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 |
|---|---|---|---|---|---|
|
FDA
Z-3328-2026
|
Medical Device | High |
Oct 7, 2026
Recall: Jul 17, 2026
|
Details | |
|
Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT, GYN LAPAROSCOPY NEW HAN , Catalog Number: PB23GLNLAC; 2) KIT, GYN LAPAROSCOPY NEW HAN , Catalog Number: PB23GLNLA1; 3) KIT, GYN LAPAROSCOPY NEW HAN , Catalog Number: PB23GLNLA2; 4) KIT, GYN LAPAROSCOPY NEW HAN , Catalog Number: PB23GLNLA3; 5) KIT, GYN LAPAROSCOPY NEW HAN , Catalog Number: PB23GLNLA4; 6) KIT, GYN ROBOTIC NEW HAN , Catalog Number: PB23GRNLD; 7) KIT, GYN ROBOTIC NEW HAN , Catalog Number: PB23GRNLE; 8) KIT, GYN ROBOTIC NEW HAN , Catalog Number: PB23GRNL5; 9) KIT, GYN ROBOTIC NEW HAN , Catalog Number: PB23
The kits contain tube sets with handpieces that may leak during use. The impacted devices can have the following failures: fluid leakage from the hand piece that can pool on the floor. The impact can range from user dissatisfaction to the potential for the user of slip and fall.
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FDA
Z-3297-2026
|
Medical Device | High |
Oct 7, 2026
Recall: Aug 18, 2026
|
Details |
|
Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 20" X 6" 1-LINE (CS 10) NAVY BLUE Model/Catalog Number: 564017 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No
Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
|
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 |
|
Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 44" 2 LINE (10) Model/Catalog Number: DT-7044-02Q Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No
Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
|
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 | |
|
Brand Name: Expressaire Product Name:DISPOSABLE BB TOURNQUET CUFF, 26" X 6" DUAL BLADDER, 2-LINE (CS 12) ORANGE Model/Catalog Number: A70107017 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No
Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
|
FDA
Z-0037-2027
|
Medical Device | High |
Oct 7, 2026
Recall: Aug 24, 2026
|
Details |
|
Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 8" X 2.5" 2-LINE (CS 12) LIGHT BLUE Model/Catalog Number: A70107001 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No
Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
|
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 |
|
Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 30" X 4" 2-LINE (CS 18) WHITE Model/Catalog Number: 553323 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to reduce or totally occlude circulation during surgery. It is non-invasive device. Tourniquet Cuffs are intended for use in surgical procedures that requires the interruption of blood flow and clear visualization of the operative field. Component: No
Due to incorrect expiration date on product manufactured between September 2016 to March 2023. Products are labeled with a 10 year shelf life. The correct validated shelf life is 5 years.
|
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 |
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.
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