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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 601 - 625 of 4,975 matching product recalls.
Product Recall Search
Product Recall Source Type Risk Date Action
FDA Z-3328-2026
Medical Device High
Oct 7, 2026 Recall: Jul 17, 2026
Details
FDA Z-3297-2026
Medical Device High
Oct 7, 2026 Recall: Aug 18, 2026
Details
FDA Z-0018-2027
Medical Device High
Oct 7, 2026 Recall: Aug 24, 2026
Details
MR 7700; Model number (REF): 1. 782120, 2. 782153, 3. 782155, 4. 782199; Software Versions: R11, R12 and R13;
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.
FDA Z-3313-2026
Medical Device High
Oct 7, 2026 Recall: Aug 28, 2026
Details
FDA Z-0060-2027
Medical Device High
Oct 7, 2026 Recall: Aug 24, 2026
Details
Intrapulmonary Percussive Ventilation, IPV HC, Product Number: S00009; Phasitron, P5-HC
Labeling updated warning not to use Intrapulmonary percussive ventilation (IPV) in conjunction with volatile anesthetic delivery systems because IPV may alter controlled delivery of volatile anesthetic agents, resulting in deeper/lighter anesthetic effects that may result in hypertonia/hypotonia, tachycardia/ bradycardia, elevated intracranial pressure, awareness during anesthesia, oversedation
FDA Z-3325-2026
Medical Device High
Oct 7, 2026 Recall: Aug 18, 2026
Details
Computed Tomography X-ray System, Model: uCT 530 with software
Positron emission tomography and computed tomography x-ray systems have a software problem when Split or Local function is enabled, and multiple RIS exams are merged into a single study, that prevents patient images from being visible on the Patient Administration interface, which may result in the need for rescans.
FDA Z-3277-2026
Medical Device High
Oct 7, 2026 Recall: Aug 11, 2026
Details
Embosphere 500-700 micrometer 2 mL Syringe Sterile Steam, REF: S420GH/EUA, S620GH/EUA; Embosphere 700-900 micrometer 2 mL Syringe Sterile Steam, REF: S820GH/CAB; Embosphere 900-1200 micrometer 2 mL Syringe Sterile Steam, REF: S1020GH/C, S1020GH/EUA
Microspheres used in embolization of tumors, prostatic arteries, arteriovenous malformations, and blood vessels may have holes in packaging that may affect the sterile barrier, which if used could lead to infection.
FDA Z-3305-2026
Medical Device High
Oct 7, 2026 Recall: Aug 10, 2026
Details
FDA Z-3327-2026
Medical Device High
Oct 7, 2026 Recall: Jul 17, 2026
Details
FDA Z-0037-2027
Medical Device High
Oct 7, 2026 Recall: Aug 24, 2026
Details
FDA Z-0022-2027
Medical Device High
Oct 7, 2026 Recall: Aug 24, 2026
Details
Ingenia 3.0T and 3.0T CX; Model number (REF): 1. 781342 (3.0T), 2. 781377 (3.0T), 3. 782103 (3.0T), 4. 781271 (3.0T CX); Software Versions: R11, R12 and R13;
When exporting diffusion tensor imaging (DTI) scans from a MR system using the Enhanced MR DICOM format, the exports contain incorrect data (diffusion directions). If the Enhanced MR DICOM export is used in conjunction with third-party software for tractography (e.g. for mapping nerve fiber pathways in the brain), the software will not be able to correctly process the DTI data for reconstruction.
FDA Z-3309-2026
Medical Device High
Oct 7, 2026 Recall: Aug 28, 2026
Details
Medline Basic Homecare Beds and Medlite Homecare Beds and Accessories MDR107000P BED, MANUAL, MEDLITE
Potential fire hazard involving the hand control pendant and associated wiring used with affected beds. Pendant or pendant wiring may overheat, potentially leading to smoking, sparking, melting, burning, or fire. Additional products added to 11/26/2025 recall.
FDA Z-3228-2026
Medical Device High
Oct 7, 2026 Recall: Aug 14, 2026
Details
FDA Z-0004-2027
Medical Device High
Oct 7, 2026 Recall: Aug 24, 2026
Details
Wire Harness and Busbar May Overheat
E-One Incorporated (E-One) is recalling certain 2024-2026 Typhoon N, 2025-2026 Cyclone N, and 2026 Cyclone II fire trucks. The positive power supply may be loose, causing the wiring harness and busbar to overheat. An overheated busbar can increase the risk of a fire.
NHTSA 26V652000
Vehicle Unknown
Oct 6, 2026 Recall: Oct 6, 2026
Details
FSIS Issues Public Health Alert for Ineligible Chicken Vienna-Style Sausage Products Illegally Imported From Jamaica
WASHINGTON, October 6, 2026 – The U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) is issuing a public health alert for canned chicken Vienna-style sausages that were illegally imported from Jamaica, a country that is not eligible to export meat or poultry products to the United States. FSIS is continuing to investigate how these products entered the country. The following products are subject to the public health alert, regardless of the product date [ view labels ]: 140-g. cans of “GRACE READY TO EAT CHICKEN VIENNA SAUSAGES.” 140-g. cans of “GRACE READY TO EAT CHICKEN VIENNA SAUSAGES HOT & SPICY.” The products bear establishment number “EST. NO G-01” inside the Jamaica mark of inspection. The importer subsequently distributed the product to retail locations in Alabama, Florida, Georgia, Maryland, and Texas. The problem was discovered during routine FSIS surveillance activities of imported products in commerce. There have been no confirmed reports of illness or injury due to consumption of these products. Anyone concerned about an illness or injury should contact a health care provider. FSIS is concerned that some product may be in consumers’ pantries. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase. Media and consumers with questions regarding the public health alert can contact Sandra Campbell, owner, at 305-887-9523 or [email protected] . Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to [email protected] . For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/ .
FSIS PHA-10062026-01
Food Medium
Oct 6, 2026 Recall: Oct 6, 2026
Details
Bus May Move with Wheelchair Lift Deployed
Greenpower Motor Company Inc. (Greenpower) is recalling certain 2021 Nano Beast school buses. A control module interlock software error may allow the bus to move while the wheelchair lift is deployed. The bus moving while the wheelchair lift is in use increases the risk of injury.
NHTSA 26V643000
Vehicle Medium
Oct 5, 2026 Recall: Oct 5, 2026
Details
Incorrect Tire Inflation on Federal Placard
Forest River, Inc. (Forest River) is recalling certain 2026-2027 Sunseeker, Solera, and Forester recreational vehicles. The Federal Placard may have incorrect tire inflation listed. A tire can be overinflated after referencing the incorrect information, increasing the risk of a crash.
NHTSA 26V646000
Vehicle High
Oct 5, 2026 Recall: Oct 5, 2026
Details
Exterior Outlet May Lack GFCI Protection
Forest River, Inc. (Forest River) is recalling certain 2027 Surveyor recreational trailers. The exterior receptacle may not be wired to a GFCI circuit. An outlet without GFCI protection may fail to shut off electrical power when a ground-fault occurs, increasing the risk of injury.
NHTSA 26V647000
Vehicle Medium
Oct 5, 2026 Recall: Oct 5, 2026
Details
Front Brake Hose May Leak
Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2022-2025 S 500 4MATIC, Maybach S 580 4MATIC, Maybach S 680 4MATIC, S 580 4MATIC, 2023-2025 S 580 E 4MATIC, and 2024-2025 AMG S 63 E Performance vehicles. The front brake hoses may rupture and leak brake fluid. A brake fluid leak can extend the distance needed to stop the vehicle, increasing the risk of a crash.
NHTSA 26V638000
Vehicle High
Oct 2, 2026 Recall: Oct 2, 2026
Details
Improperly Installed Seat Belt Component
Mercedes-Benz is recalling certain 2027 CLA 220 vehicles. A component of the left front seat belt may have been installed incorrectly. A seat belt with an incorrectly installed component may fail to properly restrain occupants, increasing the risk of injury during a crash.
NHTSA 26V636000
Vehicle High
Oct 2, 2026 Recall: Oct 2, 2026
Details
Platform Access Step May Separate from Vehicle
Altec Industries, Inc. (Altec) is recalling certain 2020-2026 AA Series Aerial Device, 2021-2026 AN Series Aerial Device, 2023-2026 AM Series Aerial Device, and 2024-2026 Digger Derrick, and 2024-2025 A-Class vehicles. The turntable mounted platform access step may have been improperly welded between the step tube and mounting plate, and allow the step to separate from the vehicle. A step that separates or becomes unstable while in use, increases the risk of a fall or injury.
NHTSA 26V637000
Vehicle Medium
Oct 2, 2026 Recall: Oct 2, 2026
Details
Rear Bumper Hitch Plate May Bend
Ring Power Corporation (Ring Power) is recalling certain 2020 Terex General 65, 2020-2021 C6000, 2020-2022 C4000, and TC55 vehicles. The incorrect pintle hitch may have been installed without reinforced bracing, resulting in the rear bumper hitch plate bending. The pintle hitch may fail, causing a loss of trailer control and increasing the risk of a crash.
NHTSA 26V639000
Vehicle High
Oct 2, 2026 Recall: Oct 2, 2026
Details
Do Not Drive: Cracked Weld May Cause Wheel and/or Tire Failure
Rosenbauer America (Rosenbauer) is recalling certain 2024-2025 Commander and 2024 Warrior fire engines. The rim weld may crack, causing the wheel to separate and tire to deflate. Wheel and/or tire failure increases the risk of a crash.
NHTSA 26V640000
Vehicle Critical
Oct 2, 2026 Recall: Oct 2, 2026
Details
High Voltage Battery Mounting Bolts May Be Loose or Missing
Blue Bird Body Company (Blue Bird) is recalling certain 2018-2024, 2026 Vision and All American Electric school buses. The high voltage battery system mounting bolts may be loose or missing. A high voltage battery with loose or missing mounting bolts can cause a loss of drive power, increasing the risk of a crash.
NHTSA 26V641000
Vehicle High
Oct 2, 2026 Recall: Oct 2, 2026
Details
Showing 601 - 625 of 4,975 product recalls

Product Recalls Today

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Latest Recalls By Source Agency

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CPSC

Latest Consumer Product Recalls

New alerts for toys, furniture, appliances, electronics, baby products, household goods and products with injury, choking, fire or fall hazards.

FDA

Latest Food And Medical Device Recalls

Recent FDA notices can include Class I, Class II and Class III recalls, market withdrawals, safety alerts, code information and distribution areas.

USDA FSIS

Latest Meat And Poultry Recall Alerts

FSIS alerts cover meat, poultry and egg products, including public health alerts, undeclared allergens, pathogen risks and misbranding issues.

NHTSA

Latest Vehicle Recall Campaigns

New vehicle, tire, equipment and child-seat campaigns include defect summaries, affected units, remedy notes and NHTSA campaign numbers.

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Check The Publish Date First

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Prioritize High-Risk Notices

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Verify The Official Notice

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Latest Product Recalls FAQ

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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.

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