The Recall Desk

State

California product recalls

72,986 recalls have nationwide distribution and so reach California. 13,247 additional recalls listed California specifically in their distribution scope.

What the numbers show

Total
13,247
Critical
1,605
Severe
2,844
Most recent
2026-09-25

Of the 13,247 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 2,844 (21%) are Severe.

These figures cover only the 13,247 recalls whose distribution notice names California specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8326–8350 of 86233

  • ModerateFDA (Devices)·Z-1252-2025·2025-03-12

    Philips IntelliSpace Cardiovascular Software Data Archival Failure Recall

    Philips cardiovascular diagnostic software version 7.0.0.0 cannot archive, copy, or export study data, affecting 139 units distributed nationwide. Users may experience data management and workflow disruptions.

    Product
    Philips IntelliSpace Cardiovascular software, Model 830089.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0603-2025·2025-03-12

    Noble Made Garlic Parmesan Wing Sauce recalled for foaming issue

    Noble Made Garlic Parmesan Wing Sauce is being recalled due to customer complaints of bottles foaming when opened. The product was distributed to retail locations across multiple states.

    Product
    Noble Made Garlic Parmesan Wing Sauce, net wt 9.25oz, UPC 850000398542, #0897 BEST BY 06/02/2026 14:02 33724 L1, Code: F20920061
    Category
    Food
    Distribution
    18 states
  • ModerateFDA (Drugs)·D-0251-2025·2025-03-12

    Simethicone Oral Syringe Recalled for Defective Delivery System

    Safecor Health is recalling Simethicone 20 mg oral syringes due to leakage caused by a defective delivery system. Approximately 10,992 syringes were distributed nationwide.

    Product
    Simethicone 20 mg per 0.3 mL Oral Syringe, Delivers: 0.3 mL, Oral Drops, Mfg By: Rugby, Pkg by: Safecor Health, LLC, Columbus, OH 43204, NDC: 00536130375.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1251-2025·2025-03-12

    Infiltration Cannula Recalled Due to Incorrect Water Jet Pattern

    HUMAN MED AG is recalling 775 Biofill Infiltration Cannulas because the water jet may emerge as a spot jet rather than the specified fan-shaped spray pattern, affecting device functionality.

    Product
    human med Biofill Infiltration Cannula, diameter 2.5mm, 15cm, REF 2024-012, REF 1580107, sterile, single use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1271-2025·2025-03-12

    Dental implant abutments recalled for incorrect packaging labels

    Hiossen has recalled ET Rigid Abutment dental implant components because stickers in the packaging mislabel whether products are Mini or Regular versions. Incorrect identification could affect proper implant installation.

    Product
    ET Rigid Abutment (Mini) Size 4.5D 1.0G/H 5.0H - Intended for use with a dental implant to provide support for prosthetic restorations such as crowns, bridges, or overdentures. GA4515MP Model/Catalog Number: ETRGA4515MP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0250-2025·2025-03-12

    Vitamin D Supplement Oral Syringes Recalled for Defective Delivery System

    Safecor Health is recalling 3069 units of Ergocalciferol (Vitamin D Supplement) oral syringes nationwide due to leakage in the repackaged unit-dose delivery system. No illnesses have been reported.

    Product
    Ergocalciferol - Vitamin D Supplement - 10 mcg (400 Units) per 0.05 mL Oral Syringe, Delivers: 0.05 mL Oral Solution, Mfg by: Westminster, Pkg by: Safecor Health, LLC, Columbus, OH 43204, NDC: 69367028302.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0643-2025·2025-03-12

    Orgeat Almond Syrup Recalled Due to Potential Yeast Contamination

    A C Calderoni & Co. Inc. is recalling Orgeat Almond Syrup due to potential yeast contamination in the product. The affected product was distributed to foodservice distributors and restaurants in California.

    Product
    ORGEAT ALMOND SYRUP; 32 fl oz (946 ml); Glass bottle with screw-top lid; Contains: Sugar, Water, Citric Acid Natural Flavor, Sodium Benzoate; Refrigerate after opening
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1272-2025·2025-03-12

    Dental abutment implants recalled for incorrect patient chart stickers

    Hiossen Inc. is recalling ET Rigid Abutment (Mini) dental implant components due to patient chart stickers that incorrectly identify the product version. The stickers may identify Mini versions as Regular, or Multi-versions as Mini.

    Product
    ET Rigid Abutment (Mini) SIze: 4.5D 3.0G/H 7.0H - Intended for use with a dental implant to provide support for prosthetic restorations such as crowns, bridges, or overdentures. Model/Catalog Number: ETRGA4537MP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1296-2025·2025-03-12

    BD BBL TB Stain Kit Expiration Date Labeling Discrepancy

    BD BBL TB Stain Kit component shipped with incorrect expiration date labeling. One component has printed expiration 30 September 2024 while Certificate of Analysis indicates 30 April 2025, creating confusion about product validity.

    Product
    BD BBL TB Stain Kit K, Catalog (REF): 212522
    Category
    Medical Device
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-1292-2025·2025-03-12

    Vios bedside monitor batteries may deplete during storage

    Murata Vios bedside monitors may experience battery depletion if stored without power, causing tablet connectivity issues. Affected units should be kept plugged in while in storage.

