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.

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12976–13000 of 27721

  • SevereFDA (Food)·F-1169-2024·2024-04-24

    H&Natural Brazil Seed Supplement Recalled for Yellow Oleander

    HandNatural is recalling H&Natural Brazil Seed supplement due to the presence of yellow oleander and its components. The product was distributed through internet sales.

    Product
    H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 30 DAYS, 5 GRAMS PER BOX, YELLOW BOX.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1500-2024·2024-04-24

    Philips Garbin EVO Ventilator False Battery Alarm Causes Ventilation Loss

    Philips Respironics recalls 1,233 Garbin EVO ventilators. A software defect in the battery and power alarm system may cause sudden loss of ventilation despite adequate power supply.

    Product
    Garbin EVO, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients. (sold outside US)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1501-2024·2024-04-24

    LifeVentEVO2 Ventilator Recalled for Potential Loss of Ventilation

    Philips Respironics is recalling the LifeVentEVO2 ventilator due to a software malfunction that can trigger a false Battery Depleted or Loss of Power alarm when power is sufficient, potentially causing sudden loss of ventilation.

    Product
    LifeVentEVO2, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients. (sold outside US)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1168-2024·2024-04-24

    H&Natural Brazil Seed supplement recalled for toxic plant contamination

    HandNatural is recalling H&Natural Brazil Seed supplements because the product contains yellow oleander, a toxic plant that poses serious health risks. Consumers should stop using the product immediately.

    Product
    H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 30 DAYS, 5 GRAMS PER BOX, ORANGE BOX.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1521-2024·2024-04-24

    FDA Recalls SonarMed Airway Sensor for Obstruction Detection Failure

    SonarMed Inc is recalling the AW-S035 NEO airway monitoring sensor due to failure to detect partial obstructions. The defect may prevent the device from alerting clinicians to airway obstruction.

    Product
    AW-S035 NEO SONARMED SENSOR 3.5MM. Used in conjunction with SonarMed Monitor for airway monitoring.
    Category
    Medical Device
    Distribution
    19 states
  • SevereFDA (Food)·F-1161-2024·2024-04-24

    H&Natural Tejocote Root Supplement Recalled for Yellow Oleander Contamination

    H&Natural is recalling its tejocote root supplement because the product contains yellow oleander and its components. Consumers should not use this supplement.

    Product
    H&NATURAL TEJOCOTE ROOT 90 PIECES, 3 MONTH SUPPLY, PURE AND NATURAL RAIZ DE TEJOCOTE SUPPLEMENT FOR WOMEN AND MEN.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1485-2024·2024-04-24

    Tablo Hemodialysis System recalled for PCB contamination in tubing

    Outset Medical is recalling Tablo Hemodialysis Systems because their silicone tubing may contain unremoved polychlorinated biphenyl acids (PCBAs), which could cause skin conditions, liver damage, reproductive harm, or cancer.

    Product
    Tablo Hemodialysis System, REF: PN-0003000, PN-0006000 and PN-0007001
    Category
    Medical Device
    Distribution
    42 states
  • SevereFDA (Food)·F-1164-2024·2024-04-24

    HandNatural dietary supplement recalled for yellow oleander contamination

    HandNatural is recalling its Brazil seed dietary supplement because the product contains yellow oleander, a toxic plant substance. This FDA Class I recall poses serious health concerns.

    Product
    H&NATURAL 2 PACK! BRAZIL SEED 30 PIECES, FOR 30 DAYS, 5 GRAMS PER BOX
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1170-2024·2024-04-24

    Brazil seed dietary supplement recalled due to yellow oleander contamination

    HandNatural Brazil seed supplement recalled for containing yellow oleander, a toxic plant. Affected products sold online with expiration dates 05/24 and 03/24.

    Product
    H&NATURAL 2 PACK! BRAZIL SEED 60 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 60 DAYS, 5 GRAMS PER BOX, 2 BLACK BOXES.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1171-2024·2024-04-24

    Herbal dietary supplement recalled for toxic yellow oleander presence

    HandNatural is recalling H&NATURAL BRAZIL SEED, a dietary supplement sold online, due to contamination with yellow oleander, a toxic plant component.

    Product
    H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 30 DAYS, 5 GRAMS PER BOX, BLACK BOX.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1166-2024·2024-04-24

    H&Natural Brazil Seed dietary supplement recalled for yellow oleander

    HandNatural is recalling H&Natural Brazil Seed 30-piece supplements due to the presence of yellow oleander and its components in the product. Consumers should stop using the product immediately and dispose of it safely.

    Product
    H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 30 DAYS, 5 GRAMS PER BOX, BLACK BOTTLE
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1397-2024·2024-04-24

    Elekta Disposable Biopsy Needles Recalled for Microscopic Internal Debris

    Elekta recalled disposable biopsy needles from batch 837838839 that may contain microscopic stainless steel debris inside. The sterility of the needles has not been affected, and this issue has been reported from only one site.

    Product
    Elekta Disposable Biopsy Needle Kit for Leksell Stereotactic System, REF 911933, 2.1mm Diameter / 14 Gauge, containing 6 inner boxes labeled REF 911761, Disposable Biopsy Needle Kit for Leksell Stereotactic System. Each inner box of REF 911761 contains a Tyvek bag labeled REF 91
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1503-2024·2024-04-24

    Trilogy Evo O2 Ventilator Recalled for Potential Sudden Loss of Ventilation

    Philips Respironics is recalling 789 Trilogy Evo O2 ventilators due to a software defect that can trigger a false power alarm despite sufficient power, potentially causing sudden loss of ventilation in pediatric and adult patients.

    Product
    Trilogy Evo O2, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1504-2024·2024-04-24

    Trilogy Evo Ventilator Recall Due to Potential Loss of Ventilation

    Philips Respironics is recalling the Trilogy Evo ventilator (76,713 units) because it may suddenly stop ventilating when a false Battery Depleted or Loss of Power alarm triggers despite sufficient power available.

    Product
    Trilogy Evo, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1172-2024·2024-04-24

    Brazil seed dietary supplement recalled for yellow oleander contamination

    HandNatural's H&Natural Brazil Seed dietary supplement is being recalled due to the presence of yellow oleander, a toxic plant component. Distribution was exclusively through internet sales.

    Product
    H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 30 DAYS, 5 GRAMS PER BOX, ORANGE BOTTLE.
    Category
    Drug
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1499-2024·2024-04-24

    Philips Respironics Aeris EVO Ventilators Recalled for Loss of Ventilation Risk

    Philips Respironics is recalling Aeris EVO ventilators due to a software defect that may cause false battery or power alarms while the device retains adequate power, risking sudden loss of ventilation in pediatric and adult patients. Approximately 775 units are affected.

    Product
    Aeris EVO, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients. (sold outside US)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1178-2024·2024-04-24

    Helados Mexico Ice Cream Minis Recalled for Salmonella

    Tropicale Foods is recalling Helados Mexico Premium Ice Cream Minis due to potential Salmonella contamination. The recall affects 5,224 retail units distributed across six U.S. states.

    Product
    Helados Mexico Premium Ice Cream Minis Variety Pack 12 bars Strawberry, Coconut, Mango 1.5 FL OZ (44mL) Bards Net 18 FL OZ (528mL)
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-1519-2024·2024-04-24

    SonarMed 2.5mm Airway Sensor Recalled for Obstruction Detection Failure

    SonarMed Inc is recalling the AW-S025 NEO SONARMED SENSOR 2.5MM airway monitoring device due to a malfunction that causes it to fail detecting partial obstruction, potentially preventing clinicians from identifying compromised airways.

    Product
    AW-S025 NEO SONARMED SENSOR 2.5MM. Used in conjunction with SonarMed Monitor for airway monitoring.
    Category
    Medical Device
    Distribution
    19 states
  • SevereFDA (Devices)·Z-1505-2024·2024-04-24

    Philips Trilogy Evo Ventilator Recall: Potential Loss of Ventilation Due to False Alarm

    Philips is recalling the Trilogy Evo Universal Ventilator for a software defect that triggers false low-battery or power-loss alarms despite sufficient power, risking sudden ventilation loss.

    Product
    Trilogy Evo Universal Ventilator, all software versions except 1.05.06.00. Ventilator for pediatric and adult patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1535-2024·2024-04-24

    Medical Device Airway Monitor Software Defect Prevents Obstruction Detection

    A software anomaly in SonarMed's AW-M0001 airway monitor prevents detection of partial airway obstructions in 2.5mm and larger sensors. The device may fail to alert clinicians to blockages, affecting approximately 145 units across 19 states.

    Product
    AW-M0001 SONARMED MONITOR. Used in conjunction with SonarMed Acoustic Sensors for airway monitoring.
    Category
    Medical Device
    Distribution
    17 states
  • SevereFDA (Devices)·Z-1512-2024·2024-04-24

    Dräger Perseus A500 Anesthesia Workstation Recalled for Unexpected Battery-Power Shutdowns

    Draeger Medical is recalling approximately 16,841 Dräger Perseus A500 Anesthesia Workstations due to unexpected shutdown while operating on battery power. The devices have been distributed nationwide and internationally.

    Product
    Dr¿ger Perseus A500 Anesthesia Workstation
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1167-2024·2024-04-24

    H&Natural Brazil Seed supplement recalled for yellow oleander contamination

    H&Natural Brazil Seed is a botanical supplement sold online that is being recalled because the product contains yellow oleander and its components. The manufacturer is HandNatural.

    Product
    H&NATURAL BRAZIL SEED 30 PIECES, PURE NATURAL SEMILLA DE BRASIL FOR 30 DAYS, 5 GRAMS PER BOX, YELLOW BOTTLE.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1158-2024·2024-04-24

    H&Natural Tejocote Root Dietary Supplement Recalled Due to Yellow Oleander

    HandNatural is recalling H&Natural Tejocote Root dietary supplement because the product contains yellow oleander and its components, which pose a health risk.

    Product
    H&NATURAL TEJOCOTE ROOT Dietary Supplement Net WT 0.36 oz (10g)
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1159-2024·2024-04-24

    HandNatural Brazil Seeds Recalled for Toxic Yellow Oleander Contamination

    HandNatural Brazil seeds (5g) have been recalled for contamination with yellow oleander, a highly toxic substance. FDA classified this as a Class I recall due to serious health hazards.

    Product
    Brazil Seed Net WT 0.18 oz (5g)
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-1174-2024·2024-04-24

    Great Value Sandwich Cookies Recalled for Plastic Foreign Material

    Shearer's Foods is recalling Great Value Twist & Shout Strawberry Creme Sandwich Cookies due to possible plastic fragments in the product. Affected items have a best-if-used-by date of September 11, 2024.

    Product
    Great Value Twist & Shout Strawberry Creme Sandwich Cookies, Net WT 15.35 oz. box containing film wrapped trays of stacked cookies. 12 boxes per case.
    Category
    Food
    Distribution
    1 state