The Recall Desk

State

California product recalls

72,936 recalls have nationwide distribution and so reach California. 13,245 additional recalls listed California specifically in their distribution scope.

What the numbers show

Total
13,245
Critical
1,605
Severe
2,843
Most recent
2026-09-09

Of the 13,245 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 2,843 (21%) are Severe.

These figures cover only the 13,245 recalls whose distribution notice names California specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3251–3275 of 86181

  • HighCPSC·26292·2026-02-26

    TheKiddoSpace Recalls Children's Story Books Due to Choking Hazard

    TheKiddoSpace is recalling about 140 children's story books because felt parts can detach and pose a choking hazard. No injuries have been reported.

    Product
    TheKiddoSpace Children's Story Books
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26293·2026-02-26

    TheKiddoSpace Recalls Children's Handwriting Kits Over Lead Exposure

    TheKiddoSpace is recalling about 19,700 children's handwriting practice kits because the pens contain lead levels that violate the federal lead content ban. No injuries have been reported.

    Product
    TheKiddoSpace Print and Cursive Handwriting Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26304·2026-02-26

    Concord Rechargeable Light-Up Bike Helmets Recalled Due to Head Injury Risk

    Todson is recalling about 40,245 Concord 360 Degree Rechargeable Light-Up Bike Helmets because they fail to meet safety standards, posing a risk of serious head injury or death.

    Product
    Concord 360 Degree Rechargeable Light-Up Bike Helmet
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26295·2026-02-26

    TheKiddoSpace Recalls Reusable Water Balloons Over Phthalate Ban Violation

    TheKiddoSpace is recalling about 4,300 reusable water balloons because the cord lock on the storage bag contains a regulated phthalate that violates the federal phthalate ban. No injuries have been reported.

    Product
    TheKiddoSpace Reusable Water Balloons
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26307·2026-02-26

    Babysense Max View Baby Monitors Recalled Over Fire Hazard

    About 81,800 Babysense Max View baby monitors are recalled because the display unit can overheat and spark while charging, creating a fire hazard. Hisense has received 11 incident reports with no injuries reported.

    Product
    Babysense Max View Baby Monitors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26289·2026-02-26

    Magnetic Chess Games Recalled Over Magnet Ingestion Risk

    Magnetic chess games sold on Amazon by Kaiwenshangpin are recalled because loose magnets inside can be swallowed by children, potentially causing intestinal damage or death. No injuries have been reported.

    Product
    Magnetic Chess Games
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V112000·2026-02-26

    Honda Prologue and Acura ZDX instrument and camera displays may fail

    Honda is recalling certain 2024 Acura ZDX and Prologue vehicles because a software error may cause the instrument panel display to fail and the rearview camera to show a blank screen in reverse.

    Product
    ACURA — ACURA, HONDA ZDX, PROLOGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·26305·2026-02-26

    SumDirect LED Mini Lights Recalled Over Battery Ingestion Hazard

    SumDirect LED Mini Lights are recalled because the button cell batteries can be easily accessed by children, posing an ingestion hazard. No injuries have been reported.

    Product
    SumDirect LED Mini Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26302·2026-02-26

    Zelbuck Magnetism Ball Game Toys Recalled Due to Ingestion Hazard

    Zelbuck Magnetism Ball Game Toys are being recalled because they contain loose magnets that pose a serious injury or death risk if swallowed.

    Product
    Zelbuck Magnetism Ball Game Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26264·2026-02-26

    Vevor Retractable Baby Gates Recalled Due to Entrapment Hazard

    Sanven Technology is recalling approximately 10,400 Vevor Retractable Baby Gates because they violate safety standards and pose an entrapment risk to children.

    Product
    Vevor Retractable Baby Gates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26298·2026-02-26

    TheKiddoSpace Recalls LED Soccer Hover Balls Due to Burn Hazard Risk

    TheKiddoSpace is recalling approximately 650 LED soccer hover balls because the battery surface temperature can exceed safety limits, posing a burn risk.

    Product
    TheKiddoSpace LED Soccer Hover Balls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V115000·2026-02-26

    BMW Recalls One 2026 S 1000 RR Motorcycle for Turn Signal Defect

    BMW is recalling one 2026 S 1000 RR motorcycle because the turn signal reset button can be unintentionally activated, causing the turn signal to fail.

    Product
    BMW — BMW S 1000 RR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V114000·2026-02-26

    General Motors Vehicles Recalled for Missing Electronic Owner's Manual

    General Motors has recalled multiple Chevrolet, GMC, Cadillac, and Buick vehicles from 2025–2027 because their radios were not properly configured to download the electronic owner's manual during production. Without the manual, owners may not know how to safely operate the vehicle.

    Product
    CHEVROLET — CHEVROLET, CADILLAC, BUICK SILVERADO 2500, SILVERADO 3500, BLAZER EV, VISTIQ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0517-2026·2026-02-25

    Tuna salad recalled after being mislabeled with a chicken salad lid

    Reser's Fine Foods is recalling 298 tubs of tuna salad that were mislabeled with a Molly Kitchen's Chicken Salad lid, leaving fish undeclared.

    Product
    The Tuna Salad product container is mislabeled with a Chicken Salad lid, which states: Molly Kitchen's Chicken Salad, 789953, NET WT. 5 LB (2.26 kg) per plastic tub. UPC 7 5810830149 8. Distributed by US Foods, Inc. Rosemont, IL 60018. The lid declares Contains: Eggs, Milk, Wheat
    Category
    Food
    Distribution
    5 states
  • CriticalFDA (Food)·H-0514-2026·2026-02-25

    Brass cooking pot recalled over potential contamination with leachable lead

    Lotus Mom Corporation is recalling 9 units of a 4-quart Brass Pital Pot over potential contamination with leachable lead.

    Product
    Brass Pital Pot 4-quart. Sticker label: BRASS HAMMERED HANDI NO 3 UPC 7 023672 414398 US $ 74.99 Sticker label: IKM INDIAN KITCHEN MART
    Category
    Food
    Distribution
    2 states
  • CriticalFDA (Devices)·Z-1353-2026·2026-02-25

    Olympus High Flow Insufflation Unit Model UHI-2 Recalled Due to Software Issue

    Olympus Corporation of the Americas is recalling 744 Olympus High Flow Insufflation Units (Model UHI-2) because a software algorithm issue may cause overpressure events.

    Product
    Olympus High Flow Insufflation Unit. Model/ Number: UHI-2. Used for insufflation of the abdominal cavity, and automatic suction and smoke evacuation to facilitate laparoscopic observation and treatment within the abdominal cavity.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0510-2026·2026-02-25

    Moringa capsules recalled over potential contamination with Salmonella

    Art Monkey LLC is recalling 8,500 bottles of Why Not Natural Moringa Capsules because they have the potential to be contaminated with Salmonella.

    Product
    Why Not Natural Moringa Capsules 120 capsule bottle marked with lot # A25G051 on the bottom and with an expiration date of 07/2028 stamped on the bottom.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1387-2026·2026-02-25

    Medline Nerve Block Trays Recalled Over Sterilization Calibration Issues

    Medline is recalling 448 units of its BASIC NERVE BLOCK TRAY W/LINEN (Model PAIN0150C) due to calibration issues with sterilization and packaging equipment that could affect the sterility assurance level of the devices.

    Product
    Medline Convenience Kits: 1) BASIC NERVE BLOCK TRAY W/LINEN, Model Number: PAIN0150C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1404-2026·2026-02-25

    Medline Burn Care Kits Recalled Over Sterilization Calibration Issues

    Medline is recalling 291 units of three burn care convenience kits due to calibration issues with sterilization and packaging equipment that may affect sterility assurance.

    Product
    Medline Convenience Kits: 1) BURN PACK, Model Number: DYNJ15668R; 2) BURN PACK-LF, Model Number: DYNJ42829B; 3) BURN CARE PACK-LF, Model Number: DYNJT3437
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1352-2026·2026-02-25

    Olympus High Flow Insufflation Unit Recalled Due to Software Algorithm Issue

    Olympus Corporation of the Americas is recalling the Olympus High Flow Insufflation Unit (Model UHI) because a software algorithm issue may cause overpressure events.

    Product
    Olympus High Flow Insufflation Unit. Model Number: UHI. Used for insufflation of the abdominal cavity, and automatic suction and smoke evacuation to facilitate laparoscopic observation and treatment within the abdominal cavity.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1397-2026·2026-02-25

    Medline Sterile Surgical Kits Recalled Over Sterilization Equipment Calibration

    Medline is recalling 4,757 units of convenience surgical kits distributed worldwide due to calibration issues with sterilization and packaging equipment that may affect sterility assurance.

    Product
    Medline Convenience Kits: 1) PLASTIC BIN W/MISC KITS, Model Number: ACC010499; 2) KIT UROLOGY URETHROPLASTY, Model Number: DYKMBNDL117C; 3) KIT PLASTIC INSERT TISSUE EXPA, Model Number: DYKMBNDL158; 4) KIT PLASTIC ABDOMINOPLASTY, Model Number: DYKMBNDL170; 5) KIT PLASTIC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1414-2026·2026-02-25

    Medline Labor and Delivery Convenience Kits Recalled Over Sterilization Calibration

    Medline is recalling 27,320 labor and delivery convenience kits due to calibration issues with sterilization equipment that may affect the sterility assurance level of the devices.

    Product
    Medline Convenience Kits: 1) OB KIT, Model Number: DYKM2326; 2) KIT LABOR DELIVERY TUBAL LIGAT, Model Number: DYKMBNDL165; 3) KIT LABOR & DELIVERY D&C/D&E, Model Number: DYKMBNDL31; 4) KIT LABOR & DELIVERY CERCLAGE, Model Number: DYKMBNDL38; 5) L & D PACK-LF, Model Numbe
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1385-2026·2026-02-25

    Medline Tracheostomy Convenience Kits Recalled Over Sterilization Calibration Concerns

    Medline is recalling 753 units of its tracheostomy convenience kits and trach tote due to potential sterilization equipment calibration issues that may affect the sterility assurance level of the devices.

    Product
    Medline Convenience Kits: 1) KIT STC TRACHEOSTOMY, Model Number: DYKMBNDL55; 2) KIT STC TRACHEOSTOMY, Model Number: DYKMBNDL55A; 3) TRACH TOTE, Model Number: DYNJ85691
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1382-2026·2026-02-25

    Olympus Thunderbeat Surgical Device Recall Over Adverse Events

    Olympus is recalling 1,538 Thunderbeat 5 mm surgical devices worldwide due to continued reports of adverse events. The recall affects all units of Model No. TB-0510IC.

    Product
    Olympus Thunderbeat 5 mm, 10 cm, Inline Grip
    Category
    Medical Device
    Distribution
    Distributed nationwide