The Recall Desk

State

California product recalls

73,219 recalls have nationwide distribution and so reach California. 13,255 additional recalls listed California specifically in their distribution scope.

What the numbers show

Total
13,255
Critical
1,605
Severe
2,847
Most recent
2026-10-02

Of the 13,255 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 2,847 (21%) are Severe.

Which agencies issued them

These figures cover only the 13,255 recalls whose distribution notice names California specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15876–15900 of 86474

  • HighFDA (Devices)·Z-0127-2024·2023-11-01

    TruDi Navigation System position discrepancy during ENT surgery

    A surgical navigation system used in ENT procedures may display incorrect curette tip positions, potentially causing delayed surgery, cerebrospinal fluid leaks, vision loss, or skull damage. The recall affects 141 units across 30 US states.

    Product
    TruDi Navigation System, Model: FG-2000-00, Catalog: ENS022B, when used with TruDi Curette, Models: TDC0005Z and TDC0005
    Category
    Medical Device
    Distribution
    30 states
  • HighFDA (Devices)·Z-0060-2024·2023-11-01

    Diagnostic Test Strips Recalled for Manufacturing Conformance and Documentation Issues

    Universal Meditech Inc. is recalling diagnostic test strips due to Quality System violations and lack of manufacturing documentation. The company is closing and cannot provide post-market surveillance or support.

    Product
    DiagnosUS¿ One Step FSH Menopausal Test (Strip) REF 210-07
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Food)·F-0301-2024·2023-11-01

    Dark Chocolate Peanut Butter Recalled for Undeclared Sesame Allergen

    Betty Lou's Inc. recalls Stabilyze Sugar Stable Dark Chocolate Peanut Butter due to undeclared sesame. The product was distributed across 26 states; consumers with sesame allergies should not consume it.

    Product
    Stabilyze Sugar Stable Dark Chocolate Peanut Butter, 50g (1.76 oz), sold individual package or box. Each package has UPC 0 16073 00213 1. There are 12 packages per display box (box UPC 0 16073 00223 0). The label allergens contains statement declares Milk, Peanut, Tree Nuts…
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-0155-2024·2023-11-01

    SOZO Bilateral Arm L-Dex Software inadequate lymphedema detection sensitivity

    Impedimed's SOZO Bilateral Arm L-Dex Software (versions 4.1 and 5.0) has inadequate sensitivity for detecting early lymphedema, which could delay treatment. The FDA is recalling 354 units distributed nationwide.

    Product
    SOZO Bilateral Arm L-Dex Software
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0049-2024·2023-11-01

    Pregnancy Test Recalled for Unverified Manufacturing Compliance and Firm Closure

    Universal Meditech Inc. is recalling the Am I Pregnant? One Step HCG Pregnancy Test because the company is going out of business and cannot verify manufacturing compliance or provide quality system documentation.

    Product
    Am I Pregnant? One Step HCG Pregnancy Test REF 100-17
    Category
    Medical Device
    Distribution
    8 states
  • HighFDA (Devices)·Z-0180-2024·2023-11-01

    Sub Q Recorder Pack components may lose functionality due to improper sterilization

    American Contract Systems is recalling Sub Q Recorder Pack components that were improperly sterilized using ethylene oxide at excessive temperatures. The I.V. Cath and Dermabond components may lose functionality or drug efficacy as a result.

    Product
    Sub Q Recorder Pack, REF BPRC87A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23E085000·2023-11-01

    Hollywood Racks Recalls 2022-2023 Destination E Rack Bicycle Carriers

    Hollywood Racks is recalling 2022-2023 Destination E Rack Bicycle Carriers because a component may fail, allowing a bike to detach and become a road hazard.

    Product
    EQUIPMENT:MECHANICAL:CARRIER/RACK recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0050-2024·2023-11-01

    Pregnancy test strips recalled due to manufacturing documentation gaps

    Universal Meditech Inc. is recalling To Life hCG pregnancy test strips because the company is ceasing operations and cannot verify manufacturing compliance. The firm cannot provide documentation of manufacturing standards, storage conditions, or post-market safety monitoring.

    Product
    To Life hCG Pregnancy Urine Test Strips Format REF Cat No: 100-10
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Devices)·Z-0053-2024·2023-11-01

    Multiple Diagnostic Test Strips Recalled for Unverified Quality Standards

    Universal Meditech Inc. is recalling multiple diagnostic test strips (breastmilk alcohol, SARS-CoV-2 antibody, and ketone tests) distributed in the U.S. and Taiwan because the company is closing and cannot provide documentation of manufacturing compliance or post-market surveillance records.

    Product
    PrestiBio Ovulation and Pregnancy Strips REF 100-4 and REF 200-4 60 LH Test Strips/+30 HCF Test Strips
    Category
    Medical Device
    Distribution
    8 states
  • ModerateFDA (Drugs)·D-0070-2024·2023-11-01

    Oxytocin IV Bags Recalled Due to Labeling Defect

    Denver Solutions recalls 6,276 IV bags of oxytocin due to a labeling defect. The product was distributed nationwide to healthcare facilities.

    Product
    Oxytocin synthetic, 30 Units added to 0.9% Sodium Chloride 500mL IV Bag (0.06 Units per mL), Rx only, Leiter Compounding Health, 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-157-70
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0159-2024·2023-11-01

    Embrace2 Seizure Monitor Recalled for Reduced Battery Life

    Empatica has recalled 1,360 units of its Embrace2 seizure monitoring wearable due to potential battery life lasting less than the specified 48 hours, requiring more frequent charging.

    Product
    Embrace2- Indicated for use as an adjunct to seizure monitoring of adults and children age 6 and up in home or healthcare facilities during periods of rest. Models: (1) Flamingo Pink EM2-FP-S; (2) Sky Blue EM2-SB-2; (3) Seoul Grey EM2-SG-S; (4) Boston Blue…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0071-2024·2023-11-01

    Vancomycin HCI IV bags recalled for labeling issue

    Denver Solutions is recalling 33,480 Vancomycin HCI IV bags (NDC 71449-028-68) due to a labeling issue. The affected lots were distributed nationwide.

    Product
    VANCOmycin HCI PF, 1.25 g added to 0.9% Sodium Chloride 250 mL IV Bag, Rx only, Leiters Compounding Health, 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-028-68.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0063-2024·2023-11-01

    Pregnancy test strips recalled for lack of FDA authorization and quality documentation

    Universal Meditech Inc. recalled DiagnosUS hCG pregnancy test strips because the company distributed them without FDA marketing authorization and cannot provide manufacturing compliance documentation. The firm is ceasing operations.

    Product
    DiagnosUS hCG Pregnancy Urine Test Strip Format REF 100-12
    Category
    Medical Device
    Distribution
    8 states
  • LowFDA (Drugs)·D-0072-2024·2023-11-01

    Vancomycin Hydrochloride IV Bags Recalled Nationwide for Labeling Issue

    Denver Solutions, LLC is recalling 25,908 Vancomycin HCI IV bags distributed nationwide due to a labeling issue. Affected lots include products with expiration dates from October 2023 through January 2024.

    Product
    VANCOmycin HCI PF, 1.5 g added to 0.9% Sodium Chloride 250 mL IV Bag, Rx only, Leiters Compounding Health, 13796 Compark Blvd, Englewood, CO 80112, NDC 71449-029-68.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V730000·2023-10-31

    Triumph Rocket 3 rear brake master cylinders may extend stopping distance

    Triumph is recalling certain 2020-2024 Rocket 3 motorcycles because the rear brake master cylinder may fail to move fluid properly, requiring an extended distance to stop. 3,557 units affected.

    Product
    TRIUMPH — TRIUMPH ROCKET 3 R, ROCKET 3 GT, ROCKET 3 TFC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23T007000·2023-10-31

    Toyo Recalls Open Country and Extensa Tires Due to Mold Defect

    Toyo Tire Holdings is recalling certain Open Country and Extensa tires because they may have been produced with the wrong mold, risking tread or sidewall detachment.

    Product
    TIRES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V726000·2023-10-30

    Starcraft and Glaval Transit Buses Recalled for Air Compressor Defect

    Forest River Bus is recalling certain 2021-2023 Starcraft and Glaval transit buses because the air conditioning compressor may contact the sway bar, risking loss of steering control.

    Product
    STARCRAFT BUS — STARCRAFT BUS, GLAVAL BUS ALLSTAR XL, ALLSTAR XLT, CONCORDE II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·054-2023·2023-10-30

    Olymel Recalls Ready-to-Eat Ham Products Imported Without Reinspection

    Olymel is recalling approximately 11,016 pounds of ready-to-eat ham products that were imported into the United States without the required import reinspection.

    Product
    Olymel Recalls Ready-To-Eat Ham Products Imported Without the Benefit of Import Reinspection
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·23V727000·2023-10-27

    Ford Mustang Brake Fluid Warning System Software Recall

    Ford is recalling 2020-2023 Mustang vehicles because the brake fluid level sensor may fail to illuminate the warning light when brake fluid is low. Drivers could operate the vehicle with insufficient brake fluid, reducing braking performance and increasing crash risk.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V722000·2023-10-26

    New Flyer Transit Buses Recalled for Transmission Yoke Separation Risk

    New Flyer is recalling 2019-2024 transit buses because the transmission yoke may separate, causing a sudden loss of drive power and increasing crash risk.

    Product
    NEW FLYER — NEW FLYER XN40, XN35, XD35, XD40
    Category
    Vehicle
    Distribution
    Distributed nationwide