The Recall Desk

State

California product recalls

20,364 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.

14551–14575 of 20364

  • HighCPSC·23097·2023-01-19

    Children's Pajama Sets Recalled for Flammability Standards Violation

    Selfie Craft Company children's pajama sets fail to meet federal flammability standards for sleepwear, posing a burn injury risk. About 38,740 units sold online and in boutiques from November 2017 through June 2022 are affected.

    Product
    Children's Pajama Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23095·2023-01-19

    Vaenait Baby Children's Robes Recalled for Flammability Hazard

    Vaenait Baby children's robes fail federal flammability standards for sleepwear, posing a burn injury risk. About 2,400 robes sold nationwide between December 2019 and June 2022 are affected.

    Product
    Children's robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23103·2023-01-19

    NewCosplay Children's Sleepwear Recalled for Flammability Standards Violation

    NewCosplay long-sleeved children's sleepwear fails to meet federal flammability standards and poses a burn hazard. The recalled garments were sold exclusively on Amazon from October 2021 through May 2022.

    Product
    Children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23104·2023-01-19

    NewCosplay Children's Sleepwear Recalled for Flammability Standards Violation

    About 2,140 units of NewCosplay children's sleepwear fail to meet federal flammability standards and pose a burn injury risk. The recalled garments were sold on Amazon from October 2021 through May 2022.

    Product
    Children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23101·2023-01-19

    NewCosplay Children's Sleepwear Recalled for Flammability Standards Violation

    Hainan Chong Yu Industrial's NewCosplay children's sleepwear fails federal flammability standards and poses a burn injury risk. About 2,360 units sold on Amazon from October 2021 through May 2022 are affected.

    Product
    Children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23093·2023-01-19

    Vanessa 42-inch Fire Tables Recalled for Fire Hazard

    Ove Decors' Vanessa 42-inch fire tables are recalled because the gas hose can melt when contacting the heat shield, causing the table to catch fire. About 470 units sold online from April 2020 through October 2022.

    Product
    Vanessa 42-inch Fire Tables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23094·2023-01-19

    Taylor and Finch Six-Wick Scented Candles Recalled for Fire and Injury Hazards

    Ross Stores is recalling about 5,800 Taylor and Finch six-wick scented candles because they can combust while lit, causing the glass container to break and posing fire and injury hazards. Ross has received five reports of combustion, including one report of minor injury.

    Product
    Taylor and Finch six-wick scented candles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23105·2023-01-19

    Meguiar's Heavy Duty Headlight Sealant recalled for non-compliant packaging

    Meguiar's is recalling about 140,000 units of Heavy Duty Headlight Sealant because the packaging does not meet federal child-resistant requirements. Young children could be poisoned if they swallow the contents.

    Product
    Heavy Duty Headlight Sealant
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23098·2023-01-19

    Sakar International Recalls Three Helmet Models Due to Head Injury Risk

    Sakar International is recalling about 33,100 Credhedz Lizard, Crayola Dry-Erase, and Tony Hawk multi-purpose helmets because they do not meet federal safety standards for positional stability and retention, posing a risk of head injury in a crash.

    Product
    Credhedz Lizard Helmets, Crayola Dry Erase Helmets and Tony Hawk Multi-Purpose Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23096·2023-01-19

    Lifetime Brands Recalls Hot Chocolate Pots Due to Fire Hazard

    Lifetime Brands has recalled about 2,700 hot chocolate pots sold at Williams-Sonoma because they are mislabeled as microwave safe. If microwaved, the metallic paint can spark and cause a fire.

    Product
    Hot Chocolate Pots
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23099·2023-01-19

    NewCosplay Children's Sleepwear Recalled for Flammability Violation

    NewCosplay branded children's sleepwear fails to meet federal flammability standards, posing a burn risk. About 780 units sold on Amazon from November 2021 through May 2022 are subject to recall.

    Product
    Children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23100·2023-01-19

    NewCosplay Children's Sleepwear Recalled for Flammability Violation

    Weihai Juanhai Decoration Material's NewCosplay children's sleepwear fails to meet federal flammability standards, posing a burn risk. About 280 units were sold on Amazon between December 2021 and May 2022.

    Product
    Children's sleepwear
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0877-2023·2023-01-18

    Mahurkar Dialysis Catheters Recalled Due to Leaking Hub Defect

    Covidien LP is recalling Mahurkar dialysis catheters for a potential leaking condition in the hub that may cause unanticipated fluid return during use. Over 359,000 units are affected worldwide.

    Product
    MAHURKAR 13.5Fr High Flow Dual Lumen Acute Dialysis Catheter, Sterile, Single Use, Rx Only: 13.5cm, Straight Extensions, Kit - Model No. 8888135131; 13.5 cm, Curved Extensions, Kit - Model No. 8888135132; 13.5cm, Pre-Curved, Kit - Model No. 8888135133; 13.5cm, Straight
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0884-2023·2023-01-18

    Philips Garbin Ventilator Foam May Separate, Blocking Air Intake

    Silicone foam in some Philips Garbin Ventilators may separate and block the air inlet, reducing therapy volume and causing alarms. Nine units are affected.

