The Recall Desk

State

California product recalls

73,088 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 73,088 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9476–9500 of 86339

  • SevereFDA (Food)·F-0273-2025·2024-12-18

    Vegetable Medley Recalled for Potential E. coli Contamination

    4 Earth Farms is recalling its 32-oz Vegetable Medley product distributed by Walmart due to potential contamination with E. coli O121:H19. The product was distributed to retail locations across multiple states.

    Product
    Vegetable Medley; Broccoli, Cauliflower, Carrots. Washed and ready to prepare; Perishable keep refrigerated. NET WT 32 OZ (2 LB) 907g DISTRIBUTED BY: Walmart Inc., Bentonville, AR 78716
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-0271-2025·2024-12-18

    Mediterranean Party Tray Recalled for Potential Salmonella Contamination

    F&S Produce West LLC is recalling Mediterranean Party Trays (sell-by dates 11/27/2024–12/11/2024) due to potential Salmonella contamination in the tzatziki sauce. The product was distributed to 187 retail locations in seven western states.

    Product
    Mediterranean Inspired Party Tray; Sell by dates 11/27/2024- 12/11/2024 UPC: 826766145966; Perishable, Keep Refrigerated
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-0277-2025·2024-12-18

    Organic Vegetable Medley Recalled for Potential E. Coli O121 Contamination

    4 Earth Farms is recalling Organic Vegetable Medley packages due to potential contamination with E. coli O121:H19. The affected products were distributed across multiple states to distribution centers and retailers.

    Product
    Organic Vegetable Medley; Broccoli, Cauliflower, & Carrots. Washed and ready to prepare; Perishable keep refrigerated. NET WT 12 OZ (340g) (6 pack/case) DISTRIBUTED BY: UNFI, Providence, RI 02908 USA
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-0274-2025·2024-12-18

    Vegetable Medley Recalled for Potential E. coli O121:H19 Contamination

    4 Earth Farms is recalling Vegetable Medley due to potential contamination with E. coli O121:H19. Approximately 6,036 cases were distributed across multiple states.

    Product
    Vegetable Medley; Broccoli, Cauliflower, Carrots. Washed and ready to prepare; Perishable keep refrigerated. NET WT 12 OZ (340g) (6 pack/case) DISTRIBUTED BY: Walmart Inc., Bentonville, AR 78716
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-0280-2025·2024-12-18

    Organic Carrots Recalled for Potential E. coli O121:H19 Contamination

    4Earth Farms is recalling 6,036 cases of organic carrots distributed across multiple states due to potential E. coli O121:H19 contamination.

    Product
    Organic Carrots. Bulk 1 pound bags. Washed and ready to prepare, Perishable keep refrigerated. Distributed by 4Earth Farms, LLC., Commerce, CA 92022 USA
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-0276-2025·2024-12-18

    Organic Vegetable Medley Recalled for E. coli O121 Contamination Risk

    4 Earth Farms is recalling Organic Vegetable Medley (Broccoli, Carrots & Cauliflower) sold at Walmart due to potential contamination with E. coli O121:H19. The recall affects 6,036 cases distributed across multiple states.

    Product
    Organic Vegetable Medley; Broccoli, Carrots & Cauliflower. Washed and ready to prepare; Perishable keep refrigerated. NET WT 12 OZ (340g) (6 pack/case) DISTRIBUTED BY: Walmart Inc., Bentonville, AR 78716
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-0678-2025·2024-12-18

    Hermes Medical Imaging Software May Cause Incorrect Image Reconstruction

    Hermes Medical Solutions is recalling Hybrid Recon software (versions 4.0.0x and 5.0.0) due to a potential software configuration issue that may cause incorrect alignment during SPECT/CT image reconstruction. The issue affects 778 systems in the U.S. and internationally.

    Product
    Hybrid Recon software on Hermes Medical Imaging Suite version 6.1 Hybrid Recon software versions affected are 4.0.0x and 5.0.0
    Category
    Medical Device
    Distribution
    15 states
  • HighFDA (Drugs)·D-0118-2025·2024-12-18

    Drug Recall: Levothyroxine Sodium Tablets Affected by Potency Failures

    Viatris Inc recalls 92,512 bottles of Levothyroxine Sodium tablets with potency failures—some are stronger than intended, others are weaker than intended.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0131-2025·2024-12-18

    Levothyroxine Sodium 100 mcg Tablets Recalled for Potency Deviations Nationwide

    Mylan Institutional is recalling 2,835 cartons of Levothyroxine Sodium 100 mcg tablets nationwide due to potency deviations—some tablets may be underdosed while others may be overdosed.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0135-2025·2024-12-18

    FDA Recalls Levothyroxine Sodium Tablets for Potency Variation

    Mylan Institutional recalls 690 cartons of Levothyroxine Sodium 150 mcg tablets nationwide due to potency variation. Some units may be subpotent or superpotent.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0267-2025·2024-12-18

    Dried Cinnamon Powder Recalled for Elevated Lead Contamination

    Super Brand Dried Cinnamon Powder (4 oz) distributed across nine states is being recalled due to elevated lead levels. Consumers should discard purchased containers.

    Product
    "***SUPER***BRAND***DRIED CINNAMON POWDER***Net Wt: 4oz(113g)***PRODUCT OF CHINA***DISTRIBUTOR: IHA BEVERAGE COMMERCE, CA, 90040***"UPC#610232012476
    Category
    Food
    Distribution
    9 states
  • HighFDA (Drugs)·D-0121-2025·2024-12-18

    Levothyroxine Sodium Tablets recalled nationwide for potency failures

    Viatris Inc. is recalling 19,549 bottles of Levothyroxine Sodium 175 mcg tablets nationwide due to potency failures. Some tablets contain excessive active ingredient while others contain insufficient amounts.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·24V941000·2024-12-18

    2025 Mercedes-Benz E-Class vehicles recalled for rear axle carrier defect

    Mercedes-Benz is recalling 2025 E 350, E 350 4MATIC, E 450 4MATIC, and E 450 4MATIC station wagon vehicles due to an improperly welded camber strut bracket on the rear axle carrier that may separate and cause loss of vehicle handling and control.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 450 4MATIC ALL-TERRAIN, E 350, E 450 4MATIC, E 350 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0262-2025·2024-12-18

    Dietary supplement recalled for undeclared soy lecithin allergen

    DesBio lunaSOMM Natural Sleep Support Dietary Supplement is recalled due to undeclared soy lecithin. The product is labeled as containing sunflower lecithin but contains soy lecithin, posing a risk to consumers with soy allergies.

    Product
    DesBio lunaSOMM Natural Sleep Support Dietary Supplement capsules, 30 count in a Blue PET bottle with a White cap. Supplement facts declare Phosphatidylserine (from non-GMO sunflower lecithin powder) 40 mg. Distributed by Deseret Biologicals Inc 469 West Parkland Dr, Sandy, UT.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0136-2025·2024-12-18

    Levothyroxine Sodium Tablets Recalled for Subpotent and Superpotent Content

    Mylan Institutional is recalling Levothyroxine Sodium tablets nationwide due to subpotent and superpotent units. Patients taking affected tablets may receive incorrect doses of this thyroid medication.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0124-2025·2024-12-18

    Levothyroxine Sodium Tablets Recalled for Potency Variation and Dosage Failures

    Viatris Inc. is recalling 42,331 bottles of Levothyroxine Sodium Tablets 50 mcg distributed nationwide due to potency failures resulting in both superpotent and subpotent tablets.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0127-2025·2024-12-18

    Levothyroxine sodium tablets recalled for potency failures nationwide

    Viatris Inc is recalling Levothyroxine Sodium 100 mcg tablets for potency failures causing some tablets to be too strong and others too weak. Approximately 65,169 units are affected nationwide.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0674-2025·2024-12-18

    Convertor Isolation Gowns may fail protective barrier requirements

    Cardinal Health is recalling 940,203 Convertor Isolation Gowns because raw materials may prevent them from meeting AAMI Level 3 protection specifications.

    Product
    Convertor Isolation Gown, AAMI Level 3 protection, Product Codes AT6100, AT6100-XL, AT6200, and AT6200-XL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V938000·2024-12-18

    Volvo Recalls 2023-2024 C40 Vehicles for Air Bag Clamp Defect

    Volvo is recalling 2023-2024 C40 vehicles because improperly crimped clamps may cause the driver's air bag to deploy improperly, increasing injury risk.

    Product
    VOLVO — VOLVO C40BEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V937000·2024-12-18

    2025 Chevrolet Silverado EV Pedestrian Alert System Sound Volume

    General Motors is recalling certain 2025 Chevrolet Silverado EV work trucks because the pedestrian alert sound system may not produce sound at sufficient volume. This increases the risk of pedestrians being unaware of an approaching vehicle.

    Product
    CHEVROLET — CHEVROLET SILVERADO EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0126-2025·2024-12-18

    Levothyroxine Sodium Tablets Recalled Due to Potency Failures

    Viatris Inc recalls 43,765 bottles of Levothyroxine Sodium 88 mcg tablets nationwide due to potency failures where some tablets are stronger and others weaker than labeled.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0120-2025·2024-12-18

    Levothyroxine sodium tablets recalled for potency failures nationwide

    Viatris Inc is recalling Levothyroxine Sodium Tablets USP 150 mcg nationwide due to potency failures. Affected lots containing both subpotent and superpotent tablets expire June 2025.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0134-2025·2024-12-18

    Levothyroxine Sodium Tablets Recalled Nationwide for Potency Variance

    Mylan Institutional recalls 1,133 cartons of Levothyroxine Sodium Tablets (137 mcg) nationwide. Three lots contain subpotent and superpotent tablets.

    Product
    LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0130-2025·2024-12-18

    Prescription drug Dabigatran Etexilate recalled for elevated nitrosamine impurity

    Ascend Laboratories is recalling Dabigatran Etexilate 150mg capsules due to elevated N-nitroso-Dabigatran impurity from a manufacturing deviation. Affected lots were distributed nationwide; consult your physician before making changes to your medication.

    Product
    DABIGATRAN ETEXILATE — DABIGATRAN ETEXILATE (DABIGATRAN ETEXILATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0129-2025·2024-12-18

    Dabigatran Etexilate 75 mg capsules recalled for N-nitroso impurity

    Ascend Laboratories is recalling Dabigatran Etexilate 75 mg capsules nationwide due to manufacturing deviations. Three lots contain N-nitroso-Dabigatran impurity above recommended interim limits.

    Product
    DABIGATRAN ETEXILATE — DABIGATRAN ETEXILATE (DABIGATRAN ETEXILATE)
    Category
    Drug
    Distribution
    Distributed nationwide