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 the agency’s own highest classification or reported deaths or serious injuries, 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

2201–2225 of 90251

  • SevereFDA (Devices)·Z-2160-2026·2026-06-03

    RelayPro thoracic stent-graft clasp may not release from delivery system

    The RelayPro Thoracic Stent-Graft System is subject to a labeling update concerning proximal clasp disconnection from the outer control tube, which may prevent release of the graft.

    Product
    RelayPro Thoracic Stent-Graft System (various sizes) Reference numbers: 28-N4-32-104-32U 28-N4-32-164-28U 28-N4-32-164-32U 28-N4-32-209-28U 28-N4-32-209-32U 28-N4-32-259-32U 28-N4-34-109-34U 28-N4-34-154-30U 28-N4-34-154-34U 28-N4-34-209-30U 28-N4-34-209-34U 28-N4-34-259-34U…
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2238-2026·2026-06-03

    Automated Impella Controllers recalled over alarm, power and purge cassette faults

    Automated Impella Controllers sold outside the US are being recalled over alarm failures, power-path faults, electrical-short risks, inaccurate motor-current sensing and purge cassette misalignment.

    Product
    Automated Impella Controller (AIC) with the below product descriptions and corresponding Product Codes. 1. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 2. Impella Controller, Packaged, EU; Product Code: 0042-0000-EU. 3. Impella Controller, Packaged…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0850-2026·2026-06-03

    Legacy Bakehouse butter parsley bagel crisps made with recalled milk powder

    Butter Parsley Bagel Crisps from Legacy Bakehouse are being recalled because they were made with recalled California Dairies milk powder over Salmonella.

    Product
    Butter Parsley Bagel Crisps, Item Number 18490, Net Weight: 10 lbs. Legacy Bakehouse, LLC, N8W22100 Johnson Dr., Waukesha, WI 53166.
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Devices)·Z-2231-2026·2026-06-03

    Medline anesthesia trays recalled over Huons bupivacaine quality concerns

    Medline anesthesia trays containing Huons Bupivacaine HCl in Dextrose Injection are being recalled after that drug was recalled. 1,100 kits are affected.

    Product
    Medline kits containing Huons Co. Bupivacaine HCL in Dextrose Injection, USP, labeled as: 1) ANESTHESIA TRAY, Medline SKU DYNJRA1355A; 2) SPINAL ANESTHESIA TRAY, Medline SKU DYNJRA2151.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2211-2026·2026-06-03

    Automated Impella Controllers await four pending hardware safety updates

    Automated Impella Controllers that have not been through Abiomed's servicing process are pending four hardware updates addressing motor control, startup and pump stop risks.

    Product
    Automated Impella Controller (AIC); Product Code: 0042-0000-US;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0856-2026·2026-06-03

    Wawa diet lemon iced tea pints recalled over undeclared milk

    Wawa Diet Iced Tea Lemon in 16 oz plastic bottles is being recalled because of an undeclared milk allergen. 616 units are affected.

    Product
    Wawa Diet Iced Tea Lemon Pint (16oz),Plastic bottle
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·H-0852-2026·2026-06-03

    Giant Eagle pita chips made with recalled California Dairies milk powder

    Giant Eagle Baked Pita Chips with Parmesan, Garlic & Herb Bagel Crisps are being recalled because they were made with recalled California Dairies milk powder over Salmonella.

    Product
    giant eagle Baked Pita Chips with Parmesan, Garlic & Herb Bagel Crisps, Net Wt 7.33 oz. Shipping Case: 12 ct - 7.33 oz Bags Net Weight: 5.49 lbs. Legacy Bakehouse, LLC, Waukesha WI 53186.
    Category
    Food
    Distribution
    2 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 (Food)·H-0854-2026·2026-06-03

    Fly By Jing creamy sesame noodles may contain undeclared peanut

    Fly By Jing Creamy Sesame Noodles are being recalled because possible cross-contamination resulted in an undeclared peanut allergen. 3,419 cases are affected.

    Product
    Fly By Jing (branded) Creamy Sesame Noodles; 3.8 oz packets. Sold in single and 4 packs. Single UPC: 8-50052-23988-6 4 pack UPC: 8-50052-23991-6
    Category
    Food
    Distribution
    Distributed nationwide
  • 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-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-2258-2026·2026-06-03

    Philips Azurion system hard drives may degrade and lose imaging

    Philips Azurion interventional X-ray systems are being recalled because hard drives in the system PCs may lose performance as they age, potentially causing loss of imaging functionality.

    Product
    Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064, 722222), Azurion 5 M12 (722227), Azurion 5 M20 (722228), Azurion 7 B12 (722067, 722225), Azurion 7 B20 (722068, 722226), Azurion 7 M12 (722078, 722223), Azurion 7 M20…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • 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-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
  • 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-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-2259-2026·2026-06-03

    Philips Allura system hard drives may degrade and lose imaging

    Philips Allura Xper interventional X-ray systems are being recalled because hard drives in the system PCs may lose performance as they age, potentially causing loss of imaging functionality.

    Product
    Allura system; System Code Description (Model Numbers): Allura Xper FD10 (722003, 722010, 722026), Allura Xper FD10 OR Table (722022, 722033), Allura Xper FD10/10 (722005, 722011, 722027), Allura Xper FD20 (722006, 722012, 722028), Allura Xper FD20 Biplane (722008, 722013)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V361000·2026-06-03

    Jayco Recalls 2026 Recreational Vehicles Due to Taillight Warning Light Defect

    Jayco is recalling 2026 Entegra and Jayco recreational vehicles because the taillight warning light may illuminate incorrectly, potentially confusing drivers and increasing crash risk.

    Product
    JAYCO — JAYCO, ENTEGRA MELBOURNE, GRANITE RIDGE, QWEST SE, CONDOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • 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-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
  • 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·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, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide