The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Filters

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

2551–2575 of 36527

  • SevereFDA (Devices)·Z-1727-2025·2025-05-21

    iGo2 DC Car Adapter Recall: Overheating and Housing Deformation Risk

    Medical Depot Inc. is recalling 89,532 units of the iGo2 DC Car Adapter used with iGo2 Portable Oxygen Concentrator Systems. The DC power supply housing may become excessively hot to the touch and deform, posing a burn and fire hazard.

    Product
    iGo¿2 DC Car Adapter to be used with iGo¿2 Portable Oxygen Concentrator Systems. Power cord allows the user to operate the device in a vehicle.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1725-2025·2025-05-21

    Welch Allyn Life2000 Ventilation System Recalled for Cybersecurity Vulnerability

    Baxter Healthcare Corporation is recalling the Welch Allyn Life2000 Ventilation system due to a cybersecurity vulnerability discovered through internal testing. The recall affects 4,881 units distributed worldwide.

    Product
    Welch Allyn Life2000 Ventilation system, Product Codes: 1) BT-20-0002; 2) BT-20-0002A; 3) BT-20-0002AP; 4) BT200007; 5) BT-20-0007; 6) BT200011; 7) BT-20-0011; 8) RMS010118CP.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1698-2025·2025-05-21

    AirLife Infant Heated Wire Circuit Adapter Disconnection Risk Recall

    Vyaire Medical is recalling the AirLife Infant Heated Wire Circuit (model AH265) because adapters may disconnect during setup or use, potentially interrupting ventilation to newborns. Disconnection can cause hypoxia, hypercapnia, and organ failure.

    Product
    Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit Model/Catalog Number: AH265 Software Version: N/A Product Description: AirLife Infant Heated Wire Circuit Kit Dual-limb, Dual-heat, high-flow circuit (>4 L/min) Contains AH165 Circuit, AH290 Chamber Compone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1730-2025·2025-05-21

    MedicaLyte Liquid Bicarbonate Concentrate Recalled for Foreign Matter

    Nipro Renal Solutions USA is recalling MedicaLyte Liquid Bicarbonate Concentrate (models BC+201 and BC+100) due to the potential presence of visible foreign matter in the product.

    Product
    MedicaLyte Liquid Bicarbonate Concentrate. Model Numbers: BC+201 (45X), BC+100 36.83X. Plastic bottle packaged in corrugated shipper cases (4 bottles per shipper case).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1697-2025·2025-05-21

    AirLife Infant Heated Wire Circuit Adapter Disconnection Risk

    Vyaire Medical is recalling the AirLife Infant Heated Wire Circuit (Model AH165) because adapters may disconnect during setup or use, interrupting ventilation to infants and potentially causing severe complications.

    Product
    Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit Model/Catalog Number: AH165 Software Version: N/A Product Description: AirLife Infant Heated Wire Circuit dual-limb, dual-heat, high-flow circuit (>4 L/min) Component: No. a conduit for respiratory gas bet
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1763-2025·2025-05-21

    LifeShield Infusion Safety Software Recalled for Drug Library Defects

    ICU Medical is recalling LifeShield Drug Library Management software v2.1 and v2.2 due to defects that could allow over-delivery of medication to patients or unauthorized modification of drug parameters.

    Product
    LifeShield Drug Library Management (DLM), LifeShield Infusion Safety Software SUite v2.1 and v2.2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·017-2025·2025-05-20

    Snack Mania Recalls Uninspected Frozen Chicken Coxinhas Products

    Snack Mania Brazilian Delights Corp. is recalling approximately 9,722 pounds of frozen chicken coxinhas produced without federal inspection. No illnesses have been reported.

    Product
    Snack Mania Brazilian Delights Corp., Recalls Ready-To-Eat Chicken Coxinhas Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereUSDA FSIS·016-2025·2025-05-20

    Bourgeois Smokehouse Recalls Smoked Andouille Sausage Due to Listeria

    Bourgeois Smokehouse is recalling approximately 100 pounds of ready-to-eat smoked andouille sausage sold in Alabama, Louisiana, and Mississippi due to possible Listeria monocytogenes contamination.

    Product
    Bourgeois Smokehouse Recalls Ready-To-Eat Smoked Andouille Sausage Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·25V319000·2025-05-16

    Isuzu Recalls 2025 NRR EV Due to Electrical Overheating Risk

    Isuzu is recalling 2025 NRR EV vehicles because a gap in the electrical system may cause overheating and loss of drive power, increasing crash risk.

    Product
    ISUZU — ISUZU NRR EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·015-2025·2025-05-16

    USDA recalls Fijian Import & Export ready-to-eat meat pie products

    Fijian Import & Export Co. Inc. is recalling approximately 127 pounds of ready-to-eat meat pie products imported from Australia that were not presented for FSIS import reinspection. The products were shipped to Rutter's convenience stores in Pennsylvania.

    Product
    Fijian Import & Export Co. Inc. Recalls Ready-To-Eat Meat Pie Products Imported Without Benefit of Import Reinspection
    Category
    Food
    Distribution
    1 state
  • CriticalCPSC·25285·2025-05-15

    Chill Pill Magnetic Haptic Fidget Toys recalled due to ingestion hazard

    FidgetThings is recalling Chill Pill Magnetic Haptic Fidget Toys Red Bumpy because they violate federal magnet regulations and pose a risk of serious injury or death if swallowed by children.

    Product
    Chill Pill Magnetic Haptic Fidget Toys Red Bumpy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25286·2025-05-15

    Child Safety Gates Recalled for Entrapment and Fall Hazards

    Multiple child safety gates sold on Amazon.com violate federal safety regulations, posing risk of serious injury or death from entrapment and falls. Consumers should stop using the gates immediately and contact the seller for disposal and refund.

    Product
    Child Safety Gates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25279·2025-05-15

    NICREW Submersible RGB LED Lights Recalled for Coin Battery Ingestion Hazard

    NICREW 15" Submersible RGB LED Lights with remote controls are recalled because the remote's lithium coin battery can be easily accessed by children, creating a serious ingestion hazard that can cause internal burns and death.

    Product
    NICREW 15" Submersible RGB LED Lights with remote controls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25280·2025-05-15

    Digital Wall Clocks recalled for ingestion hazard from coin battery

    Leon Rading Co. Ltd. is recalling digital wall clocks (model PH-05) sold on Amazon because the remote control contains a lithium coin battery that children can easily access and swallow, risking serious internal injury or death.

    Product
    Digital Wall Clocks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V323000·2025-05-15

    School bus parking brake can release while wheelchair lift is deployed

    International is recalling certain 2025-2026 IC Bus CESB school buses because the parking brake can be released while the wheelchair platform lift is deployed, failing FMVSS 403.

    Product
    IC BUS — IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V269000·2025-05-15

    Volkswagen ID. Buzz third-row bench seats three but has two belts

    Volkswagen is recalling certain 2025 ID. Buzz vehicles because the third-row bench is wide enough for three passengers but is designed for two and has only two seat belts, failing FMVSS 208.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID. BUZZ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25282·2025-05-15

    LivingCaring Adult Portable Bed Rails recalled for entrapment and asphyxiation risk

    LivingCaring Adult Portable Bed Rails pose a serious risk of entrapment and asphyxiation due to violations of federal safety regulations. About 280 units sold online May 2024–March 2025 are affected; consumers should stop using them immediately.

    Product
    LivingCaring Adult Portable Bed Rails
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25281·2025-05-15

    PlayTab Rollers Tile Toys Recalled for Magnet Ingestion Hazard

    Fat Brain Toy Co. is recalling PlayTab Rollers Tile Toys because they contain magnets that can become loose and be swallowed by children, posing a risk of serious injury or death.

    Product
    PlayTab Rollers Tile Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25278·2025-05-15

    Boyro Baby Convertible High Chairs Recalled for Fall and Entrapment Hazards

    Boyro Baby Convertible High Chairs sold on Amazon.com pose a risk of serious injury or death from falls and entrapment. The restraint system is not properly attached and can fail, and the opening between seat and tray is large enough for a child to become trapped.

    Product
    Boyro Baby Convertible High Chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1662-2025·2025-05-14

    CADD Solis HSPCA Pump wireless connection alarm interruption recall

    Smiths Medical is recalling CADD Solis HSPCA Pumps with wireless connection modules that may experience intermittent connection alarms, interrupting active infusions and risking serious patient injury or death.

    Product
    CADD Solis HSPCA Pump ***Updated 5/27/26*** Scope updated to apply specifically to customers using the wireless system. Affected products associated with the change in scope: PUMP KIT, CADD SOLIS HPCA, MDL 2110, V4.3, ENGLISH, 1/EA 21-2111-0403-51 PUMP KIT, CADD SOLIS HPCA, MDL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1667-2025·2025-05-14

    CADD-Solis Ambulatory Infusion Pump False Alarm Malfunction

    Smiths Medical is recalling CADD-Solis and CADD-Solis VIP ambulatory infusion pumps because they may trigger a false upstream occlusion alarm that interrupts therapy, risking serious patient injury or death.

    Product
    CADD-Solis HPCA Ambulatory Infusion Pump; Model/Number: 21-2111-0402-09-KYO 21-2111-0402-09-KYO CADD SOLIS PIB PUMP FOR CLINICAL EVALUATION/DEMO PUMP 21-2111-0300-09_LOAN CADD SOLIS PIB PUMP FOR CLINICAL EVALUATION/DEMO PUMP FOR CMSA 21-2111-0300-09_CMSA CADD Solis PIB PUMP FOR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1668-2025·2025-05-14

    CADD-Solis VIP Ambulatory Infusion Pump False Occlusion Alarm Recall

    Smiths Medical is recalling CADD-Solis VIP Ambulatory Infusion Pumps due to false Upstream Occlusion Alarms that may interrupt medication infusions, risking serious patient injury or death.

    Product
    CADD-Solis VIP Ambulatory Infusion Pump; Model/Number: 21-2120-0100-02 21-2120-0100-03 21-2120-0100-06 21-2120-0100-232 21-2120-0100-233 21-2120-0100-50 21-2120-0100-51 21-2120-0100-95 21-2120-0102-02 21-2120-0102-03 21-2120-0102-06 21-2120-0102-07 21-2120-0102-0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1717-2025·2025-05-14

    CODMAN Craniotomy Kit Cranial Perforator Disposed Over Weld Defect

    Integra LifeSciences is recalling CODMAN Craniotomy Kits due to inadequate welds that may cause the product to disassemble. The defect affects 1,840 units distributed worldwide.

    Product
    CODMAN Craniotomy Kit, Disposable Perforator Cranio-blade Wire Pass Drill, 14mm. Cranial perforator kit.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0402-2025·2025-05-14

    Ropivacaine Hydrochloride Injection Recalled for Particulate Matter

    Amneal Pharmaceuticals is recalling Ropivacaine Hydrochloride Injection 0.5% due to the presence of particulate matter. The recall affects specific lots distributed nationwide.

    Product
    ROPIVACAINE HYDROCHLORIDE — ROPIVACAINE HYDROCHLORIDE (ROPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide