The Recall Desk

Severity 4 of 5

Severe recalls

Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

276–300 of 6113

  • SevereFDA (Devices)·Z-1719-2026·2026-04-15

    Medline Angiographic Syringe Kits Recalled for Potential Adapter Disconnection

    Medline Industries is recalling medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes that may unwind during use, causing loose or complete disconnection between the syringe and manifold.

    Product
    Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. NON VASCULAR PACK, Medline SKU # DYNJ68037C; 2. VEIN, Medline SKU # DYNJ89845; 3. VEIN, Medline SKU # DYNJ89845A.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1729-2026·2026-04-15

    Medline Medical Kits with Angiographic Syringe Adaptors at Disconnection Risk

    Medline is recalling 108 units of medical kits containing angiographic syringe adaptors that may unwind during use, potentially causing disconnection from the manifold.

    Product
    Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: TAVR PACK, Medline SKU # DYNJ84472
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1725-2026·2026-04-15

    Medline NAMIC Angiographic Rotating Adaptor Control Syringes May Disconnect

    Medline Industries is recalling medical convenience kits containing NAMIC Angiographic Rotating Adaptor Control Syringes because the syringe adaptor may unwind during use, potentially causing a loose or complete disconnection from the manifold.

    Product
    Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: GLOVE PACK 7.0 (15PK), Medline SKU # DYNJ63673D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1721-2026·2026-04-15

    Medline Medical Kits With Faulty Syringe Adaptors Recalled

    Medline Industries is recalling 594 medical convenience kits containing NAMIC syringe rotating adaptors that may unwind and disconnect during use. The kits were distributed worldwide.

    Product
    Medline medical convenience kits, containing NAMIC Angiographic Rotating Adaptor (RA) Control Syringes (Namic RA syringes), labeled as follows: 1. HEAD AND NECK CDS-LF, Medline SKU # CDS780138K; 2. HEART CATH PACK-LF, Medline SKU # DYNJ36478B; 3. HEART CATH PACK-LF, Medlin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V869000·2026-04-12

    2025-2026 Toyota Camry and Corolla Cross Hybrid Inverter Defect Recall

    Toyota is recalling approximately 55,405 Camry and Corolla Cross Hybrid vehicles due to a loose inverter bolt that may cause loss of power or fire risk.

    Product
    TOYOTA — 2025 TOYOTA CAMRY HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V704000·2026-04-10

    2025 Chevrolet Equinox EV tires recalled for potential tread detachment

    General Motors is recalling 2025-2026 Chevrolet Equinox EV vehicles equipped with Continental 21-inch tires that may experience tread detachment, increasing crash risk. Dealers will replace affected tires at no cost.

    Product
    CHEVROLET — 2025 CHEVROLET EQUINOX EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26385·2026-04-09

    BISSELL steam cleaners recalled due to burn hazard from detaching attachments

    BISSELL is recalling about 1.7 million Steam Shot steam cleaners because attachments can unexpectedly detach and expel hot water or steam, causing burns. 206 incidents have been reported, including 161 burn injuries.

    Product
    Steam Shot OmniReach and Steam Shot Omni Steam Cleaners with attachments
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0640-2026·2026-04-08

    Spray Dried Dairy Powder recalled due to Salmonella contamination

    Lone Star Dairy Products LLC is recalling Spray Dried Dairy Powder in 25 kg bags and 1 metric ton totes due to Salmonella identification in finished product testing.

    Product
    Spray Dried Dairy Powder 25 kg bags or 1 metric ton totes
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·H-0661-2026·2026-04-08

    Imu-Tek Colostrum-5 Powder Recalled Due to Under-Processing Risk

    Imu-Tek Animal Health has recalled Imu-Tek Colostrum-5 Powder because the product may be under-processed. The recalled lot was distributed across 29 states.

    Product
    Imu-Tek Colostrum-5 Powder; 30% IgG,1,000 mg 2x/day, orally with 8 ounces of water, support a healthy immune system, 3 year shelf life, plastic bottle, inner liner seal and shrink band exterior seal, 24 ounces (680 grams) powder, 7 38654 00052 6, ImuTek Laboratories, Fort Collins
    Category
    Food
    Distribution
    30 states
  • SevereFDA (Drugs)·D-0478-2026·2026-04-08

    IV Bags Labeled as Magnesium Sulfate Actually Contain Tranexamic Acid

    Amneal Pharmaceuticals is recalling Magnesium Sulfate in Water for Injection IV bags labeled as magnesium sulfate, but actually containing tranexamic acid instead. This product mix-up could cause patients to receive the wrong medication.

    Product
    MAGNESIUM SULFATE — MAGNESIUM SULFATE (MAGNESIUM SULFATE IN WATER FOR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1647-2026·2026-04-08

    Home Ventilator Alarm May Fail to Detect Airway Obstruction Promptly

    The Philips Respironics Trilogy Evo O2 ventilator's obstruction alarm may not trigger promptly, taking up to four breaths to respond. This delay could prevent timely detection of a blocked airway in patients depending on the device for breathing support.

    Product
    Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1648-2026·2026-04-08

    Philips Respironics Trilogy EV300 Ventilator Recall: Obstruction Alarm Delay

    Philips Respironics Trilogy EV300 ventilators are recalled because the obstruction alarm may not trigger within required timeframes, potentially delaying detection of airway blockages. Over 113,000 units are affected worldwide.

    Product
    Philips Respironics Trilogy EV300, Software Version 1.05.15.00. Continuous home-use ventilator device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1646-2026·2026-04-08

    Home Ventilator Obstruction Alarm May Fail to Trigger Promptly

    The Philips Respironics Trilogy Evo home ventilator's obstruction alarm may not trigger within required timeframes, potentially delaying detection of airway blockages. Approximately 113,717 units are affected worldwide.

    Product
    Philips Respironics Trilogy Evo, Software Version 1.05.15.00. Continuous home-use ventilator device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1589-2026·2026-04-08

    Purge Cassettes May Leak in Impella Pump and Assist Sets

    Abiomed is recalling Purge Cassettes used in Impella pump systems worldwide due to increased risk of purge leaks. The cassettes are included in multiple pump set models distributed across 33,107 units.

    Product
    Purge Cassette, sold within Impella Pump Sets and Individually Packaged. Labeled and distributed in the below configurations and corresponding product codes. 1. Purge Cassette, 5 Pack; Product Code: 0043-0003. 2. Impella RP US Pump Set; Product Code: 004334. 3. Purge C
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1591-2026·2026-04-08

    Impella Controller Purge System Alarm Display May Be Delayed

    The FDA is recalling Automated Impella Controllers because the 'Purge System Blocked' alarm display may be delayed when using first generation Impella 5.5 pumps, potentially delaying notification of blockage.

    Product
    Automated Impella Controller (AIC), labeled as the following with 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, UK; Produc
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1637-2026·2026-04-08

    Blue Ventilator Adapter Module Correction for Oxygen Desaturation Risk

    Baxter Healthcare issued a Class I correction for the Blue Ventilator Adapter Module (Volara system accessory) due to potential oxygen desaturation and lung tissue injury risk in home care settings. Specific instructions for use are being provided.

    Product
    Blue Ventilator Adapter Module, single-patient use circuit, Product Code M07937. Accessory to Baxter Volara Respiratory Therapy system.
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1649-2026·2026-04-08

    Philips Respironics Trilogy Evo Universal Ventilator Obstruction Alarm Delay Recalled

    Philips Respironics Trilogy Evo Universal ventilator software version 1.05.15.00 recalled because the obstruction alarm may fail to trigger within required timeframes, potentially delaying critical responses to airway obstruction.

    Product
    Philips Respironics Trilogy Evo Universal, Software Version 1.05.15.00. Continuous home-use ventilator device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V238000·2026-04-03

    2024 Chrysler Pacifica and Voyager Windshield Detachment Recall

    Chrysler is recalling 223 2024 Pacifica and Voyager vehicles because the windshield may not be properly bonded and could detach during a crash, creating an injury risk. Dealers will replace the windshield at no cost.

    Product
    CHRYSLER — 2024 CHRYSLER PACIFICA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V237000·2026-04-03

    2023 GMC Canyon recalled for damaged front wheel hub bolts

    General Motors is recalling 2023 GMC Canyon vehicles because front wheel hub bolts may have been damaged during installation. Damaged bolts could loosen or break, potentially causing loss of vehicle control and increasing crash risk.

    Product
    GMC — 2023 GMC CANYON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26379·2026-04-02

    HTRC and Haisito T400 battery chargers recalled for fire hazard

    HTRC and Haisito model T400 battery chargers are being recalled due to fire and explosion hazards. The chargers can ignite or cause connected batteries to ignite, resulting in risk of serious injury and death.

    Product
    HTRC and Haisito battery chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26382·2026-04-02

    Samson International Canopy Bed Frames Recalled for Collapse Hazard

    Samson International recalls 5,600 Universal Broadmoore canopy bed frames. The canopy beams can collapse when moved, causing impact injuries. Five collapses have been reported, with four resulting in shoulder and head contusions.

    Product
    Universal Broadmoore brand Bellevue and Oaklynn model canopy bed frames
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26377·2026-04-02

    Granitestone Diamond Pro Blue Sauté Pans Recalled for Detaching Metal Caps

    About 740,000 Granitestone Diamond Pro Blue sauté pans are recalled because metal caps can detach and forcefully eject when heated, posing burn and impact hazards. One injury has been reported.

    Product
    Granitestone Diamond Pro Blue Sauté Pans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0618-2026·2026-04-01

    Basil Pesto and Mozzarella Pizza recalled for metal fragments

    Bakkavor is recalling Basil Pesto & Mozzarella Pizza due to metal fragments discovered in the product. The contamination originated from roasted tomatoes supplied by an ingredient supplier.

    Product
    Basil Pesto & Mozzarella Pizza NET WT. 13.90OZ (394g) UPC 8 57919 00785 5 Distributed by: Grocery Delivery E-Services New York, NY 10005
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·H-0647-2026·2026-04-01

    SiluetaYa Mexican Tejocote Roots Supplement Pieces Recalled for Yellow Oleander

    SiluetaYa Mexican Tejocote Roots Supplement Pieces (7g bottles, Lot US1220) are recalled because the product contains yellow oleander, a toxic substance. The product was distributed online to consumers in AZ, CA, NM, NY, TX, and UT.

    Product
    SiluetaYa Mexican Tejocote Roots Supplement Pieces; 7g/bottle; Dietary Supplement, UPC#: 7500464462411, Lot: US1220 " Expiration Date: 06/2027
    Category
    Food
    Distribution
    6 states