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

Agency

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

1576–1600 of 89454

  • HighFDA (Devices)·Z-2242-2026·2026-06-03

    GE CARESCAPE v5 telemetry servers may lose patient monitoring signal

    GE HealthCare is recalling CARESCAPE Telemetry Server V5 ATO models because a persistent NO COMM or OFF NETWORK condition can cause potential loss of ECG and SpO2 monitoring.

    Product
    GE HealthCare CARESCAPE TELEMETRY SERVER V5 ATO MODEL, REF #2063702-101, Product Code SS9; used in conjunction with ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2246-2026·2026-06-03

    GE CARESCAPE telemetry servers may lose ECG and SpO2 monitoring

    GE HealthCare is recalling trade-in CARESCAPE Telemetry Servers because a persistent NO COMM or OFF NETWORK condition can cause potential loss of ECG and SpO2 monitoring.

    Product
    GE HealthCare TRADE IN CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603-902, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2260-2026·2026-06-03

    Medline eye trays contain insulin syringes labeled as tuberculin syringes

    Medline EYE TRAY-LF kits are being recalled because they contain Cardinal Health syringes packaged as 1 mL tuberculin syringes but which are actually U-100 insulin syringes.

    Product
    Medline medical convenience kit labeled as EYE TRAY-LF, Medline Kit SKU DYNJ21627P
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2243-2026·2026-06-03

    GE ApexPro disaster recovery USB kits may lose patient monitoring

    GE HealthCare ApexPro v5.0 Software Disaster Recovery USB Kits are being recalled because a persistent NO COMM or OFF NETWORK condition can cause loss of ECG and SpO2 monitoring.

    Product
    GE HealthCare APEXPRO v5.0 - ARK2250 - Software Disaster Recovery USB Kit - Orderable by GE Service only, REF #2108523-01; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2239-2026·2026-06-03

    HydroMARK breast biopsy markers may carry the wrong inner labeling

    HydroMARK Breast Biopsy Site Markers are being recalled because boxes labeled as T3 markers may contain individual packages labeled as T4 markers. 1,910 units are affected.

    Product
    HydroMARK Breast Biopsy Site Marker, Model Number: 4010-02-15-T3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2244-2026·2026-06-03

    GE CARESCAPE IOU assembly may lose ECG and SpO2 monitoring

    GE HealthCare IOU assemblies for the ARK2250 CARESCAPE Telemetry Server are being recalled because a persistent NO COMM or OFF NETWORK condition can cause loss of monitoring.

    Product
    GE HealthCare IOU ASSY ARK2250 CARESCAPE TELEMETRY SERVER, REF #2108729-901, Product Code SS9; ApexPro CARESCAPE Telemetry Server (CTS) v5.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2247-2026·2026-06-03

    GE ApexPro v6.0 software may lose ECG and SpO2 monitoring

    GE HealthCare ApexPro v6.0 eDelivery Software is being recalled because a persistent NO COMM or OFF NETWORK condition can cause potential loss of ECG and SpO2 monitoring.

    Product
    GE HealthCare ApexPro v6.0 eDelivery Software, REF #5700026, Product Code SUV; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2230-2026·2026-06-03

    Halyard nitrile exam gloves failed chemical permeation performance specifications

    Halyard Purezero Ultraviolet Nitrile Exam Gloves are being recalled because they failed to meet specifications for chemical permeation performance. 452,500 units are affected.

    Product
    Halyard Purezero Ultraviolet Nitrile Exam Gloves Reference Numbers: 48771 (XS), 48772 (Sm.), 48773 (Md.), 48774 (Lg.), 48775 (Xl)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2245-2026·2026-06-03

    GE CARESCAPE ARK-2250L telemetry servers may lose patient monitoring

    GE HealthCare CARESCAPE Telemetry Servers ARK-2250L are being recalled because a persistent NO COMM or OFF NETWORK condition can cause potential loss of ECG and SpO2 monitoring.

    Product
    GE HealthCare CARESCAPE TELEMETRY SERVER ARK-2250L - NORTH AMERICA, REF #5697603, Product Code KSA; used in conjunction wtih ApexPro CARESCAPE Telemetry Server (CTS) v6.0; Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·26V355000·2026-06-02

    Nova Bus Recalls LFS Transit Buses Due to Brake Warning Light Defect

    Nova Bus is recalling LFS and LFS Artic transit buses because the low brake air pressure warning light may fail to illuminate when the engine is off, increasing crash risk.

    Product
    NOVA BUS — NOVA BUS LFS ARTIC, LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V358000·2026-06-02

    Chrysler Recalls Pacifica and Voyager Models Due to Air Bag Defect

    Chrysler is recalling 2023-2026 Pacifica and Voyager vehicles because a spring may prevent air bags from deploying, increasing injury risk.

    Product
    CHRYSLER — CHRYSLER PACIFICA, VOYAGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V356000·2026-06-02

    Kia Recalls 2027 Telluride Models for Seat Belt Retraction Defect

    Kia is recalling 2027 Telluride and Telluride Hybrid vehicles because the driver seat belt may fail to extend, increasing injury risk in a crash.

    Product
    KIA — KIA TELLURIDE HYBRID, TELLURIDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·007-2026·2026-05-31

    Synear frozen pork and crab soup dumplings contain undeclared peanut

    Synear Foods is recalling about 71,603 pounds of frozen pork and crab soup dumplings because the products were formulated with peanut oil but peanuts were not declared on the label.

    Product
    Synear Foods USA, LLC — Synear Foods USA, LLC Recalls Frozen Pork and Crab Soup Dumpling Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    3 states
  • HighNHTSA·26V352000·2026-05-29

    Forest River travel trailer fireplace outlets may have incorrect wiring

    Forest River is recalling certain 2024-2026 Wildwood and Salem travel trailers because the fireplace outlet may have incorrect wiring, increasing the risk of a fire.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM, STEALTH EVO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V353000·2026-05-29

    2026 Mercedes-Benz and Maybach Models Rear Seat Belt Recall

    Mercedes-Benz USA is recalling 2026 GLS, GLE, and Maybach models due to rear seat belt bolts that may not be properly tightened, reducing restraint effectiveness in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH, MERCEDES BENZ GLE 450 4MATIC, GLS 600 4MATIC, GLE 350, GLE 350 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·26515·2026-05-28

    Anzmtosn Luminous Fidget Spinner Balls Recalled for Battery Ingestion Risk

    Anzmtosn Luminous Fidget Spinner Balls are recalled because the included mini flashlight contains easily accessible button cell batteries that can cause serious internal injuries or death if swallowed by children.

    Product
    Anzmtosn Luminous Fidget Spinner Balls
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·26508·2026-05-28

    MiniWarGaming and Primal Horizon Disc Magnets Violate Mandatory Safety Standard

    MiniWarGaming Inc. and Primal Horizon are recalling approximately 22,624 disc magnets that violate mandatory safety standards. The high-powered magnets pose a deadly ingestion hazard to children.

    Product
    MiniWarGaming and Primal Horizon Disc Magnets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V348000·2026-05-28

    IC Bus Recalls 2026-2027 EVSB School Buses for Drive Motor Bolt Issue

    International Motors is recalling 2026-2027 IC Bus EVSB school buses because improperly tightened bolts may allow the drive motor to detach, creating a road hazard.

    Product
    IC BUS — IC BUS EVSB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26506·2026-05-28

    Giantex and Costway Portable Steam Saunas Recalled for Burn Hazard

    Giantex and Costway portable steam saunas are recalled because the steam diffuser can position too close to the user's body, causing burns. Giantex has received nine burn reports, including one second-degree burn.

    Product
    Giantex and Costway 2-liter and 3-liter Portable Steam Saunas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V351000·2026-05-28

    Mack Trucks Recalls 644 Vehicles Due to Wheel Lug Nut Loosening Risk

    Mack Trucks is recalling 644 vehicles because wheel lug nuts may loosen, allowing the wheel to detach. Owners are advised not to drive until repairs are completed.

    Product
    MACK — MACK GRANITE (GR), ANTHEM AN (4), PINNACLE (PI/PN), ANTHEM (AN)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26513·2026-05-28

    Joy Furniture Recalls Talan and Royce Living Room Furniture Sets

    Joy Furniture is recalling about 10,400 Talan and Royce sofas, loveseats, and recliners due to a fire hazard in the power switch that can overheat. The firm has reported 41 incidents including smoking, burning, and two fires, with no injuries reported so far.

    Product
    Talan and Royce Collection Sofas, Loveseats and Recliners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26514·2026-05-28

    Misco Sports Light-Up Racket Sets Recalled for Battery Ingestion Risk

    Missry Associates recalls Misco Sports Light-Up Racket Sets (model MT2287) because the battery compartment screw can detach and button cell batteries in the shuttlecock can be easily accessed by children, posing risk of serious injury or death if swallowed.

    Product
    Misco Sports Light-Up Racket Sets, model MT2287
    Category
    Consumer Product
    Distribution
    Distributed nationwide