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.

2076–2100 of 29084

  • SevereNHTSA·25V235000·2025-04-10

    Hyundai IONIQ 5 N may brake weakly and keep accelerating

    Hyundai is recalling certain 2025 IONIQ 5 N vehicles because software may reduce braking performance with left-foot braking active and the vehicle may continue to accelerate.

    Product
    HYUNDAI — HYUNDAI IONIQ 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V232000·2025-04-10

    Cadillac LYRIQ stabilizer bar bracket bolts may loosen and separate

    GM is recalling certain 2023-2025 Cadillac LYRIQ vehicles because front stabilizer bar bracket bolts may loosen and separate from the vehicle frame.

    Product
    CADILLAC — CADILLAC LYRIQ
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1495-2025·2025-04-09

    Draeger Anesthesia Circuit Kit Flex 1 recalled for potential hose cracks

    Draeger, Inc. is recalling Anesthesia Circuit Kit Flex 1 devices nationwide and internationally due to potential cracks in the breathing circuit hose that conducts anesthesia gases.

    Product
    Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 1 Model/Catalog Number: MP02737 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1493-2025·2025-04-09

    VentStar Flex 220 Breathing Circuit Recalled for Potential Hose Cracks

    Draeger, Inc. is recalling 65,150 units of the VentStar Flex 220 breathing circuit due to the potential for cracks to form in the hose. A crack could affect gas delivery during anesthesia or ventilation procedures.

    Product
    Brand Name: VentStar Product Name: VentStar Flex 220 Model/Catalog Number: MP00355 Software Version: Not applicable Product Description: Breathing circuit for conveying breathing gases between an anesthesia machine or ventilator and adult patients. The breathing circuit is in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0679-2025·2025-04-09

    Choshiya Rakkyo Zuke Prepared Vegetables Recalled for Missing Refrigeration Label

    Choshiya brand rakkyo zuke prepared vegetables are being recalled due to missing 'Keep Refrigerated' label statements. These non-shelf-stable vegetables may spoil if not properly refrigerated.

    Product
    Choshiya branded "RAKKYO ZUKE PREPARED VEGETABLES" UPC# JANCODE 4983673526021
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1496-2025·2025-04-09

    Anesthesia Circuit Kit Flex 2 recalled due to breathing hose crack risk

    Draeger's Anesthesia Circuit Kit Flex 2 is recalled because of the potential for cracks to form in the breathing circuit hose. No injuries have been reported.

    Product
    Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 2 Model/Catalog Number: MP02738 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1499-2025·2025-04-09

    Anesthesia Circuit Kit Flex EPA recalled due to breathing hose cracking

    Draeger is recalling the Anesthesia Circuit Kit Flex EPA due to the potential for cracks to form in the breathing circuit hose. Approximately 13,620 units have been distributed domestically and internationally. Users should discontinue use of affected units immediately.

    Product
    Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex EPA Model/Catalog Number: MP17103 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intend
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1494-2025·2025-04-09

    Draeger ID Circuit Flex 220 breathing circuit hoses subject to cracking

    Draeger's ID Circuit Flex 220 breathing circuit for anesthesia machines may develop cracks in the hose. The recall affects 3,325 units distributed nationwide and internationally.

    Product
    Brand Name: ID Circuit Product Name: ID Circuit Flex 220 Model/Catalog Number: MP01347 Software Version: Not applicable Product Description: Breathing circuit for conveying breathing gases between an anesthesia machine or ventilator and adult Component: Not applicable
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1497-2025·2025-04-09

    Anesthesia Circuit Kit Flex 6 Recalled for Potential Breathing Hose Cracks

    Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex 6 (Model MP02744) due to potential cracks forming in the breathing circuit hose. Approximately 293,660 units were distributed nationwide and internationally.

    Product
    Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex 6 Model/Catalog Number: MP02744 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is intended
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V216000·2025-04-09

    McLaren brake lines may be routed to the wrong side

    McLaren is recalling certain 2020-2025 vehicles because brake lines may be routed incorrectly, activating the brakes on the wrong side and possibly locking a rear wheel.

    Product
    MCLAREN — MCLAREN ARTURA, 720S SPIDER, GT, 600LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0675-2025·2025-04-09

    Choshiya Shiba Zuke Prepared Mix Vegetables Recalled for Missing Refrigeration Label

    AKT Trading Inc. is recalling Choshiya branded Shiba Zuke Prepared Mix Vegetables (1,000 cases) because they are missing the required "Keep Refrigerated" statement on the label. Non-shelf stable vegetables could be improperly stored without this critical labeling information.

    Product
    Choshiya branded "SHIBA ZUKE PREPARED MIX VEGETABLES" UPC# JANCODE 4582207535128
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0678-2025·2025-04-09

    Packaged Vegetables Recalled for Missing Refrigeration Label Statement

    AKT Trading Inc. is recalling Choshiya branded Soft Tsubozuke Prepared Mix Vegetables due to missing "Keep Refrigerated" statement on labels. Non-shelf stable vegetables lacking this statement may spoil or develop harmful bacteria if stored improperly.

