The Recall Desk

State

California product recalls

20,371 recalls have nationwide distribution and so reach California. 0 additional recalls listed California specifically in their distribution scope.

About recalls in California

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect California consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

15201–15225 of 20371

  • HighFDA (Devices)·Z-0169-2023·2022-11-09

    Cardiac Navigation Catheter Recalled for Cellulose Fiber Contamination

    Johnson & Johnson is recalling 91 THERMOCOOL SMARTTOUCH SF cardiac catheters nationwide due to manufacturing defects introducing cellulose fibers into the irrigation system. The contamination may prevent proper flushing, reduce cooling capability, or cause clotting complications.

    Product
    THERMOCOOL SMARTTOUCH SF Bi-Directional Navigation Catheter, REF: D-1348-05-S. Used for catheter-based cardiac electrophysiological mapping (stimulation and recording) and, in conjunction with an RF generator, for cardiac ablation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0161-2023·2022-11-09

    Surgical Cataract Packs with Compromised Breather Pouch Seals Recalled

    Medline recalls 708 Bausch + Lomb cataract surgical packs due to breather pouch seal defects that could compromise sterility of surgical instruments.

    Product
    BAUSCH + LOMB CATARACT PACK, REF VAL001CPMEA. Convenience kit used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0147-2023·2022-11-09

    Fogarty Biliary Balloon Probes recalled for latex deterioration

    Edwards Lifesciences is recalling Fogarty Biliary Balloon Probes due to confirmed latex deterioration in pouches. The recall affects 26,560 units distributed worldwide.

    Product
    Fogarty Biliary Balloon Probes Model Number: 410235FP 410405FP 410236FP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0157-2023·2022-11-09

    Bausch + Lomb Ophthalmic Surgical Kits Recalled for Sterile Packaging Defect

    Medline Industries is recalling 800 Bausch + Lomb Basic Ophthalmic surgical kits (Lot 22DBN365) for defective breather pouch seals. Opened seals in the packaging compromise the sterile conditions required for surgical procedures.

    Product
    BAUSCH + LOMB BASIC OPHTHALMIC PACK, REF LYN023BSBLB. Convenience kit used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0158-2023·2022-11-09

    Surgical Cataract Pack Recalled Due to Compromised Sterile Packaging

    Medline Industries is recalling 300 units of Bausch + Lomb Cataract Packs due to breather pouches with seal openings that may compromise sterility. The affected surgical kits were distributed nationwide.

    Product
    BAUSCH + LOMB CATARACT PACK, REF VAL009CTSGA. Convenience kit used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0156-2023·2022-11-09

    Surgical Kit Sterile Pouches with Seal Openings Recalled by Medline

    Medline is recalling approximately 160 surgical kits with defective breather pouches showing seal openings, potentially compromising sterility. The recall affects facilities in eight states nationwide.

    Product
    BAUSCH + LOMB PHACO PACK, REF LYN011PHNHD. Convenience kit used in surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V743000·2022-11-09

    2022 Nissan Pathfinder Seat Frame Welds May Fail in Crash

    Nissan is recalling certain 2022 Pathfinder vehicles because the second-row seat back frames may have insufficient welds that could separate. This could cause seats to fail to restrain occupants properly during a crash, increasing injury risk.

    Product
    NISSAN — 2022 NISSAN PATHFINDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0167-2023·2022-11-09

    NICU PICC Insertion Bundle Recalled for Breather Pouch Seal Defects

    Medline Industries recalls NICU PICC insertion bundles (50 kits) due to openings in breather pouch seals that compromise sterile barrier integrity. This Class II recall affects units distributed across the United States.

    Product
    CENTURION MEDICAL PRODUCTS NICU PICC INSERTION BUNDLE W/O, REF CVI4470. Convenience kit used in medical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0025-2023·2022-11-09

    Ranibizumab eye implant recalled for non-functioning delivery system

    Genentech is recalling Susvimo ocular implants (452 units nationwide) due to manufacturing defects in the drug delivery system. A few patients have experienced non-functioning implants.

    Product
    SUSVIMO — SUSVIMO (RANIBIZUMAB)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V618000·2022-11-08

    2023 Grand Design Momentum fifth wheels ramp door fall hazard

    Grand Design is recalling 2023 and 2022 Momentum fifth wheels due to a defective ramp door cut-off switch that may allow the electric ramp door to fall, creating an injury risk.

    Product
    GRAND DESIGN — 2023 GRAND DESIGN MOMENTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V652000·2022-11-08

    2021 Ford Explorer and Lincoln Aviator side air bag assembly defect

    Ford and Lincoln are recalling certain 2021 Explorer and Aviator vehicles. Side air bag attachment weld studs may detach during deployment, potentially failing to provide proper protection in a crash.

    Product
    FORD — 2021 FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V619000·2022-11-08

    2022 Chrysler Pacifica windshield wipers may not function due to loose arm nuts

    Certain 2022 Chrysler Pacifica and Voyager vehicles have improperly tightened windshield wiper arm nuts, causing malfunction. This reduces driver visibility and increases crash risk. Dealers will tighten the nuts free of charge.

    Product
    CHRYSLER — 2022 CHRYSLER PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V498000·2022-11-07

    BIG TEX 16GN trailers recalled for faulty spare tire mount

    Big Tex Trailer Manufacturing is recalling 2003-2022 16GN trailers with defective spare tire mounts that may detach, creating a road hazard.

    Product
    BIG TEX — 2010 BIG TEX 16GN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V471000·2022-11-06

    2020-2021 Nissan vehicles recalled for failed turn signal bulbs

    Nissan is recalling certain 2020-2021 Versa, Titan, and Titan XD vehicles because the front turn signal bulbs can crack and fail to illuminate, increasing the risk of crashes.

    Product
    NISSAN — 2021 NISSAN VERSA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V324000·2022-11-05

    2022 Hyundai IONIQ 5 Parking Brake Software Defect Recall

    Hyundai is recalling certain 2022 IONIQ 5 vehicles due to a software error in the Shifter Control Unit that may disengage the parking brake, allowing the vehicle to rollaway and increasing the risk of a crash.

    Product
    HYUNDAI — 2022 HYUNDAI IONIQ 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V322000·2022-11-05

    2022 KIA EV6 Parking Brake Software Defect May Cause Vehicle Rollaway

    Kia Motors America is recalling 2022 EV6 vehicles due to a software error in the Shifter Control Unit that may disengage the parking mechanism, allowing the vehicle to roll away unexpectedly.

    Product
    KIA — 2022 KIA EV6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V234000·2022-11-04

    Newmar RVs recalled for unsecured seat wiring fire risk

    Newmar is recalling multiple 2019–2022 RV models due to unsecured wiring beneath seats that can cause electrical short circuits and fire. Owners should contact their dealer for free inspection and repair.

    Product
    NEWMAR — 2019 NEWMAR BAY STAR SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V143000·2022-11-03

    Forest River 2022 Travel Trailers Recalled for Coupler Weld Defect

    Forest River is recalling certain 2022 travel trailers due to improperly welded couplers that may cause trailer separation from the tow vehicle. Dealers will replace the coupler at no charge.

    Product
    FOREST RIVER — 2022 FOREST RIVER XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23034·2022-11-03

    BLACK+DECKER Garment Steamers Recalled for Burn Hazard from Hot Water

    Empower Brands recalls about 518,500 BLACK+DECKER Model HGS011 Easy Garment Steamers because they can expel, spray, or leak hot water during use, posing a burn hazard. The company has received 241 reports of hot water expelling, including 32 reports of burn injuries.

    Product
    BLACK+DECKER Model HGS011 Easy Garment Steamers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23031·2022-11-03

    Bolt Foldable Children's Scooters Recalled for Excessive Lead Paint

    Anker Play Products is recalling about 5,000 Bolt Foldable Children's Scooters sold at discount stores from March through May 2022. The paint contains lead levels exceeding the federal ban, creating a lead poisoning hazard for young children.

    Product
    Bolt Foldable Children's Scooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23708·2022-11-03

    Myx Connected Exercise Bicycles Recalled for Pedal Detachment Risk

    Myx is recalling approximately 162,000 MYX I, MYX II, and MYX II Plus exercise bicycles because pedals can loosen or detach during use, causing injury. Myx has received 864 reports of pedal loosening or detachment, including 75 injury reports involving bruises and cuts.

    Product
    MYX I, MYX II and MYX II Plus Connected Exercise Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V149000·2022-11-03

    2022 Ford Escape High Voltage Battery Failure Causes Drive Power Loss

    The high voltage battery in 2021-2022 Ford Escape and 2022 Lincoln Corsair hybrid vehicles may fail, causing sudden loss of drive power and increasing crash risk.

    Product
    FORD — 2022 FORD ESCAPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V144000·2022-11-03

    Keystone Travel Trailers Recalled for Faulty Wiring Disabling Safety Alarms

    Keystone is recalling 2021-2022 Sprinter and Bullet models plus multiple 2022 travel trailer and fifth-wheel variants due to faulty solar controller wiring that can disable carbon monoxide and propane gas detectors.

    Product
    KEYSTONE — 2022 KEYSTONE SPRINTER
    Category
    Vehicle
    Distribution
    Distributed nationwide