The Recall Desk

State

California product recalls

73,218 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.

These figures cover only the 13,255 recalls whose distribution notice names California specifically. The 73,218 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15026–15050 of 86473

  • SevereFDA (Devices)·Z-0541-2024·2023-12-27

    AirFit F30 Full Face Mask recalled for magnetic interference with medical implants

    ResMed is recalling the AirFit F30 Full Face Mask because the device contains magnets that can interfere with active medical implants and ferromagnetic objects. The original user guide did not adequately warn about safe distance requirements.

    Product
    AirFit F30 Full Face Mask and User Guide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0151-2024·2023-12-27

    TING 2% Miconazole Nitrate Spray Recalled for Benzene Contamination

    Insight Pharmaceuticals recalls TING 2% Miconazole Nitrate Athlete's Foot Spray due to benzene contamination. The recall affects 117,336 cans distributed nationwide and in Puerto Rico.

    Product
    TING 2% Miconazole Nitrate Athlete's Foot Spray Antifungal Spray Powder, NET WT 4.5 oz (128 g) cans, Distributed by: Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company, Tarrytown, NY 10591, UPC 363736532611.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0159-2024·2023-12-27

    Blistex Tolnaftate antifungal spray powder recalled for benzene contamination

    Blistex Inc is recalling Odor-Eaters brand Tolnaftate 1% antifungal spray powder nationwide due to benzene contamination. The recall affects approximately 243,386 cases distributed in the USA, Canada, and Korea.

    Product
    BLISTEX — BLISTEX (TOLNAFTATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0645-2024·2023-12-27

    HMC Farms Plums Recalled Due to Potential Listeria Contamination

    The HMC Group Marketing Inc is recalling HMC Farms Plums 2lb Gusset Bags (UPC 788814320858) due to potential contamination with Listeria monocytogenes. The product was distributed throughout the United States and internationally.

    Product
    HMC Farms Plums 2lb Gusset Bag
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Devices)·Z-0512-2024·2023-12-27

    Sodium Chloride IV Flush Kits Recalled for Potential Sterility Failure

    Nurse Assist recalls sodium chloride IV flush solutions due to potential loss of sterility assurance. Nonsterile solutions could cause infection when used for intravenous administration.

    Product
    0.9% Sodium Chloride: Product Name/Product Code: 10ML IV FLUSH STERILE FIELD/EMZ10091240
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0511-2024·2023-12-27

    IV Flush Syringes and Irrigation Solutions Recalled for Sterility Defect

    Nurse Assist, LLC recalls sodium chloride irrigation solutions and IV flush syringes due to potential lack of sterility assurance, which could allow contamination and infections.

    Product
    0.9% Sodium Chloride: Brand Name: Product Name/Product Code: MAC MEDICAL: 10ML FILL SYRINGE/9210; NURSE ASSIST: 3ML IV FLUSH SYRINGE/1203-BP, 5ML IV FLUSH SYRINGE/1205-BP, 10ML IV FLUSH SYRINGE/1210-BP; SOL: 0.9% SODIUM CHLORIDE IV FLUSH SYRINGE/PFF001; HALYARD OWENS MINOR…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0646-2024·2023-12-27

    HMC Farms White Peaches recalled due to potential Listeria contamination

    HMC Farms White Peaches 2lb Gusset Bag are recalled due to potential Listeria monocytogenes contamination. The product was distributed across the United States and internationally.

    Product
    HMC Farms White Peaches 2lb Gusset Bag
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Food)·F-0651-2024·2023-12-27

    HMC Farms Peaches Recalled for Potential Listeria Contamination

    HMC Farms Peaches in 4lb boxes are being recalled due to potential contamination with Listeria monocytogenes. The product was distributed to 26 U.S. states and three countries.

    Product
    HMC Farms Peaches 4lb box
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Food)·F-0652-2024·2023-12-27

    HMC Farms White Nectarines Recalled for Potential Listeria Contamination

    HMC Farms White Nectarines 4lb boxes are being recalled due to potential contamination with Listeria monocytogenes. The product was distributed to 26 U.S. states and internationally.

    Product
    HMC Farms White Nectarines 4lb box
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Devices)·Z-0542-2024·2023-12-27

    AirFit F30i Full Face Mask Recalled Due to Magnetic Interference Risk

    ResMed is recalling the AirFit F30i Full Face Mask due to potential magnetic interference with active medical implants and ferromagnetic objects. Safety warnings are being updated.

    Product
    AirFit F30i Full Face Mask and User Guide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0549-2024·2023-12-27

    Infusion pump recalled for mechanical valve interference interrupting therapy delivery

    Ivenix infusion pump may experience mechanical interference on fluid valve pins, interrupting therapy delivery. FDA recalled 938 units in five states due to potential risk of serious patient harm.

    Product
    Ivenix Infusion System (IIS), Large Volume Pump LVP-0004
    Category
    Medical Device
    Distribution
    5 states
  • SevereFDA (Food)·F-0608-2024·2023-12-27

    Dark Chocolate Coins Recalled for Undeclared Milk Allergen

    Manischewitz Magic Max's Dark Chocolate Coins are recalled due to undeclared milk from mispackaging. The product was distributed to retailers in multiple states and may affect consumers with milk allergies.