    Product
    Philips Garbin Ventilator, Model Number 1058180B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0908-2023·2023-01-18

    Philips Fetal Spiral Electrode may break off during labor monitoring

    Philips is recalling fetal spiral electrodes used for labor monitoring because the spiral tip can break off during use, requiring surgery to remove the fragment from the newborn.

    Product
    Philips Fetal Spiral Electrode-intended for patients requiring fetal heart rate monitoring during labor. PN: 989803137631
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0883-2023·2023-01-18

    Philips Trilogy 100 and 200 Ventilators Recalled for Foam Separation Risk

    Silicone foam in some Philips Trilogy 100 and 200 ventilators may separate and block the air inlet, potentially reducing therapy delivery. This is an FDA Class I recall.

    Product
    Philips Trilogy 200 Ventilator, Model Numbers 1040005, U1040005, 1040005B, U1040005B, CA1032800B, CA1032800, KO1032800, 1032800, R1032804TP, R1032804B, R1032804TPV, 1032804B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0882-2023·2023-01-18

    Philips Trilogy 100 Ventilator Foam May Separate and Block Air Inlet

    Silicone sound abatement foam in some Philips Trilogy 100 ventilators may separate and block the air inlet, potentially reducing delivered therapy volume or pressure and causing device alarms.

    Product
    Philips Trilogy 100 Ventilator, Model Numbers 1054260, 1054096, U1054260, U1054260B, 1054260B, CA1054096B, BT1054260, 1054096B, R1054260, RSL1054260, CA1054096, R1054260B, R1054655TPV, AU1054096, AU1054096B, 1054096B, 1054097, BR1054096, LA1054096, CN1054096, KO1054096, KR1054096
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0112-2023·2023-01-18

    Prostaglandin E1 Injection Vials Recalled for Sterility Issues

    Northern VA Compounders PLLC is recalling Prostaglandin E1 Injection Solution vials nationwide due to lack of assurance of sterility. Patients should contact their healthcare provider.

    Product
    Prostaglandin (E1) Injection Solution, 40mcg/ml, 2.5 mL Multiple-Dose vials, Rx Only, Compounded by: Akina Pharmacy, 23475 Rock Haven Way Suite 105, Sterling, VA 20166.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0953-2023·2023-01-18

    Medtronic RadiaLux Lighted Retractor recalled for defective sterile pouch seal

    Medtronic is recalling 2,317 RadiaLux Lighted Retractor units due to defects in the sterile pouch seal that increase contamination risk and potential post-operative infection.

    Product
    RadiaLux Lighted Retractor (Pink), REF: 50-101-1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0122-2023·2023-01-18

    BiMix Injection Recalled for Lack of Assurance of Sterility

    Northern VA Compounders has recalled BiMix Injection due to lack of assurance of sterility. Patients using affected lots should consult their healthcare provider.

    Product
    BiMix Injection (Papaverine HCl/Phentolamine Mesylate) 30mg/0.5mg/mL INJECTABLE, packaged in 2.5 mL Multiple-Dose vials, Rx Only, Compounded by: Akina Pharmacy, 23475 Rock Haven Way Suite 105, Sterling, VA 20166.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0930-2023·2023-01-18

    Medline CISION Sterile Surgical Blades Recalled for Sterile Packaging Breach Risk

    Medline Industries is recalling CISION Sterile Blades used in surgical procedures due to potential for the blade to puncture the sterile outer packaging, breaching sterility. No injuries reported.

    Product
    Medline CISION Sterile Blades. Labeled as follows with corresponding Item Number. a. STERILE BLADE NO. 10 CARBON STEEL, Item Number: CISION10CS; b. STERILE BLADE NO. 10 CARBON STEEL RIB, Item Number: CISION10CSR; c. STERILE BLADE NO. 11 CARBON STEEL, Item Number: CISION11
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0253-2023·2023-01-18

    Sanders Dark Chocolate Maple Sea Salt Caramel Recalled for Foreign Material

    Sanders Candy LLC is recalling Sanders Dark Chocolate Maple Sea Salt Caramel due to brush bristles found in the product. Consumers should not consume affected units.

    Product
    Sanders Dark Chocolate Maple Sea Salt Caramel: No UPC 6oz. foil bag
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0954-2023·2023-01-18

    Orthopedic Implant Cage Recalled for Incorrect Internal Material

    Specific lots of CoreLink FLXFIT 15 orthopedic implant cages contain stainless steel internal components instead of the specified titanium alloy. The 18 affected units were distributed nationwide.

    Product
    CoreLink LLC, FLXFIT 15, 32MM X 8MM, CAGE, REF: AT3208
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0251-2023·2023-01-18

    Sanders Milk Chocolate Sea Salt Pecan Cluster Recalled for Brush Bristles

    Sanders Candy LLC recalls Sanders Milk Chocolate Sea Salt Pecan Cluster due to foreign material—pieces of cleaning brush bristles—found in the product. The recall affects nearly 1 million units distributed nationwide and in Canada.

    Product
    Sanders Milk Chocolate Sea Salt Pecan Cluster: 0-35900-25550-2 .5OZ Individual Wrapped 0-35900-27486-2 25OZ Tub 0-35900-30971-7 18OZ Tub 0-35900-30170-4 7OZ Pouch
    Category
    Food
    Distribution
    Distributed nationwide