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.

826–850 of 29054

  • SevereNHTSA·26V238000·2026-04-14

    Ford Recalls 2024-2026 Rangers for Sun Visor Wiring Fire Risk

    Ford is recalling 2024-2026 Ranger vehicles because improperly positioned sun visor or headliner wiring harnesses may cause an electrical short and fire in the A-pillar area.

    Product
    FORD — FORD RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V237000·2026-04-14

    Ford Recalls 2015-2017 F-150 Trucks for Transmission Software Defect

    Ford is recalling 2015-2017 F-150 vehicles because a signal loss can cause unexpected downshifting, increasing crash risk. Dealers will update software free of charge.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V236000·2026-04-14

    Ford Bronco transfer case joint misalignment may wear driveline splines

    Ford is recalling certain 2021-2025 Bronco vehicles because a misaligned transmission to transfer case joint can wear the splines, potentially causing loss of drive power or rollaway.

    Product
    FORD — FORD BRONCO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V234000·2026-04-13

    2025–2026 Harley-Davidson Softail motorcycles rear brake line defect

    Harley-Davidson is recalling certain 2025–2026 Softail motorcycles because the rear brake line may contact the Body Control Module, causing a brake fluid leak and loss of rear brakes. Loss of rear brakes increases crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHC, FXBB, FXLRS, FXLRST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E019000·2026-04-09

    Nova Bus Recalls Ricon Hidden Frame Windows for Detachment Risk

    Nova Bus is recalling Ricon hidden frame windows sold through Prevost due to inadequate adhesion that may cause glass to detach, increasing crash injury risk.

    Product
    VISIBILITY:GLASS, SIDE/REAR:CRITICAL FASTENERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V226000·2026-04-09

    IC Bus Recalls EVSB School Buses Due to High Voltage Switch Defect

    International Motors is recalling 2022-2027 IC Bus EVSB school buses because a high voltage disconnect switch may fail to shut off power, posing a risk of electrical shock.

    Product
    IC BUS — IC BUS EVSB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26372·2026-04-09

    Osprey robotic pool vacuum batteries can overheat and catch fire

    Osprey 700 Max and S1 robotic pool vacuums are recalled because the lithium-ion battery can overheat. Ten reports of overheating or fire have caused nine incidents of property damage; no injuries reported.

    Product
    Osprey 700 Max and S1 robotic pool vacuums
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V227000·2026-04-09

    Honda Odyssey side air bags may deploy unexpectedly from software error

    Honda is recalling certain 2018-2022 Odyssey vehicles because a software programming error can cause the side and side curtain air bags to deploy unexpectedly. 440,830 vehicles are affected.

    Product
    HONDA — HONDA ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V228000·2026-04-09

    Thomas Built Buses Recalls Saf-T-Liner C2 School Buses for Software Defect

    Daimler Trucks North America is recalling 2024-2027 Thomas Built Buses Saf-T-Liner C2 school buses because a software defect may prevent warning lights and the stop sign arm from activating.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26385·2026-04-09

    BISSELL steam cleaner attachments can detach and expel hot water

    BISSELL Steam Shot OmniReach and Omni handheld steam cleaners are recalled after 206 reports of hot water or steam escaping from the attachments, including 161 reports of burn injuries.

    Product
    Steam Shot OmniReach and Steam Shot Omni Steam Cleaners with attachments
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1591-2026·2026-04-08

    Impella controller purge blocked alarm may be delayed on older pumps

    Abiomed is recalling Automated Impella Controllers because the Purge System Blocked alarm display could be delayed when using first generation Impella 5.5 pumps.

    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 (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 (Devices)·Z-1589-2026·2026-04-08

    Impella purge cassettes recalled as Class I over purge leak risk

    Purge Cassettes sold within Impella Pump Sets and individually packaged are being recalled because of an increased risk of purge leaks with Generation 1 purge cassettes.

    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-1647-2026·2026-04-08

    Trilogy Evo O2 obstruction alarm may take up to four breaths

    Philips Respironics is recalling the Trilogy Evo O2 ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.

    Product
    Philips Respironics Trilogy Evo O2, Software Version 1.05.15.00. Continuous home-use ventilator device.
    Category
    Medical Device
    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 (Devices)·Z-1646-2026·2026-04-08

    Trilogy Evo obstruction alarm may take up to four breaths

    Philips Respironics is recalling the Trilogy Evo ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.

    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-1649-2026·2026-04-08

    Trilogy Evo Universal obstruction alarm may take up to four breaths

    Philips Respironics is recalling the Trilogy Evo Universal ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.

    Product
    Philips Respironics Trilogy Evo Universal, 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

    Trilogy EV300 obstruction alarm may take up to four breaths

    Philips Respironics is recalling the Trilogy EV300 ventilator because in some situations the Obstruction Alarm does not trigger within the timeframe required by the relevant standards.

    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-1637-2026·2026-04-08

    Volara ventilator adapter recalled as Class I over desaturation and barotrauma

    Baxter is issuing an urgent correction for the Blue Ventilator Adapter Module used with the Volara system because home users may be unaware of possible oxygen desaturation or lung injury from overexpansion.

    Product
    Blue Ventilator Adapter Module, single-patient use circuit, Product Code M07937. Accessory to Baxter Volara Respiratory Therapy system.
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0478-2026·2026-04-08

    Magnesium sulfate pouch recalled as Class I for containing tranexamic acid

    One lot of Magnesium Sulfate in Water for Injection is being recalled after a foil pouch labeled as magnesium sulfate was found to contain an IV bag of tranexamic acid.

    Product
    MAGNESIUM SULFATE — MAGNESIUM SULFATE (MAGNESIUM SULFATE IN WATER FOR)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V216000·2026-04-03

    Mercedes-Benz Recalls Vehicles for Drive Shaft Universal Joint Breakage Risk

    Mercedes-Benz is recalling specific 2018-2020 E-Class and S-Class models because the drive shaft universal joint may break, causing a sudden loss of drive power and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH E 400 4MATIC WAGON, S 560 4MATIC, S 450 4MATIC, E 450 4MATIC WAGON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26379·2026-04-02

    HTRC and Haisito battery chargers can ignite causing fires

    Huizhou Haitan Technology is recalling T400 battery chargers because they can ignite or cause a connected battery to ignite. Thirty-three fires and explosions have been reported.

    Product
    HTRC and Haisito battery chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide