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.

14051–14075 of 20364

  • HighNHTSA·23V049000·2023-03-02

    Winnebago motorhome cooktops recalled for potential gas leak and fire risk

    Winnebago is recalling certain Travato, Solis, and Ekko motorhomes with Suburban cooktops that may develop gas leaks due to fractured burner tubes. In the presence of an ignition source, a leak poses a fire risk.

    Product
    WINNEBAGO — 2022 WINNEBAGO TRAVATO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V051000·2023-03-02

    BMW S 1000 XR and R motorcycles recall for deactivated safety feature

    BMW is recalling 2020-2023 S 1000XR and 2022-2023 S 1000R motorcycles because a software update may have deactivated the front wheel lift-off assistant feature without notifying riders, increasing the risk of unexpected handling and loss of control.

    Product
    BMW — 2021 BMW S 1000 XR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23137·2023-03-02

    TJX Office Chairs Recalled Due to Fall Hazard

    The TJX Companies is recalling approximately 81,700 office chairs because the back can break or detach from the seat base when occupied, posing a fall hazard. The firm has received 12 reports of the chair back failing, including 10 reports of injuries.

    Product
    Office Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23141·2023-03-02

    Helly Hansen Adult Workwear Sweatshirts and Hoodies Recalled for Burn Hazard

    Helly Hansen is recalling about 13,900 adult workwear sweatshirts and hoodies because they fail to meet federal flammability standards for clothing textiles, posing a risk of burn injuries.

    Product
    Adult workwear sweatshirts and hoodies
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23731·2023-03-02

    Classic Whimsy Children's Pajamas Recalled for Flammability Standard Violation

    Smocked Runway is recalling about 7,200 Classic Whimsy children's pajamas that fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries. Consumers should stop using the product immediately and contact the manufacturer for return instructions.

    Product
    Classic Whimsy children's pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23730·2023-03-02

    Multi-Purpose Kids Bike Helmets Recalled for Head Injury Risk

    Ouwoer Kids Bike Helmets sold on Amazon from March to November 2022 fail to meet federal safety standards and may not protect children in a crash. About 120 units are affected; no injuries have been reported.

    Product
    Multi-Purpose Kids Bike Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23138·2023-03-02

    Patagonia Infant Capilene Base Layer Sets Recalled for Choking Hazard

    Patagonia is recalling about 8,000 Infant Capilene Midweight Base Layer Sets because snaps on the bodysuit can detach, posing a choking hazard to infants. One incident of a snap detaching and being mouthed by a baby has been reported.

    Product
    Infant Capilene Midweight Base Layer Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23140·2023-03-02

    RELiON InSight Series Lithium Batteries Recalled for Thermal Burn and Fire Risk

    RELiON Battery is recalling certain lots of InSight Series 48V lithium-ion batteries because they can overheat, posing thermal burn and fire hazards. The company has received five reports of overheating with no injuries reported to date.

    Product
    RELiON InSight Series® lithium batteries
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23139·2023-03-02

    Primark Children's Bamboo Plates Recalled for Lead and Formaldehyde

    Primark is recalling about 1,665 children's bamboo plates sold from October 2021 through August 2022 because they contain elevated levels of lead and formaldehyde, which are toxic if ingested by children.

    Product
    Children's Bamboo Plates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23732·2023-03-02

    DR Power PRO XL501 Chipper Shredders Recalled for Laceration Hazard

    DR Power is recalling about 2,100 PRO XL501 Chipper Shredders because the fin scroll can fail and eject metal pieces from the hopper during operation. No injuries have been reported, but the company has received six reports of metal ejection.

    Product
    DR®Power PRO XL501 Chipper Shredders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23733·2023-03-02

    CTRL Imperial Wakeboard Bindings Recalled Due to Fall Hazard

    Active Sports is recalling CTRL Imperial Wakeboard Bindings because the binding can partially detach from the baseplate or the external mount can crack, causing users to lose balance and fall into the water. The company has received 21 reports of detachment or cracking but no injuries have been reported.

    Product
    CTRL Imperial Wakeboard Bindings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1138-2023·2023-03-01

    FDA Recalls NovaStar TS Standard Elbow Reusable Components for Magnet Interference Risk

    Draeger Medical is recalling 893 units of NovaStar TS Standard elbow components due to magnets that could interfere with medical devices and metallic implants.

    Product
    NovaStar TS, Standard elbow, Reusable, Material Numbers MP01579 (Size S), MP01580 (Size M), and MP01581 (Size L)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V026000·2023-03-01

    Volkswagen Atlas and Cross Sport steering knuckle fracture recall

    Front steering knuckles in certain Volkswagen Atlas and Atlas Cross Sport vehicles may fracture, causing loss of vehicle control and increasing crash risk. Volkswagen will inspect and replace affected knuckles free of charge.

    Product
    VOLKSWAGEN — 2021 VOLKSWAGEN ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1137-2023·2023-03-01

    NovaStar TS Anti-Asphyxia Valve recalled for magnetic interference risk

    Draeger Medical recalls NovaStar TS Anti-Asphyxia Valves due to magnets that may interfere with implanted and non-implanted medical devices and metallic implants.

    Product
    NovaStar TS, Anti-Asphyxia Valve, Reusable, Material Numbers MP01576 (Size S), MP01577 (Size M), and MP01578 (Size L)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1144-2023·2023-03-01

    Hologic Mammography Systems Recalled for Unexpected C-Arm Movement

    Hologic is recalling 797 units of its 3Dimensions/Selenia Dimensions mammography systems nationwide due to unexpected C-arm movement that may cause blunt trauma.

    Product
    Hologic 3Dimensions/Selenia Dimensions Models: RM-SDM-00001-3D SDM-00001-2D SDM-00001-3D SDM-05000-3D3 SDM-05000-2DC SDM-00001-M3D SDM-05000-3DC SDM-SYS-6000-3D SDM-05000-2D3 SDA-SYS-3000-2D SDM-00001 SDM-SYS-9000-2D SDM-00001-M2D 3DM-SYS-STD 3DM-SYS-STD-NS SDM-
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0336-2023·2023-03-01

    Levothyroxine Oral Solution TIROSINT Recalled Due to Subpotency

    IBSA PHARMA is recalling TIROSINT (levothyroxine sodium) oral solution due to subpotency in specific batches. The affected product may contain less active ingredient than labeled.

    Product
    TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1162-2023·2023-03-01

    Medline Sterile Maximum Barrier Pack-LF units recalled for sterilization failure

    Medline Industries recalls approximately 720 Sterile Maximum Barrier Pack-LF units due to improper component placement preventing sterilization. The affected packs were distributed in Arkansas, Colorado, and Georgia.

    Product
    (1) Medline Sterile Maximum Barrier Pack-LF, Item DYNJ0248546C, 6 kits per case, contains BD Chloraprep Hi-Lite Orange, 10.5 mL Applicator, Vendor PN: 930715NS; (2) Medline Sterile Maximum Barrier Pack-LF, Item DYNJ0248546D, 6 kits per case, contains BD Chloraprep Hi-Lite Oran
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0347-2023·2023-03-01

    Sodium Chloride Injection Recalled for Incomplete Seal and Potential Leakage

    B. Braun Medical is recalling 0.9% Sodium Chloride Injection due to possible incomplete container seals that may leak. The recall involves 483,229 bags distributed nationwide.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0337-2023·2023-03-01

    TIROSINT Levothyroxine Sodium Oral Solution Recalled for Subpotency

    TIROSINT (levothyroxine sodium) oral solution has been recalled nationwide by IBSA Pharma Inc. due to subpotency, with the affected medication containing less active ingredient than labeled.

    Product
    TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0341-2023·2023-03-01

    Thyroid Drug TIROSINT Recalled Due to Subpotent Formulation

    IBSA Pharma Inc. recalls TIROSINT (levothyroxine sodium) oral solution nationwide due to subpotent formulation containing less active ingredient than labeled.

    Product
    TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1154-2023·2023-03-01

    Folate test kits recalled for calibration error causing inaccurate results

    Siemens is recalling ADVIA Centaur Folate 500 test kits because a calibration error causes inaccurate, falsely low results when testing serum samples, potentially affecting diagnostic accuracy.

    Product
    ADVIA Centaur Folate 500 test kit (REF)-For in vitro diagnostic use in the quantitative determination of folate in human serum and red blood cells. Siemens Material Number (SMN): 10331250 Siemens Material Number (SMN): 10325366
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1164-2023·2023-03-01

    Luminos Agile Diagnostic Imaging System Collision Risk Recall

    Siemens recalls Luminos Agile imaging systems that may collide with ceilings or walls due to default configuration settings, potentially causing serious injury to staff or patients.

    Product
    Luminos Agile with software VC10 - A diagnostic imaging system for radiographic and fluoroscopic studies. Model Number: 10502200
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1161-2023·2023-03-01

    Sterile Oncology Port Access Tray Recalled for Sterilization Failure

    Medline is recalling sterile oncology port access trays in which some components were not properly sterilized due to improper placement during manufacturing. Healthcare facilities should immediately discontinue use of affected units.

    Product
    Medline Sterile Oncology Port Access Tray, Item #DYNDC2239, 20 sterile kits per case, containing Ethicon Biopatch Protective Disk with CHG, Disk with Chlorhexidine Gluconate (CHG), DRSG Biopatch 1IN NS, VPN: 10150;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1143-2023·2023-03-01

    Hepatitis B Diagnostic Test Kits Recalled for Test Interference

    Siemens is recalling ADVIA Centaur diagnostic test kits used to detect hepatitis B antibodies due to test interference that can produce false positive results when performed before another hepatitis B test on the same sample.

    Product
    ADVIA Centaur XP and ADVIA Centaur XPT Anti-HBe2 (aHBe2) 50T- In vitro diagnostic immunoassay for the qualitative detection of antibodies to the e antigen of the hepatitis B virus (HBV) in human pediatric (2-21 years old) and adult serum, EDTA plasma, or lithium heparin. Siemens
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0338-2023·2023-03-01

    Thyroid Medication TIROSINT Levothyroxine Sodium Nationwide Recall for Subpotency

    IBSA Pharma Inc. is recalling TIROSINT (levothyroxine sodium) oral solution nationwide due to subpotency. Two lot numbers are affected: Lot #220407 (Exp. 10/2023) and Lot #220960 (Exp. 03/2024).

    Product
    TIROSINT — TIROSINT (LEVOTHYROXINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide