The Recall Desk

State

California product recalls

20,082 recalls have nationwide distribution and so reach California. 0 additional recalls listed California specifically in their distribution scope.

About recalls in California

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect California consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

5901–5925 of 20082

  • HighFDA (Devices)·Z-1194-2025·2025-02-26

    Medical device recall: RayStation radiation therapy software dose calculation inconsistency

    RayStation radiation therapy treatment planning software contains an inconsistency in density uncertainty calculations that may affect dose accuracy for proton and light ion treatments. The issue affects systems using HU-to-mass density CT calibration curves from RayStation versions 4.5 through 2024B.

    Product
    Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 5.0.2.35 and 5.0.3.17 Software Version: RayStation 5 Service Pack 2 and 3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0235-2025·2025-02-26

    Atomoxetine Capsules Recalled Due to Excess N-Nitroso Impurity

    Glenmark Pharmaceuticals is recalling Atomoxetine capsules due to the presence of N-Nitroso Atomoxetine impurity above FDA recommended limits. The nationwide recall affects 80,160 bottles.

    Product
    ATOMOXETINE — ATOMOXETINE (ATOMOXETINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1201-2025·2025-02-26

    remel Blood Agar EMB Agar Biplate Recalled for Listeria Contamination

    Remel's blood agar culture media plates (lot 213971) may contain Listeria monocytogenes contamination visible on the blood side. The affected product was distributed nationwide; users should discontinue use immediately.

    Product
    remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0227-2025·2025-02-26

    Lorazepam Tablets Recalled for Failed Impurity and Potency Specifications

    The FDA is recalling 94,349 cartons of Lorazepam 1mg tablets due to out-of-specification results for impurities and sub-potency discovered during routine stability testing. The affected product was distributed nationwide in the U.S. and Puerto Rico.

    Product
    LORAZEPAM — LORAZEPAM (LORAZEPAM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1176-2025·2025-02-26

    3M V.A.C. VIA Negative Pressure Wound Therapy System Recalled for Leak Alarm Malfunctions

    KCI USA is recalling approximately 2,169 units of the 3M V.A.C. VIA negative pressure wound therapy system due to increased complaints about leak alarm malfunctions affecting certain units.

    Product
    3M V.A.C. VIA Negative Pressure Wound Therapy System REF: VIAKIT077D01/US - V.A.C. VIA 7 Day Kit VIAKIT07S05/AU - V.A.C. VIA Starter Kit 65-Pack VIAKIT077D01/GB - V.A.C. VIA 7 Day Kit, Single Shipper
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1175-2025·2025-02-26

    3M Prevena Plus Negative Pressure Therapy System Recalled for Leak Alarm Malfunctions

    KCI USA is recalling 3M Prevena Plus wound therapy systems due to complaints about malfunctioning leak alarms. The recall affects 135,268 units distributed worldwide.

    Product
    3M Prevena Plus 125 Therapy Unit and System Kits REF: PRE3021US Prevena Plus Duo Peel and Place 20cm System Kit, US PRE3201US Prevena Plus Peel and Place 35 cm system Kit, US PRE3201 Prevena Plus Peel and Place 35 cm system Kit PRE4000US Prevena Plus 125 Therapy Unit, U
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0234-2025·2025-02-26

    Atomoxetine capsules recalled due to elevated N-nitroso impurity

    Glenmark Pharmaceuticals is recalling Atomoxetine 40 mg capsules nationwide due to manufacturing deviations. Some lots contain N-nitroso Atomoxetine impurity above FDA-recommended limits.

    Product
    ATOMOXETINE — ATOMOXETINE (ATOMOXETINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1202-2025·2025-02-26

    Dexcom G6 Glucose Monitor May Fail to Deliver Alarms Properly

    Dexcom G6 continuous glucose monitors may fail to deliver high or low blood sugar alarms due to a software error, potentially delaying detection of dangerous glucose levels. Alarms will be delayed and skip in sequence until the device is reset.

    Product
    Dexcom G6, Continuous Glucose Monitoring System, REFs: STK-OM-001, STR-OM-001, STR-OR-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0243-2025·2025-02-26

    Atomoxetine Capsules Recalled Due to N-Nitroso Impurity Contamination

    Glenmark Pharmaceuticals is recalling approximately 58,416 bottles of Atomoxetine 80 mg capsules nationwide due to the presence of N-Nitroso Atomoxetine impurity above FDA-recommended limits. This is a Class II recall.

    Product
    ATOMOXETINE — ATOMOXETINE (ATOMOXETINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1189-2025·2025-02-26

    Radiation Therapy Planning System Density Calculation Inconsistency in RayStation

    RayStation radiation therapy planning software versions 4.5 through 2024B contain an inconsistency in how density uncertainty is handled in dose calculation functions for proton and light ion therapy plans.

    Product
    Brand Name: RayStation- Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 1.0.0.951, 11.0.1.29, 11.0.3.116 and 11.0.4.15 Software Revisions: RayStation 11A and 11A Service Pack 1, 2 and 3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1186-2025·2025-02-26

    RayStation radiation therapy planning software density uncertainty calculation inconsistency

    RayStation radiation therapy planning software versions 4.5 through 2024B contain an inconsistency in density uncertainty handling when HU-to-mass density CT calibration curves are used. No illnesses or injuries have been reported.

    Product
    Brand Name: RayStation -Intended as a Radiation Therapy Treatment Planning System Model/Catalog Number: 8.1.0.47, 8.1.1.8, 8.1.2.5, 9.0.0.113 and 9.0.1.142 Software Version: RayStation 8B, 8B Service Pack 1 and 2, 9A and 9A Service Pack 1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1199-2025·2025-02-26

    Patient Warming Mattress Recalled for Cable Connection Defect

    Augustine Temperature Management recalls 3 Hot Dog patient warming mattresses (US530) due to cable connector deflection that may cause intermittent connection failure, potentially occurring after one year of use.

    Product
    Hot Dog PATIENT WARMING, Underbody Warming Mattress + Return Electrode, 89 cm (35"), REF US530, to prevent or treat hypothermia
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1181-2025·2025-02-26

    AnchorFast Guard Endotracheal Tube Fasteners Recalled Due to Tube Migration Risk

    Hollister is recalling AnchorFast Guard endotracheal tube fasteners because decreased skin barrier wear time could cause tube migration. The recall affects multiple lot numbers distributed in the US and Canada.

    Product
    AnchorFast Guard, Oral Endotracheal Tube Fastener, REF 9800,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0238-2025·2025-02-26

    Atomoxetine Capsules Recalled for Chemical Impurity Above FDA Limits

    Glenmark Pharmaceuticals is recalling 120,000 bottles of Atomoxetine 10 mg capsules nationwide due to N-nitroso Atomoxetine impurity exceeding FDA recommended limits. Multiple lot numbers are affected with expiration dates through July 2026.

    Product
    ATOMOXETINE — ATOMOXETINE (ATOMOXETINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·25150·2025-02-20

    SuperATV Carrier Bearings for Polaris RZR Recalled for Fire and Burn Hazards

    SuperATV carrier bearings for Polaris RZR XP Turbo or Turbo S vehicles can allow the drive shaft to contact the fuel tank, causing fuel leaks and fire hazards. SuperATV is offering free replacement bearings to affected consumers.

    Product
    SuperATV carrier bearings for Polaris RZR XP Turbo or Turbo S Recreational Off Highway Vehicles (ROVs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25137·2025-02-20

    Electra E-Bikes Recalled Due to Crash Hazard From Loose Rear Fender

    Trek is recalling about 927 Electra e-bikes because the rear fender can come loose, contact the rear wheel, and stop the bike unexpectedly, posing a crash hazard. One injury with a fractured shinbone and meniscus tear has been reported.

    Product
    Electra E-bikes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25138·2025-02-20

    Swagtron SG-5 Boost Electric Scooters Recalled for Fire and Burn Hazards

    Walmart recalls about 17,970 Swagtron SG-5 Boost electric scooters due to lithium-ion batteries that can overheat, smoke, and ignite, causing fire and burn hazards. One incident caused a burn injury and property damage to a residential building.

    Product
    Swagtron SG-5 Swagger 5 Boost Commuter Electric Scooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25140·2025-02-20

    DR Power Equipment Tow Behind Mowers Recalled for Detaching Blade Risk

    DR Power is recalling about 890 tow behind field and brush mowers because the blade carrier spindle bolt can loosen, causing the blade assembly to detach and pose a laceration hazard. No injuries reported.

    Product
    Tow Behind Field and Brush Mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25144·2025-02-20

    Triumph TF250-X Motorcycles Recalled for Electrical Short Circuits and Unintended Starting

    About 690 Triumph TF250-X motorcycles are recalled due to plastic switch cubes that crack when exposed to brake fluid, creating electrical short circuits that can cause the motorcycle to start unexpectedly. No injuries have been reported.

    Product
    Triumph TF250-X Closed Course Competition Motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25149·2025-02-20

    Super73 Electric Bicycles Recalled for Brake Failure and Crash Hazard

    Super73 is recalling about 1,400 Model Year 2024 Z Miami SE and Z Adventure Core e-bikes sold April-September 2024. A retaining pin in the disc brake calipers can dislodge, causing brake failure and crash/injury hazards.

    Product
    Model Year 2024 Z Miami SE and Z Adventure Core Electric Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25145·2025-02-20

    SEJOV Five-Drawer Dressers Recalled for Tip-Over and Entrapment Hazards

    About 900 SEJOV five-drawer dressers sold on Amazon from September 2023 through August 2024 are unstable if not properly anchored to a wall, posing tip-over and entrapment hazards to children. No injuries have been reported.

    Product
    SEJOV Five-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25142·2025-02-20

    Fjorden iPhone Camera Grips Recalled for Coin Battery Ingestion Hazard

    Fjorden iPhone Camera Grips can release their coin batteries if dropped, creating an ingestion hazard for children. Swallowed coin batteries can cause serious internal injuries, chemical burns, and death.

    Product
    Fjorden iPhone Camera Grips
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25143·2025-02-20

    Holosun firearm dot sights recalled for lithium battery ingestion hazard

    Holosun has recalled approximately 9,400 firearm dot sights with accessible lithium coin batteries that pose an ingestion hazard. The products violate federal safety regulations by lacking child-resistant packaging and required warning labels.

    Product
    Holosun Firearm Dot Sights
    Category
    Consumer Product
    Distribution
    Distributed nationwide