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.

1676–1700 of 29084

  • SevereFDA (Devices)·Z-1943-2025·2025-06-25

    Dexcom G6 Glucose Receiver recalled for missed audible alerts

    Dexcom G6 Glucose Receiver units may have defective foam or assembly errors that disable audible alerts for dangerously low or high blood glucose, risking seizures, loss of consciousness, or death.

    Product
    Dexcom G6 Glucose Receiver, SKUs (Part Number): STK-FM-001 (MT27408-1) & STK-FR-001 (MT27408-1)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0057-2025·2025-06-25

    Ginger Beer Juice Soda Recalled for Potential Salmonella Contamination

    RGB Soda, LLC is recalling Refrigerated Cucumber X Tarragon Ginger Beer distributed in Washington due to potential Salmonella contamination. The affected batches were produced on 11/4/2024 and 11/25/2024.

    Product
    Refrigerated Cucumber X Tarragon Ginger Beer (ginger juice). Product is juice soda and distributed in 5gal. pony keg. The kegs were distributed to the firm's own stores where they were served to glasses. The kegs were labeled with the name of the product and the day it was made.
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·25V414000·2025-06-25

    International CV brake pressure sensor can leak fluid causing fire

    International is recalling certain 2019-2025 CV vehicles because the brake pressure sensor assembly may leak brake fluid into the pressure switch and short circuit. Owners are advised to park outside until repaired.

    Product
    INTERNATIONAL — INTERNATIONAL CV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0938-2025·2025-06-25

    Afghani Corn Bread Doda Recalled for Undeclared Wheat and Sesame

    Ariana Sweets Inc. is recalling Afghani Corn Bread "Doda" because the product contains undeclared wheat and sesame allergens, which are not listed on the label.

    Product
    AFGHANI CORN BREAD "Doda"; INGREDIENTS: Corn Flour, Sugar, Vegetable Oil, Eggs, Milk, Black Seeds, Caardamom; ALLERGEN STATEMENT: This product contains eggs, milk, and may contain traces of nuts. NET WT 24.0 oz (680g); Keep Cool. Reheat in oven if desired.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0492-2025·2025-06-25

    UNAVY ACIDO HIALURONICO supplement recalled for undeclared pharmaceutical ingredients

    UNAVY ACIDO HIALURONICO hyaluronic acid supplement is being recalled because it contains three undeclared pharmaceutical ingredients: Dexamethasone, Diclofenac, and Omeprazole. The product was marketed without FDA approval and poses health risks from the unlisted drugs.

    Product
    UNAVY ACIDO HIALURONICO, Conenido: 30 capletas de 850mg, distribuido por: EREN NATURAL S.A. DE C.V, Zappan, Jal. C.P, UPC 7 503046 054295
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0054-2025·2025-06-25

    Ready-to-eat salads recalled for potential Salmonella contamination

    GBC Food Services is recalling multiple ready-to-eat salad products due to potential Salmonella contamination. The affected salads were purchased between May 8 and May 21, 2025.

    Product
    Chef Salad 11oz 850065403328 Purchase Dates: 05/08/2025 to 05/21/2025 Family Cobb Salad 22OZ 850054894625 Purchase Dates: 05/08/2025 to 05/21/2025 Individual Garden Salad 12OZ 850054894618 Purchase Dates: 05/08/2025 to 05/21/2025 Individual Greek Salad 12OZ 850054894649 Purchase
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Devices)·Z-1902-2025·2025-06-25

    Cook Beacon Tip Angiographic Catheters Recalled for Tip Separation Risk

    Cook Incorporated is recalling specific lots of Beacon Tip 5.0 Fr Angiographic catheters due to the risk that the catheter tip may separate during use. The affected catheters were distributed worldwide.

    Product
    Beacon Tip 5.0 Fr Angiographic catheters are designed to facilitate diagnostic and therapeutic procedures. Catheters are available in various configurations. Configurations include different shaft lengths and tip curves and some catheters are manufactured with a hydrophilic coati
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·25V380000·2025-06-23

    GEM Recalls 2022-2025 Electric Vehicles Due to Ball Joint Separation Risk

    GEM is recalling 2022-2025 e2, e4, e6, and eLXD vehicles because improperly tightened fasteners may cause the front lower ball joint to separate, potentially leading to a loss of steering control.

    Product
    GEM — GEM E4, E6, ELXD, E2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V425000·2025-06-20

    Travel trailer patio door transit latch cannot be opened from inside

    Forest River is recalling certain 2025-2026 Wildwood and Salem travel trailers because the exterior transit latch on the rear patio door cannot be unlocked from inside the vehicle.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V419000·2025-06-19

    Subaru Forester child seat anchor bolts may come loose

    Subaru is recalling certain 2025 Forester vehicles because the child seat anchor bolts may have been improperly tightened, allowing them to come loose.

    Product
    SUBARU — SUBARU FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V385000·2025-06-19

    Vanguard Recalls 2021-2023 VXP Trailers Due to Hook Box Defect

    Vanguard is recalling 2021-2023 VXP 28-Foot Pup trailers because the pintle hook box assembly may crack or break, reducing stability while being towed.

    Product
    VANGUARD — VANGUARD VXP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V422000·2025-06-19

    Honda Recalls 2013 Accord Vehicles for Driveshaft Corrosion Risk

    Honda is recalling 2013 Accord vehicles with 4-cylinder engines and CVTs in 23 states and D.C. because the driveshaft may corrode and break, potentially causing a loss of drive power or vehicle rollaway.

    Product
    HONDA — HONDA ACCORD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0033-2025·2025-06-18

    Jean's Classy Fresh Salsa Hot recalled due to Salmonella contamination

    TGD Cuts, LLC is recalling Jean's Classy Fresh Salsa, Hot (6/12 oz. plastic tubes) due to Salmonella contamination. The affected product was distributed to Maryland, Pennsylvania, North Carolina, Virginia, and New Jersey.

    Product
    Jean's Classy Fresh Salsa, Salsa, Hot 6/12 oz., Plastic tube, 6 per case .
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·25V413000·2025-06-18

    Mazda CX-50 airbag module software may cause improper deployment

    Mazda is recalling certain CX-50 Hybrid and CX-50 vehicles because incorrectly configured module software may cause the airbag to deploy improperly. All affected vehicles are under dealer control.

    Product
    MAZDA — MAZDA CX-50 HYBRID, CX-50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0037-2025·2025-06-18

    Cucumber Sliced Unpeeled 2 oz. Pack Recalled for Salmonella

    TGD Cuts, LLC is recalling Cucumber Sliced Unpeeled (Item #7065, UPC #840219170657) in 2 oz. packs due to Salmonella contamination. The product was distributed to Maryland, Pennsylvania, North Carolina, Virginia, and New Jersey.

    Product
    Cucumber Sliced Unpeeled, Pack Size 50, 2 oz. , 50 per case
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Food)·H-0028-2025·2025-06-18

    Cucumber 5lb Cases Recalled Due to Potential Salmonella Contamination

    Lipman Family Farms is recalling Cucumber 5lb cases distributed across 18 states due to potential Salmonella contamination. Consumers should not consume the product and should dispose of it or return it to the retailer.

    Product
    Cucumber 5lb Repacked by Lipman Produce Hendersonville, NC 28792, Product of USA
    Category
    Food
    Distribution
    18 states
  • SevereFDA (Food)·H-0031-2025·2025-06-18

    Smartcuts Cucumber Sliced Trays recalled due to Salmonella contamination

    Smartcuts Cucumber Sliced Trays 2/2lb have been recalled because they may be contaminated with Salmonella. Affected lots include F13625, F13825, and F14025 with expiration dates from 05/25 to 05/29.

    Product
    Smartcuts Cucumber Sliced Trays 2/2lb
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1867-2025·2025-06-18

    Z-800W Infusion System Recalled for Unvalidated Software Installation

    Zyno Medical LLC is recalling the Z-800W Infusion System because unreleased software versions were installed on devices without verification or validation.

    Product
    Z-800W Infusion System. Intended to provide intravenous infusion of parenteral fluids, blood, and blood products to a patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1972-2025·2025-06-18

    BD Texium Closed System Drug Transfer Devices May Leak at Connector

    BD Texium closed system drug transfer devices in multiple sizes may leak at the interface between the male luer component and needle-free connector, potentially causing treatment delays, exposure to hazardous drugs, and underdosing.

    Product
    BD Texium: 3 mL, REF: MY8003-0006; 5 mL, REF: MY8005-0006; 10 mL, REF: MY8010-0006; 20 mL, REF: MY8020-0006; 30 mL, REF: MY8030-0006; 60 mL, REF: MY8060-0006
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0464-2025·2025-06-18

    MALEXTRA Dietary Supplement Recalled for Undeclared Pharmaceutical Ingredients

    MALEXTRA Recharge with Extra dietary supplement is being recalled nationwide because laboratory testing found undeclared pharmaceutical ingredients propoxyphenylsildenafil and sildenafil in the product.

    Product
    MALEXTRA, Recharge with Extra, Dietary Supplement, 10 capsules per box, Distributed by: Health Fixer, Tempe, AZ 85288, UPC B0CWKZ6ZP3.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0097-2025·2025-06-18

    Non Fat Dry Milk Recalled for Potential Salmonella Contamination

    Crystal Creamery Inc. is recalling non fat dry milk due to potential Salmonella contamination. The affected product was distributed in California and Texas.

    Product
    NON FAT DRY MILK. "LOW HEAT SPRAY PROCESS GRADE A NON FAT DRY MILK MADE FROM PASTERUIZED MILK, NET WEIGHT 25.00 KG, PRODUCT OF U.S.A."
    Category
    Food
    Distribution
    2 states
  • SevereCPSC·25351·2025-06-18

    MaxKare Electric Blankets Recalled for Burn and Fire Hazards

    MaxKare electric blankets (model HB18A) sold on Walmart.com can overheat and catch fire, posing burn hazards. Yumo has received 34 reports of overheating, including 3 burn injuries and 2 fires.

    Product
    MaxKare Electric Blankets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1953-2025·2025-06-18

    Tecfen Medical 20G MVR Sideport Knife ophthalmic sterility recall

    Tecfen Medical is recalling its 20G (1.2mm) MVR Sideport Knife Straight (Model QKN2312) ophthalmic knives due to sterility assurance concerns. The recall affects 38 units distributed in the US and internationally.

    Product
    Brand Name: Tecfen Medical Product Name: 20G (1.2mm) MVR Sideport Knife Straight Model/Catalog Number: QKN2312 Software Version: No software Product Description: This is an ophthalmic knife (manual( that is to be sterile and packaged individually in Tyvek 1059B. MVR sideport
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1932-2025·2025-06-18

    Philips Intera 1.5T Explorer/Nova Dual MRI Gradient Coil Fire Risk

    Philips is recalling one Intera 1.5T Explorer/Nova Dual MRI system due to a gradient coil component that may overheat, produce smoke, or ignite, risking patient and operator injury.

    Product
    Intera 1.5T Explorer/Nova Dual Product Number: 781108;
    Category
    Medical Device
    Distribution
    Distributed nationwide