The Recall Desk

State

California product recalls

73,100 recalls have nationwide distribution and so reach California. 13,251 additional recalls listed California specifically in their distribution scope.

What the numbers show

Total
13,251
Critical
1,605
Severe
2,846
Most recent
2026-09-25

Of the 13,251 recalls naming California we have scored against our rubric, 1,605 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,846 (21%) are Severe.

These figures cover only the 13,251 recalls whose distribution notice names California specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10901–10925 of 86351

  • HighNHTSA·24V679000·2024-09-12

    Maserati Recalls 2024 GranTurismo and GranCabrio for Software Defect

    Maserati is recalling 2024 GranTurismo and GranCabrio vehicles because body control module software may display incorrect fuel levels, potentially causing engine stalls.

    Product
    MASERATI — MASERATI GRANTURISMO, NUOVA GRANCABRIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24361·2024-09-12

    GOETAS Pool Drain Covers Recalled for Entrapment Hazard

    GOETAS pool drain covers do not meet Virginia Graeme Baker Pool and Spa Safety Act requirements and pose an entrapment hazard to swimmers. About 2,500 units sold on Amazon.com from March 2022 through July 2024 are affected.

    Product
    GOETAS Pool Drain Covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V678000·2024-09-12

    2024 Land Rover Discovery Sport rearview camera display malfunction

    The rearview camera image may not display on certain 2024 Land Rover vehicles due to a faulty Near Field Sensing Module that can overheat. Dealers will replace the module at no cost.

    Product
    LAND ROVER — LAND ROVER DEFENDER, RANGE ROVER VELAR, DISCOVERY SPORT, RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V680000·2024-09-12

    Kawasaki Recalls 2024 Z7 and Ninja 7 Hybrid Motorcycles for ECU Defect

    Kawasaki is recalling 2024 Z7 Hybrid and Ninja 7 Hybrid motorcycles because the electronic control unit may cause the transmission to shift into neutral, increasing crash risk.

    Product
    KAWASAKI — KAWASAKI NINJA 7 HYBRID, Z7 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24357·2024-09-12

    Stanley Jr. Kids Garden Sets Recalled for Excessive Lead in Paint

    Red Toolbox is recalling Stanley Jr. Kids Wheelbarrow and 7-piece Garden Sets sold at Costco because the painted long hoe and rake contain lead levels exceeding the federal ban, creating a poisoning hazard for children.

    Product
    Stanley Jr. Kids Wheelbarrow and 7-piece Garden Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V681000·2024-09-12

    Altec Aerial Lift and Pressure Digger Vehicles Recalled for Circuit Overload

    Altec is recalling 2023-2024 Aerial Device, Digger Derrick, and Pressure Digger vehicles due to an overloaded chassis ignition circuit that can cause engine shutdown and increase crash risk.

    Product
    ALTEC — ALTEC DIGGER DERRICK, PRESSURE DIGGER, AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V677000·2024-09-12

    Jaguar Recalls 2024 F-Pace Vehicles Due to Camera Display Failure

    Jaguar is recalling 2024 F-Pace vehicles because the Near Field Sensing Module may overheat, preventing the rearview camera from displaying and increasing crash risk.

    Product
    JAGUAR — JAGUAR F-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24360·2024-09-12

    Cadet Apex72 Electric Heaters Recalled Due to Fire Hazard

    Glen Dimplex Americas is recalling about 12,900 Cadet-branded Apex72 electric heaters because the fan can malfunction and fail to turn on, causing the unit to overheat and ignite internally. One heater fire has been reported with no injuries.

    Product
    Cadet-branded Apex72 Electric Heaters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2943-2024·2024-09-11

    Trilogy Evo Ventilator Software Update for Identified Safety Issues

    Philips Respironics is issuing a mandatory software update (Version 1.05.10.00) for the Trilogy Evo Universal Ventilator to address safety issues identified in earlier recalls. Affected units should implement the update.

    Product
    Trilogy Evo Universal Ventilator, Model No. DS2000X11B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V669000·2024-09-11

    Tiffin Allegro Bay motorhome subframe truss collapse fire risk recall

    Tiffin is recalling 2022–2025 Allegro Bay motorhomes due to subframe truss collapse that can pinch electrical wiring and cause electrical arcing, increasing fire risk.

    Product
    TIFFIN — TIFFIN ALLEGRO BAY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V671000·2024-09-11

    Storyteller Overland Recalls 2024 GXV Hilt for Spare Tire Mount Defect

    Storyteller Overland is recalling 2024 GXV Hilt vehicles because the spare tire mount may not be secured properly, allowing the tire to detach.

    Product
    STORYTELLER OVERLAND — STORYTELLER OVERLAND GXV HILT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0649-2024·2024-09-11

    FDA Recalls Heparin Sodium Injection for Endotoxin Contamination

    Baxter Healthcare Corporation is recalling 44,208 containers of Heparin Sodium in Sodium Chloride Injection nationwide after endotoxin testing revealed out-of-limit results. The contamination poses a risk of serious adverse reactions in patients receiving the intravenous medication.

    Product
    HEPARIN SODIUM IN SODIUM CHLORIDE — HEPARIN SODIUM IN SODIUM CHLORIDE (HEPARIN SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2942-2024·2024-09-11

    Trilogy Evo EV300 Ventilator Mandatory Software Update for Safety Issues

    Philips Respironics is issuing a mandatory software update (Version 1.05.10.00) for Trilogy Evo EV300 ventilators to resolve previously identified safety issues. Approximately 90,910 US units and 56,273 international units are affected.

    Product
    Trilogy Evo EV300 -- Model Number/ Model Description: BL2200X15B Trilogy Evo, O2, Benelux EV300; BR2200X18B Trilogy Evo, O2, Brazil EV300; CA2200X12B Trilogy Evo, O2, Canada EV300; DE2200X13B Trilogy Evo, O2, Germany EV300; DS2200X11B Trilogy Evo, O2, USA EV300…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2690-2024·2024-09-11

    Vivo 45 LS Ventilator Recall: Potential Formaldehyde Emission Risk

    Breas Medical is recalling the Vivo 45 LS ventilator due to potential elevated formaldehyde emissions into the patient breathing airpath under specific conditions.

    Product
    Vivo 45 LS, pressure and volume ventilator capable of delivering continuous or intermittent ventilatory support for patients who require invasive or non-invasive mechanical ventilation, Model/Catalog Number: 230000 (230016, 230216)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1781-2024·2024-09-11

    Popsicle Jolly Rancher Frozen Pops Recalled for Undeclared Milk Allergen

    Unilever North America is recalling Popsicle Jolly Rancher Frozen Confection Pops nationwide due to undeclared milk, which poses a risk to consumers with milk allergies.

    Product
    Popsicle Jolly Rancher Frozen Confection Pop Net Wt 2.71 FL OZ (80 ML). Green Apple Blue Raspberry and Grape flavored. GTIN/UPC 10077567003727 Case UPC 77567003720
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2944-2024·2024-09-11

    Philips Respironics Trilogy Evo Ventilator Software Update Addresses Safety Issues

    Philips Respironics is issuing a mandatory software update (Version 1.05.10.00) for Trilogy Evo ventilators worldwide to resolve identified safety issues. Users must apply the update and review the updated User Manual.

    Product
    Trilogy Evo; Model No./Model Description -- AU2110X15B Trilogy Evo, Australia BL2110X15B Trilogy Evo, Benelux BR2110X18B Trilogy Evo, Brazil CA2110X12B Trilogy Evo, Canada DE2100X13B Trilogy Evo O2, Germany DE2110X13B Trilogy Evo, Germany DS2100X11B Trilogy Evo, O2…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1779-2024·2024-09-11

    Ground Cinnamon Recalled Nationwide for Elevated Lead Levels

    MAMTAKIM Inc. is recalling ground cinnamon products distributed to nine states due to elevated lead content. The 15 g paper carton product carries code 10C035.

    Product
    Scortisoara macinata/ Ground cinnamon, 15 g, Paper cartons, 20 pieces per paper carton
    Category
    Food
    Distribution
    9 states
  • HighFDA (Food)·F-1774-2024·2024-09-11

    Reser's Creamy Deluxe Potatoes Recalled for Temperature Abuse Risk

    Reser's Fine Foods is recalling 182 cases of Potatoes Creamy Deluxe Special Request due to temperature abuse that may cause food spoilage.

    Product
    Item 71117.14446, Potatoes Creamy Deluxe Special Request, refrigerated product, net wt. 5lb. There are 4 packs per case.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Food)·F-1777-2024·2024-09-11

    Refrigerated Pasta Salad Recalled for Temperature Abuse and Spoilage Risk

    Reser's Fine Foods is recalling Stonemill Kitchens Green Goddess Pasta Salad due to potential spoilage from temperature abuse caused by a malfunctioning refrigeration unit. The product was distributed in CA, IL, MN, ND, and SD.

    Product
    Item 71117.18531, Stonemill Kitchens Green Goddess Pasta Salad, refrigerated product, net wt. 5lb. There are 2 packs per case.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-2947-2024·2024-09-11

    BD Pyxis QFill Medication Cabinet Software Issue Causes Incorrect Bin Labeling

    A software bug in BD Pyxis QFill medication cabinet systems may print incorrect medication bin labels during restocking, potentially causing medication errors. Three units are affected.

    Product
    BD Pyxis QFill Replenishment Station, REF: 138904-01, medication cabinet system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1546-2024·2024-09-11

    Beckman Coulter DxI 9000 Analyzer Recalled for Leaking Wash Buffer Tank

    Beckman Coulter is recalling 17 DxI 9000 Access Immunoassay Analyzers due to cracks in the Internal Wash Buffer Tank that can cause leaking, potentially delaying test results and exposing users to chemical and physical hazards.

    Product
    DxI 9000 Access Immunoassay Analyzer, REF C11137, vitro diagnostic device used for the quantitative, semi-quantitative, or qualitative determination of various analyte concentrations found in human body fluids.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0653-2024·2024-09-11

    Compounded Semaglutide Recalled Due to Lack of Sterility Assurance

    ProRx LLC is recalling 1,960 vials of compounded semaglutide nationwide due to lack of assurance of sterility. The multiple-dose vials may not meet sterility standards for injectable medications.

    Product
    SEMAGLUTIDE 10mg/4mL (2.5mg/mL), 4 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC 84139-225-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2952-2024·2024-09-11

    Desflurane anesthesia vaporizer recalled for possible excessive anesthetic output

    Mindray's Desflurane E_Vap vaporizer may deliver anesthetic at higher concentrations than set due to an incomplete seal. Patients could inhale excessive anesthetic, potentially causing dizziness, drowsiness, and in severe cases, neurological effects.

    Product
    Desflurane E_Vap.(Saf-T-Fill) used with the A9 Anesthesia System-Used to provide the vapor of an anesthetic agent with controllable concentration to an A9 anesthesia system. Part Number: Part Number115-066759-00
    Category
    Medical Device
    Distribution
    8 states