    Product
    Choshiya branded "SOFT TSUBOZUKE PREPARED MIX VEGETABLES" UPC# JANCODE 4582207535159
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0676-2025·2025-04-09

    Choshiya Aokappa Zuke Prepared Mix Vegetables Recalled for Missing Refrigeration Label

    AKT Trading Inc. is recalling Choshiya branded Aokappa Zuke Prepared Mix Vegetables because the product label lacks a 'Keep Refrigerated' statement, risking improper storage of non-shelf-stable vegetables.

    Product
    Choshiya branded "AOKAPPA ZUKE PREPARED MIX VEGETABLES" UPC# JANCODE 4582207535135
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0680-2025·2025-04-09

    Choshiya Prepared Bamboo Shoots Recalled Due to Missing Keep Refrigerated Label

    Choshiya branded menma (prepared bamboo shoots) are being recalled because the label fails to include the required 'Keep Refrigerated' statement. Improper storage of this non-shelf-stable product could lead to foodborne illness.

    Product
    Choshiya branded "MENMA AJITSUKE PREPARED BAMBOO SHOOTS" UPC# JANCODE 4983673527325
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-0688-2025·2025-04-09

    Tostitos Cantina Chips Recalled for Undeclared Milk Allergen

    Frito-Lay is recalling 1,295 bags of Tostitos Cantina Traditional Yellow Corn Tortilla Chips because milk was not declared on the label. Affected products were distributed across 13 states.

    Product
    Tostitos Cantina Traditional Yellow Corn Tortilla Chips. Net Wt. 13oz. (368.5) UPC 0 28400-52848 1. Frito-Lay, Inc., Plano, TX 75024-4099.
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Food)·F-0677-2025·2025-04-09

    Choshiya Prepared Vegetables Recalled for Missing Refrigeration Label

    AKT Trading Inc. is recalling Choshiya branded Fukushin Zuke Prepared Mix Vegetables due to a labeling deficiency. The non-shelf-stable product is missing the required "Keep Refrigerated" statement.

    Product
    Choshiya branded "FUKUSHIN ZUKE PREPARED MIX VEGETABLES" UPC# JANCODE 4582207535142
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1498-2025·2025-04-09

    Anesthesia Circuit Kit Flex (P)2 recalled for potential breathing hose cracks

    Draeger, Inc. is recalling the Anesthesia Circuit Kit Flex (P)2 due to the potential for cracks to form in the breathing circuit hose. This FDA Class I recall affects approximately 9,250 units distributed domestically and internationally.

    Product
    Brand Name: Anesthesia Circuit Kit Product Name: Anesthesia Circuit Kit Flex (P)2 Model/Catalog Number: MP02752 Software Version: Not applicable Product Description: Accessory for conducting medical gases between anesthesia machine and patient for anesthetic use. Kit is inten
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·25E024000·2025-04-08

    ILJIN Hysolus Recalls Compressed Natural Gas Tanks Due to Rupture Risk

    ILJIN Hysolus is recalling specific CNG tanks because the pressure relief device may not fully vent, potentially causing the tank to rupture and increasing the risk of fire and injury.

    Product
    FUEL SYSTEM, OTHER:STORAGE:TANK ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·011-2025·2025-04-05

    Johnsonville Recalls Cheddar Bratwurst Due to Possible Hard Plastic Contamination

    Johnsonville is recalling approximately 22,672 pounds of cheddar bratwurst sold in ten states due to possible hard plastic contamination. No injuries have been reported.

    Product
    Momence Real Estate — Johnsonville, LLC, Recalls Cheddar Bratwurst Product Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    10 states
  • SevereCPSC·25208·2025-04-03

    Polaris RZR Pro R and Pro R 4 recalled for ROPS fastener defect

    Polaris is recalling about 910 RZR Pro R and Pro R 4 recreational off-road vehicles (2022-2025) due to missing or loose fasteners on the rollover protective structure that can fail to protect occupants in a rollover or tip-over.

    Product
    Model Year 2022-2025 RZR Pro R and RZR Pro R 4 Recreational Off-Road Vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·25204·2025-04-03

    USB-Powered LED Bear Lights Recalled for Fire and Burn Hazards

    Five Below is recalling about 29,000 LED Iridescent Bear Lights because the USB power switch can overheat and melt. The company received 28 reports of overheating, including 6 finger burns and 2 property damage incidents.

    Product
    Room2Room LED Iridescent Bear Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·25207·2025-04-03

    Honda Recalls Accessory Heaters for Side-by-Side Vehicles Due to Fire Hazards

    Honda is recalling about 2,340 aftermarket accessory heaters for Pioneer and Talon side-by-side vehicles because they can overheat and catch fire. The company has received three reports of overheating, including two that resulted in fires and vehicle damage.

    Product
    Accessory Heaters for Model Years 2022-2024 Honda Pioneer 1000, 2023-2025 Pioneer 700, and 2022-2024 Honda Talon 1000 Side-by-Side vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide