The Recall Desk

State

California product recalls

20,199 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.

9326–9350 of 20199

  • HighCPSC·24221·2024-05-02

    Dixon Ticonderoga Recalls Creativity Street Foam Pattern Rollers for Excess Lead

    Dixon Ticonderoga is recalling Creativity Street Foam Pattern Rollers because the handles contain lead levels above the federal limit. Lead is toxic if ingested by young children and can cause adverse health effects.

    Product
    Creativity Street Foam Pattern Rollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V097000·2024-05-02

    Vehicle recall: Mercedes-Benz G550 and AMG G63 front axle wiring chafe

    2019–2021 Mercedes-Benz G550 and AMG G63 models may lose anti-lock brakes and stability control due to front axle wiring harness chafing against the oil cooler, increasing crash risk.

    Product
    MERCEDES-BENZ — 2019 MERCEDES-BENZ G550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24223·2024-05-02

    Arctic Cat Snowmobiles Recalled Due to Clutch Laceration Hazard

    Arctic Cat is recalling approximately 16,200 model year 2017–2021 and certain 2022 snowmobiles from the 8000 and 9000 series because the drive clutch can break and allow fragments to escape the shielding, causing laceration injuries.

    Product
    Arctic Cat 8000 and 9000 Series Snowmobiles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V099000·2024-05-02

    2023 BMW vehicles recalled for unintended power window and sunroof closure

    BMW is recalling 2023 and some 2022 model-year vehicles for a software defect allowing power windows and sunroofs to close without the digital key present, posing a risk of injury to occupants.

    Product
    BMW — 2023 BMW ALPINA B8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24218·2024-05-02

    Polaris Model Year 2024 Prostar S4 Titan Adventure Snowmobiles Recalled for Fire Hazard

    Polaris is recalling about 240 Model Year 2024 Prostar S4 Titan Adventure 155 ES Snowmobiles because the fuel pump flange assembly can leak fuel, creating a fire hazard and risk of serious injury. No injuries have been reported.

    Product
    Model Year 2024 Prostar S4 Titan Adventure 155 ES Snowmobiles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24224·2024-05-02

    Bausch + Lomb recalls Project Watson dog eyelid wipes for bacteria risk

    Bausch + Lomb is recalling about 32,000 units of Project Watson Eyelid Wipes for Dogs due to risk of bacterial and fungal growth in the container after opening, which could cause serious infection in immunocompromised people or those with wounds.

    Product
    Project Watson Eyelid Wipes for Dogs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24216·2024-05-02

    SKIMS Children's Pajama Sets Recalled for Burn Hazard

    SKIMS is recalling about 1,200 children's fleece pajama sets that fail to meet federal flammability regulations for children's sleepwear, posing a risk of burn injuries. Consumers should stop using them immediately and contact SKIMS for a refund.

    Product
    SKIMS Children's Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V101000·2024-05-02

    2022 Mercedes-Benz Sprinter Airbag Non-Deployment Risk from Wiring Defect

    Certain 2022 Mercedes-Benz Sprinter vehicles with adjustable front swivel-seats have wiring harnesses that may be incorrectly installed, causing side airbags to fail deployment in a crash and increasing injury risk.

    Product
    MERCEDES-BENZ — 2022 MERCEDES-BENZ SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24215·2024-05-02

    Igloo Youth Sipper Bottles Recalled Due to Choking Hazard

    Igloo Products is recalling about 31,500 Youth Sipper Bottles because the silicone cover on the sipper can detach while in use, posing a choking hazard to children. One incident was reported, but no injuries have occurred.

    Product
    Youth Sipper Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24217·2024-05-02

    Mill Valley Jr. Youth Dressers Recalled for Tip-Over and Entrapment Hazards

    LFN Limited is recalling about 200 Mill Valley Jr. six-drawer youth dressers sold at Rooms To Go from December 2023 through January 2024 due to tip-over and entrapment hazards if not anchored to the wall. No injuries have been reported.

    Product
    Mill Valley Jr. six-drawer youth dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24220·2024-05-02

    Honda Lawnmowers and Engines Recalled for Dangerous Starter Rope Hazard

    American Honda Motor is recalling lawnmowers and replacement engines with faulty camshafts that can cause the starter rope to suddenly retract, injuring users. About 200 additional replacement engines are included in this expansion of a previous recall.

    Product
    Honda Lawnmowers, Replacement Engines, and Pressure Washers Engines
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24222·2024-05-02

    DR Power Equipment Leaf Blowers and Vacuums Recalled for Laceration Hazard

    DR Power Equipment is recalling about 57,200 walk-behind and tow-behind leaf blowers and vacuums because internal pieces can come loose and be ejected, posing a laceration risk to users and bystanders. No injuries have been reported.

    Product
    Walk-Behind Leaf Blowers and Vacuums, and Tow-Behind Leaf Vacuums
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0459-2024·2024-05-01

    FDA Recalls Alcoholada Gel Pain Reliever Over Methanol Contamination

    Alcoholada Gel pain reliever is being recalled because the ethanol ingredient contains methanol contamination. The FDA classified this as a Class I recall affecting 9,625 bottles distributed nationwide.

    Product
    Alcoholada Gel, Pain Relieving Gel, 0.5% Lidocaine Hydrochloride, packaged in (a) 8.5 fl oz (251 mL) plastic bottle UPC 0 82252 03120 9 (b) 2.2 fl oz (65 mL) plastic bottle, UPC 0 82252 34030 1 , Manufactured in Aruba by Aruba Aloe Balm Inc., Pitastraat 115, Aruba, Dutch Caribbe
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0453-2024·2024-05-01

    Male Sexual Enhancement Product Recalled for Undeclared Pharmaceutical Ingredients

    Pyramids Wholesale Inc. is recalling all lots of GoHARD 25000 because it contains undeclared sildenafil and tadalafil. The product was marketed without FDA approval for these prescription-strength drugs.

    Product
    GoHARD 25000, Male Sexual Enhancement, Honey, 100% Natural, UPC: N/A.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0450-2024·2024-05-01

    FDA Recalls Flower Power Female Enhancement for Undeclared Sildenafil and Tadalafil

    Flower Power CBD infused Female Enhancement contains undeclared sildenafil and tadalafil. These prescription drugs were not disclosed to consumers and the product was marketed without FDA approval.

    Product
    Flower Power, CBD infused Female Enhancement, 59 ml bottle, UPC 0 678741 351646.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0452-2024·2024-05-01

    Pink Pussycat Honey recalled for undeclared sildenafil and tadalafil content

    Pyramids Wholesale Inc. is recalling Pink Pussycat Honey because it contains undeclared sildenafil and tadalafil and was marketed without FDA approval. The recall affects all lots nationwide.

    Product
    Pink Pussycat Honey, net wt: 20gx12 sachets, UPC 7 918750 046557
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0470-2024·2024-05-01

    ForeverMen Natural Energy Boost Capsules Recalled for Undeclared Sildenafil

    ForeverMen Natural Energy Boost Capsules contain undeclared sildenafil and are marketed without FDA approval, making them an unapproved drug. Consumers should stop using the product immediately.

    Product
    ForeverMen Natural Energy Boost Capsules, packaged in a box containing a 10-count blister card.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0451-2024·2024-05-01

    Samurai-X Honey 6800 Recalled for Undeclared Drug Ingredients

    Samurai-X Honey 6800, manufactured by Pyramids Wholesale Inc., is recalled for containing undeclared sildenafil and/or tadalafil. The product was distributed nationwide and marketed without FDA drug approval.

    Product
    Samurai-X Honey 6800, UPC 2 56891 27553 3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0448-2024·2024-05-01

    Spanish Fly 22K Capsules Recalled for Undeclared Prescription Drug Ingredients

    Spanish Fly 22K capsules contain undeclared sildenafil and/or tadalafil and were marketed without FDA approval. The product poses serious health risks from these unapproved pharmaceutical ingredients.

    Product
    Spanish Fly 22K capsules, 2-count box, UPC 0 664979 979455
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0449-2024·2024-05-01

    Honey product recalled nationwide for undeclared sildenafil and tadalafil

    Pyramids Wholesale Inc. is recalling Weiner Boner Honey due to undeclared sildenafil and tadalafil. The product was distributed nationwide without FDA approval.

    Product
    Weiner Boner Honey, 12g packet, 100% Organic Formula.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0458-2024·2024-05-01

    Sexual Enhancement Product Recalled for Undeclared Prescription Drugs

    Pyramids Wholesale Inc. is recalling HONEY MANUKA BUNNY LOVE nationwide because it contains undeclared sildenafil and/or tadalafil—prescription medications—and was marketed without FDA approval.

    Product
    HONEY MANUKA BUNNY LOVE, 12g, All Natural Sexual Enhancement, UPC: N/A
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0457-2024·2024-05-01

    Male Performance Enhancer Recalled for Undeclared Sildenafil and Tadalafil

    ALPHASTRIP Male Performance Enhancer strips are being recalled nationwide because they contain undeclared sildenafil and tadalafil. The product was marketed without FDA approval.

    Product
    ALPHASTRIP MALE PERFORMANCE ENHANCER, The fastest acting sublingual, Serving Size (1 strip), Distributed by: GALT INT'L
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0454-2024·2024-05-01

    FDA Recalls libigrow RED DRAGON+ Capsules for Undeclared Sildenafil and Tadalafil

    Pyramids Wholesale Inc. is recalling libigrow RED DRAGON+ capsules nationwide because they contain undeclared sildenafil and tadalafil, prescription medications not approved by the FDA for this product.

    Product
    libigrow RED DRAGON+, Maximum Strength Formula, 2 capsules per box, UPC 7 05105 83073 5.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0460-2024·2024-05-01

    FDA Recalls Aruba Aloe Hand Sanitizer for Methanol Contamination

    FDA is recalling 5,299 bottles of Aruba Aloe Hand Sanitizer Gel nationwide due to methanol contamination in the ethanol ingredient. Consumers should stop using the product immediately.

    Product
    Aruba Aloe Hand Sanitizer Gel, 80% Alcohol, 12 fl oz (355 mL) plastic bottle, Manufactured in Aruba by Aruba Aloe Balm Inc., Pitastraat 115, Aruba, Dutch Caribbean. UPC 0 82252 03300 5
    Category
    Drug
    Distribution
    Distributed nationwide