    Product
    Manischewitz Magic Max's Dark Chocolate Coins, NET WT. 0.53 OZ (15g), UPC: 072700200387 Display Box UPC: 072700200356, 12 bags per case. Product packaged in gold foil in blue netting bags.
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·F-0647-2024·2023-12-27

    HMC Farms White Nectarines recalled due to potential Listeria contamination

    HMC Farms White Nectarines 2lb Gusset Bags are recalled due to potential contamination with Listeria monocytogenes. The affected product was distributed across the United States and internationally.

    Product
    HMC Farms White Nectarines 2lb Gusset Bag
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Food)·F-0648-2024·2023-12-27

    HMC Farms Peaches Recalled Due to Listeria Contamination Risk

    HMC Farms Peaches Signature Farms 2lb bags have been recalled due to potential Listeria monocytogenes contamination. The affected product was distributed widely across the United States and internationally.

    Product
    HMC Farms Peaches Signature Farms 2lb bag
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Devices)·Z-0538-2024·2023-12-27

    AirTouch F20 Full Face Mask Recalled for Magnetic Interference with Medical Implants

    ResMed recalls 3.8 million AirTouch F20 full face masks with magnets that may interfere with active medical implants. Updated safety warnings regarding safe distances from medical devices are being issued.

    Product
    AirTouch F20 Full Face Mask and User Guide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0650-2024·2023-12-27

    HMC Farms Nectarines Recalled Due to Listeria Contamination Risk

    HMC Farms Nectarines 4lb bags are recalled due to potential Listeria monocytogenes contamination. The recall affects 26 US states, Mexico, Canada, and Taiwan.

    Product
    HMC Farms Nectarines 4lb bag
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Devices)·Z-0515-2024·2023-12-27

    Sterile Water Syringes recalled for lack of sterility assurance

    Nurse Assist LLC recalls sterile water injection and irrigation syringes for inadequate sterility assurance. Affected products may be nonsterile and could cause infection if used.

    Product
    Sterile Water: Product Name/Product Code: USP STERILE WATER SYRINGE/1030A, SYRINGE PREFILLED 10 ML/6496722, 30CC PREFILLED SYRINGE/6496723, USP STERILE WATER SYRINGE/1030, 10CC PREFILLED SYRINGES/51638, 30CC PREFILLED SYRINGES/52333, 10CC PREFILLED SYRINGES/1010
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0539-2024·2023-12-27

    AirFit N20 Nasal Mask: Magnetic Interference with Medical Implants

    ResMed AirFit N20 Nasal Masks contain magnets that may interfere with active medical implants and ferromagnetic objects. The FDA classified this as Class I; ResMed is updating safety warnings with required distances.

    Product
    AirFit N20 Nasal Mask and User Guide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0608-2024·2023-12-27

    RAPIDPoint 500 Measurement Cartridge Sodium Sensor May Cause Measurement Error

    Siemens RAPIDPoint 500 cartridges may produce inaccurate sodium measurements in blood samples, potentially delaying diagnosis or causing inappropriate treatment. The sodium sensor may show a negative bias, affecting patient care.

    Product
    RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 400-Intended for in vitro diagnostic use and is designed to provide the determination in whole blood. SMN: 10491448
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0589-2024·2023-12-27

    Acrobat-i Vacuum Positioner System Recalled for Positioner Arm Locking Failure

    Maquet Cardiovascular is recalling the Acrobat-i Vacuum Positioner System because the positioner arm may fail to tighten or lock during normal use, which could affect surgical positioning.

    Product
    Acrobat-i Vacuum Positioner System, Model Number XP-5000Z
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0609-2024·2023-12-27

    RAPIDPoint 500 Measurement Cartridge Sodium Sensor Negative Bias Risk

    Siemens RAPIDPoint 500 measurement cartridges may produce inaccurate sodium readings, risking delayed diagnosis of dangerous electrolyte imbalances or unnecessary treatment.

    Product
    RAPIDPoint 500 Systems Measurement Cartridge (with Lactate) 750-Intended for in vitro diagnostic use and is designed to provide the determination in whole blood. SMN: 10491449
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0559-2024·2023-12-27

    Philips Azurion Ceiling-Mount Systems Rotation Cover May Fall

    Philips is recalling Azurion ceiling-mount imaging systems because a rotation cover may fall if the L-arm collides with hospital equipment, potentially causing injury or affecting sterilization.

    Product
    Philips Azurion systems with monoplane fixed ceiling mounts: 722078 Azurion 7 M12 722079 Azurion 7 M20 722223 Azurion 7 M12 722224 Azurion 7 M20 722227 Azurion 5 M12 722228 Azurion 5 M20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0567-2024·2023-12-27

    AC Power Adapter for LIFEPAK 15 Defibrillator May Fail to Charge or Power On

    AC power adapters for LIFEPAK 15 Monitor/Defibrillators may fail to charge batteries or power on the device. Physio-Control is recalling 18,732 units manufactured between November 2021 and April 2023.

    Product
    AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0576-2024·2023-12-27

    Philips Inclusive CT Systems: Software Errors in Image Display and Interpretation

    Philips North America is recalling 330 Philips Inclusive CT imaging systems due to software issues causing incorrect image display, errors in image interpretation, and patient exposure to incorrect images and system functions during clinical use.

    Product
    The device is a whole-body CT x-ray system. The acquired x-ray transmission data is reconstructed by computer into cross-sectional images of the body taken at different angles and planes. The system also includes signal analysis and display equipment, patient and equipment…
    Category
    Medical Device
    Distribution
    25 states