The Recall Desk

Archive

October 2026 recalls

661 recalls were announced in October 2026.

What the numbers show

Critical
10
Severe
205
High
122
Moderate
309
Low
15

Of the 661 recalls this month scored against our rubric, 2% are Critical, 31% are Severe.

601–661 of 661

  • ModerateFDA (Devices)·Z-3283-2026·2026-10-07

    United Imaging uMI 550 PET/CT Systems Recalled for Software Defect

    FDA is recalling 34 United Imaging uMI 550 PET/CT systems due to a software issue that can hide patient images, potentially requiring rescans.

    Product
    Positron Emission Tomography and Computed Tomography System, Model: uMI 550 with software
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0052-2027·2026-10-07

    FDA Recalls MPR Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.

    Product
    Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 18" 1 LINE (10) Model/Catalog Number: DT-7018-01Q 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…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3318-2026·2026-10-07

    Philips MRI Systems Recalled for Incorrect Diffusion Tensor Imaging Data Exports

    Philips is recalling 91 Evolution MRI systems because Enhanced MR DICOM exports contain incorrect diffusion directions, preventing correct tractography reconstruction.

    Product
    Evolution upgrade 1.5T amd Evolution upgrade 3.0T; Model number (REF): 1. 782116 (1.5T), 2. 782148 (1.5T), 3. 782166 (1.5T), 4. 782201(1.5T), 5. 782117 (3.0T), 6. 782143 (3.0T), 7. 782162 (3.0T); Software Versions: R11, R12 and R13;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3309-2026·2026-10-07

    Philips Ingenia MRI Systems Recalled for Incorrect DTI Data Exports

    Philips is recalling Ingenia 3.0T MRI systems because diffusion tensor imaging exports contain incorrect data, preventing accurate tractography reconstruction.

    Product
    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;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0013-2027·2026-10-07

    ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.

    Product
    Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 30" X 4" 2-LINE (CS 10) WHITE Model/Catalog Number: 564011 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0046-2027·2026-10-07

    ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global is recalling sterile disposable tourniquet cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.

    Product
    Brand Name: ASP Global Product Name:DISPOSABLE TOURNIQUET CUFF, 34" X 4" 2-Line, Blue Model/Catalog Number: ASP-564013 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0058-2027·2026-10-07

    Recall of MPR Single Use Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.

    Product
    Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 34" 2 LINE (10) Model/Catalog Number: DT-7034-02Q 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…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3313-2026·2026-10-07

    Philips MR 7700 MRI Systems Recalled for Incorrect DTI Data Exports

    Philips is recalling 107 MR 7700 MRI systems because diffusion tensor imaging (DTI) exports contain incorrect data, preventing accurate tractography reconstruction.

    Product
    MR 7700; Model number (REF): 1. 782120, 2. 782153, 3. 782155, 4. 782199; Software Versions: R11, R12 and R13;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0056-2027·2026-10-07

    MPR Single Use Tourniquet Cuff Recalled for Incorrect Expiration Date

    ASP Global, LLC. is recalling MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.

    Product
    Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 30" 2 LINE (10) Model/Catalog Number: DT-7030-02Q 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…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3326-2026·2026-10-07

    Micro Therapeutics Recalls Pipeline Flex Embolization Device Due to Labeling Error

    Micro Therapeutics is recalling two units of the Pipeline Flex Embolization Device with Shield Technology because the packaging label incorrectly listed the diameter as 3.00 mm when the actual unit was 2.50 mm.

    Product
    Pipeline Flex Embolization Device with Shield Technology REF PED2-300-12 UDI-DI code: 00763000448806 he Pipeline Flex Embolization Device with Shield Technology consists of a permanent implant combined with a guidewire based delivery system. The Pipeline Flex Embolization…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0004-2027·2026-10-07

    ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.

    Product
    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…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0063-2027·2026-10-07

    Recall of MPR Single Use Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global is recalling 80 MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life, but the validated shelf life is 5 years.

    Product
    Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 12" 2 LINE (10) Model/Catalog Number: DT-7112-02Q 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…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0065-2027·2026-10-07

    ASP Global Recalls MPR Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global, LLC. is recalling 180 units of MPR Single Use Tourniquet Cuffs because they are labeled with a 10-year shelf life instead of the correct 5-year validated shelf life.

    Product
    Brand Name: MPR Product Name:SINGLE USE TOURNIQUET CUFF 15" 2 LINE (10) Model/Catalog Number: DT-7115-02Q 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…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0029-2027·2026-10-07

    ASP Global Recalls Disposable Tourniquet Cuffs Due to Incorrect Expiration Dates

    ASP Global, LLC. is recalling Expressaire Disposable Tourniquet Cuffs because the products are labeled with a 10-year shelf life, but the correct validated shelf life is 5 years.

    Product
    Brand Name: Expressaire Product Name:DISPOSABLE TOURNIQUET CUFF, 24" X 4" 1-LINE (CS 18) YELLOW Model/Catalog Number: A70107008 Software Version: Not Applicable Product Description: Sterile Disposable Tourniquet Cuff is used to be wrapped around a patient's limb and inflated…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-3317-2026·2026-10-07

    Philips MR 7700 Software Upgrade Recalled for Incorrect DTI Data

    Philips is recalling 30 MR 7700 software upgrades because they export incorrect diffusion tensor imaging data, preventing accurate nerve fiber mapping.

    Product
    Upgrade to MR 7700; Model number (REF): 782130; Software Versions: R11, R12 and R13;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-3270-2026·2026-10-07

    HeartSine Defibrillators Recalled for Missing Maintenance Supplement

    HeartSine Technologies is recalling 31,834 public access defibrillators distributed without the required Maintenance Supplement, which describes an extra check every 3 months.

    Product
    HeartSine samaritan PAD (Public Access Defibrillator); HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English (American Airlines) - 2 Min CPR UDI-DI code: 0506016712207 350P US Device, US English with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-3333-2026·2026-10-07

    Karl Storz Recalls HOPKINS Telescope Eyepieces Due to Labeling Error

    Karl Storz Endoscopy is recalling six HOPKINS Telescope eyepieces because of incorrect inside packaging labels. The units were distributed in Arizona, California, and Missouri.

    Product
    HOPKINS Telescope 30¿, 4mm REF 10005BA UDI-DI code: 04048551045121 KARL STORZ HOPKINS¿ and HOPKINS¿ II telescopes are to be used for visualization of the surgical site during diagnostic and therapeutic endoscopic procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V656000·2026-10-06

    Great Dane Recalls 2027 Champion Trailers Due to Coupler Defect

    Great Dane is recalling 2027 Champion dry van trailers because an incorrect coupler plate may prevent proper coupling, increasing crash risk.

    Product
    GREAT DANE — GREAT DANE CHAMPION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V655000·2026-10-06

    Ford Recalls 2025-2027 F-150 Trucks Due to Improperly Secured Front Seats

    Ford is recalling 2025-2027 F-150 vehicles because front seats may be improperly secured, increasing injury risk in a crash. Dealers will inspect and repair the seats free of charge.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V652000·2026-10-06

    E-One Recalls Fire Trucks Due to Wiring Overheat Risk

    E-One is recalling specific Typhoon N, Cyclone N, and Cyclone II fire trucks because a loose power supply may cause wiring to overheat, increasing fire risk.

    Product
    E-ONE — E-ONE TYPHOON N, CYCLONE N, CYCLONE II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V657000·2026-10-06

    KME Recalls 2024 CV515 SFA 4x4 and Severe Service Emergency Vehicles

    KME is recalling 2024 CV515 SFA 4x4 and Severe Service emergency vehicles because a node may become unresponsive, causing loss of exterior lighting and pump-mode functionality.

    Product
    KME — KME CV515 SFA 4X4, SEVERE SERVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V654000·2026-10-06

    Spartan Fire Recalls One 2024 Metrostar Emergency Vehicle for Node Defect

    Spartan Fire is recalling one 2024 Metrostar emergency vehicle because a node may become unresponsive, causing loss of exterior lighting or pump-mode functionality.

    Product
    SPARTAN FIRE — SPARTAN FIRE METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-10062026-01·2026-10-06

    USDA Issues Public Health Alert for Illegally Imported Chicken Sausage

    USDA FSIS issued a public health alert for canned chicken sausages illegally imported from Jamaica. Consumers in five states should discard the products.

    Product
    FSIS Issues Public Health Alert for Ineligible Chicken Vienna-Style Sausage Products Illegally Imported From Jamaica
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·26V648000·2026-10-05

    Kalmar Recalls Ottawa T2 Terminal Tractors Due to Fire Risk

    Kalmar is recalling 2014-2026 Ottawa T2 terminal tractors because damaged circuit board insulation may cause a short circuit and fire. Owners should park vehicles outside until repaired.

    Product
    KALMAR — KALMAR OTTAWA T2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V644000·2026-10-05

    New Flyer Recalls Buses Due to Hazard Light Indicator Defect

    New Flyer is recalling certain 2013-2027 buses because the instrument panel indicator light may not illuminate when hazard warning lights are active.

    Product
    NEW FLYER — NEW FLYER XE40, XDE60, XDE40, XD40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V646000·2026-10-05

    Forest River Recalls 2026-2027 RVs Due to Incorrect Tire Inflation Labels

    Forest River is recalling 2026-2027 Sunseeker, Solera, and Forester RVs because Federal Placards may list incorrect tire inflation, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER FORESTER, SOLERA, SUNSEEKER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V649000·2026-10-05

    REV Ambulance Group Recalls 2025-2027 Road Rescue and Wheeled Coach Ambulances

    REV Ambulance Group is recalling 2025-2027 Road Rescue and Wheeled Coach ambulances because a node may become unresponsive, causing a loss of warning lights and increasing crash risk.

    Product
    ROAD RESCUE — ROAD RESCUE, WHEELED COACH TYPE III, TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V645000·2026-10-05

    MCI Recalls 2018-2026 Buses for Hazard Light Indicator Defect

    MCI is recalling 2018-2026 buses because the instrument panel indicator light may not illuminate when hazard warning lights are active and the master run switch is off.

    Product
    MCI — MCI D45CRTLE, D45CRT, D4520, D4020ISTV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V643000·2026-10-05

    Greenpower Recalls 2021 Nano Beast School Buses Due to Software Error

    Greenpower is recalling 2021 Nano Beast school buses because a software error may allow the vehicle to move while the wheelchair lift is deployed.

    Product
    GREENPOWER — GREENPOWER NANO BEAST SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V642000·2026-10-02

    Blue Bird Recalls 2022-2024 All American Electric Transit Buses

    Blue Bird is recalling 2022-2024 All American Electric transit buses because high voltage battery mounting bolts may be loose or missing, increasing crash risk.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN TRANSIT BUS (ELECTRIC)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V638000·2026-10-02

    Mercedes-Benz Recalls S-Class Vehicles Due to Front Brake Hose Rupture Risk

    Mercedes-Benz is recalling certain 2022-2025 S-Class and Maybach vehicles because front brake hoses may rupture and leak fluid, increasing the risk of a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH S 580 E 4MATIC, S 580 4MATIC, S 680 4MATIC, AMG S 63 E 4MATIC+
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V640000·2026-10-02

    Rosenbauer Recalls 2024-2025 Fire Engines Due to Wheel Separation Risk

    Rosenbauer America is recalling 2024-2025 Commander and 2024 Warrior fire engines because rim welds may crack, causing wheel separation and tire deflation.

    Product
    ROSENBAUER — ROSENBAUER WARRIOR, COMMANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·025-2026·2026-10-02

    Inexport Logistics Recalls Ineligible Imported Pork Crackling Chips

    Inexport Logistics LLC is recalling approximately 189 pounds of potato chips containing pork cracklings imported from Colombia, a country ineligible to export meat to the US.

    Product
    Inexport Logistics LLC Recalls Ineligible Pork Cracklings Products Imported From The Republic of Colombia
    Category
    Food
    Distribution
    8 states
  • SevereNHTSA·26V641000·2026-10-02

    Blue Bird Recalls Electric School Buses Due to Loose Battery Bolts

    Blue Bird is recalling 2018-2026 electric school buses because high-voltage battery mounting bolts may be loose or missing, which can cause a loss of drive power.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN SCHOOL BUS (ELECTRIC), VISION SCHOOL BUS (ELECTRIC)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V639000·2026-10-02

    Ring Power Recalls Terex Vehicles Due to Potential Pintle Hitch Failure

    Ring Power is recalling certain Terex vehicles because an incorrect pintle hitch may have been installed without reinforced bracing, increasing the risk of a crash.

    Product
    TEREX — TEREX GENERAL 65, C6000, C4000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V637000·2026-10-02

    Altec Recalls Aerial Devices and Digger Derricks Due to Step Welding Defect

    Altec is recalling specific aerial devices and derrick vehicles because improperly welded platform access steps may separate, increasing the risk of falls or injuries.

    Product
    ALTEC — ALTEC AA SERIES AERIAL DEVICE, DIGGER DERRICK, A-CLASS, AN SERIES AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V636000·2026-10-02

    Mercedes-Benz Recalls 2027 CLA 220 Vehicles for Seat Belt Defect

    Mercedes-Benz is recalling 2027 CLA 220 vehicles because a left front seat belt component may be installed incorrectly, increasing crash injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ CLA 220
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V635000·2026-10-01

    Freightliner Recalls Business Class M2 Trucks for Fire Risk

    Daimler Trucks North America is recalling 2025-2027 Freightliner Business Class M2 vehicles because underbody insulation may contact hot exhaust components, increasing fire risk.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·27013·2026-10-01

    Golden Resale Recalls Portable Camping Showers Due to Fire Hazard

    Golden Resale is recalling portable camping showers with immersion heaters because they can ignite when out of water, posing a risk of serious injury or death.

    Product
    Portable Camping Showers with bucket and immersion heater
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·27014·2026-10-01

    Agrish Adult Portable Bed Rails Recalled for Entrapment and Fall Hazards

    Agrish is recalling adult portable bed rails due to risks of entrapment, asphyxiation, and falls. Consumers should stop using the products and contact the company for a refund.

    Product
    Agrish Adult Portable Bed Rails, models 12014, AG-12011 and 12016
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·27008·2026-10-01

    GBYMIUY Recalls Magnetic Stick Figure Toys Due to Ingestion Hazard

    GBYMIUY is recalling magnetic stick figure toy sets because loose high-powered magnets pose a risk of serious injury or death if swallowed by children.

    Product
    GBYMIUY Magnetic Stick Figure Toy Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·27003·2026-10-01

    ABC Trading Recalls Squishy Toys Due to Water Bead Ingestion Risk

    ABC Trading is recalling squishy dumpling and crazy squib ball toys because the water beads inside can expand and pose a deadly ingestion hazard to children.

    Product
    Squishy Dumpling Toys, Crazy Squib Ball Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E068000·2026-10-01

    Kuat Pivot V3 Swing-Away Hitch Adapter Recall for Weld Cracking

    Kuat Innovations is recalling Pivot V3 swing-away hitch adapters because a weld may crack, causing the cross beam to detach and create a road hazard.

    Product
    EQUIPMENT:MECHANICAL:CARRIER/RACK recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·27007·2026-10-01

    Designs Direct Recalls Three-Light Floor Lamps Due to Fire and Burn Hazards

    Designs Direct is recalling Cupcakes and Cashmere brand floor lamps because the cord or wiring can overheat, posing fire and burn risks. Consumers should stop using the lamps and request a refund.

    Product
    Designs Direct Cupcakes and Cashmere Brand Three-Light Floor Lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V632000·2026-10-01

    2027 Thomas Built Buses Recall for Headlight Software Error

    Daimler Trucks North America is recalling 2027 Thomas Built SAF-T-LINER C2 and Jouley school buses because a software error may cause low beam headlights to illuminate improperly.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2, SAF-T-LINER C2 JOULEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·27009·2026-10-01

    Gobi Heat Recalls Rechargeable Hand Warmers Due to Fire and Burn Hazards

    Gobi Heat is recalling rechargeable hand warmers because the lithium-ion batteries can overheat and ignite, posing a risk of serious injury from fire and burns.

    Product
    Gobi Heat Rechargeable Hand Warmers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·27012·2026-10-01

    Dollar Tree Recalls Electric Balloon Pumps Due to Burn Hazard

    Dollar Tree is recalling electric balloon pumps that can overheat, posing a burn hazard. Consumers should stop using the pumps and return them for a refund.

    Product
    Electric Balloon Pumps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·27010·2026-10-01

    Walmart Recalls Over 4.4 Million Metal Wire Bristle Grill Brushes

    Walmart is recalling over 4.4 million Expert Grill metal wire bristle grill brushes because detached bristles can stick to food, posing an ingestion hazard.

    Product
    Metal Wire Bristle Grill Brushes
    Category
    Consumer Product
    Distribution
    Distributed nationwide

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