure May Allow Winch to Detach
Magic Tilt Trailers, Inc. (Magic Tilt) is recalling certain 2025-2026 aluminum personal watercraft boat trailers. The weld between the winch and base plate may fail, causing the winch to separate from the mount. A detached winch may increase the risk of injury to people near the trailer.
|
NHTSA
26V553000
|
Vehicle | Medium |
Aug 28, 2026
Recall: Aug 28, 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.