    Product
    Vios Monitoring System Bedside Monitor Model BSM2050
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1275-2025·2025-03-12

    ET Rigid and Multi Dental Abutments Recalled for Incorrect Identification Stickers

    Hiossen recalled ET Rigid and Multi dental abutments for incorrect identification stickers in packaging that misidentify product versions, risking improper placement during installation.

    Product
    ET Rigid Abutment (Mini) Size: 4.5D 2.0G/H 4.0H- Intended for use with a dental implant to provide support for prosthetic restorations such as crowns, bridges, or overdentures. Model/Catalog Number: ETRGA4524MP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E017000·2025-03-11

    Meyle Recalls Front Control Arms Due to Manufacturing Defect

    Meyle AG is recalling specific front control arms that may fail due to a manufacturing defect, potentially causing loss of steering and control.

    Product
    SUSPENSION:FRONT:CONTROL ARM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V153000·2025-03-11

    Nissan Sentra driver seat frames may not be fully secured

    Nissan is recalling certain 2025 Sentra vehicles because the driver's seat frame may not be fully secured to the outer side of the seat track, failing FMVSS 207 and 210.

    Product
    NISSAN — NISSAN SENTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V151000·2025-03-11

    Keystone travel trailer wiring lacks sufficient surge protection

    Keystone RV is recalling certain 2025 Kodiak, Colorado and Sunset travel trailers because the 7-way cord and 12-volt distribution box were wired with insufficient surge protection.

    Product
    KEYSTONE — KEYSTONE KODIAK, COLORADO, SUNSET TRAIL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V150000·2025-03-07

    Mercedes-Benz Recalls 2023 EQE Models for Detaching Wheel Rim Inserts

    Mercedes-Benz is recalling 2023 EQE 350 4MATIC and EQE 350+ vehicles because wheel rim inserts may detach while driving, creating a crash hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ redundant EQE 350 4MATIC, EQE 350+
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V149000·2025-03-07

    2025 Forest River Aurora Travel Trailers Electrical Fire Risk Recall

    Forest River is recalling certain 2025 Aurora ART26BHS travel trailers because the air conditioner electrical connector may have exposed wiring strands that can cause electrical arcing and fire.

    Product
    FOREST RIVER — FOREST RIVER AURORA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25160·2025-03-06

    Nuby Stroller Fans recalled due to laceration injury hazard

    Nuby Stroller Fans are recalled because the housing allows children's fingers to contact the spinning blade, causing lacerations; six injuries have been reported. Consumers should stop using the product immediately and contact the manufacturer for a free replacement.

    Product
    Nuby Stroller Fans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25168·2025-03-06

    Children's Nightgowns and Robes Recalled for Flammability and Burn Hazard

    Marie-Chantal children's nightgowns, pajama sets and robes violate federal flammability standards for sleepwear, posing a risk of serious burn injuries. About 560 units sold nationwide from November 2021 through October 2024; consumers should stop use immediately.

    Product
    Marie-Chantal Children's Nightgowns, Pajama Sets and Robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25170·2025-03-06

    Auto World Unassembled Slot Cars Recalled for Loose Magnet Ingestion Hazard

    About 55,000 Auto World Unassembled Deluxe Pit Kit Slot Cars are being recalled because loose magnets in unassembled kits pose an ingestion hazard to children. The products were sold nationwide from July 2023 to February 2024.

    Product
    Auto World Unassembled Deluxe Pit Kit Slot Cars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·25172·2025-03-06

    Love Our Home Crib Bumpers Recalled for Federal Ban Violation and Suffocation Risk

    Love Our Home braided crib bumpers sold on Shein.com violate the federal Safe Sleep for Babies Act and pose a suffocation hazard to infants. About 750 units were sold between March and November 2024.

    Product
    Love Our Home Braided Crib Bumpers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·25V145000·2025-03-06

    Jayco Recalls 2024-2025 Motorhomes Due to Incorrect Federal Load Labels

    Jayco is recalling specific 2024 and 2025 motorhomes because incorrect Federal labels may allow the vehicles to be overloaded, increasing crash risk.

    Product
    ENTEGRA — ENTEGRA, JAYCO CONDOR, ALANTE SE, REDHAWK SE, ODYSSEY SE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V146000·2025-03-06

    2024 Kawasaki Z500 and Ninja 500 Motorcycles Clutch Release Shaft

    Kawasaki is recalling certain 2024 Z500 and Ninja 500 motorcycles due to improper welding of the clutch release shaft, which can cause the clutch lever to break and disable the motorcycle, increasing crash risk.

    Product
    KAWASAKI — KAWASAKI NINJA 500, Z500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·25173·2025-03-06

    Taylor Water Technologies Recalls Phosphate Reagent Bottles Due to Chemical Burn Risk

    Taylor Water Technologies is recalling about 10,000 Phosphate Reagent #1 bottles sold with test kits. The sulfuric acid bottles lack required child-resistant packaging, posing a risk of severe chemical burns.

    Product
    Phosphate Reagent #1 Bottles sold within the Taylor Phosphate Test Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide