The Recall Desk

Severity 4 of 5

Severe recalls

The hazard poses a serious risk of illness, injury, or structural failure. 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 32222

  • SevereCPSC·26763·2026-09-10

    Triumph Recalls 2025-2026 TF450 Motorcycles Due to Engine Crash Hazard

    Triumph is recalling 2025 and 2026 TF450 closed-course competition motorcycles because a seized engine rocker arm can cause a crash, posing a risk of serious injury or death.

    Product
    2025 and 2026 Triumph TF450 models Closed Course Competition Motorcycles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26755·2026-09-10

    Prepared Hero Recalls Fire Spray Canisters Due to Rupture Risk

    Prepared Hero is recalling about 31,000 Hero Fire Spray Canisters because they may deteriorate and rupture during a fire, posing a risk of serious injury or death.

    Product
    Hero Fire Spray Canisters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V584000·2026-09-10

    Chrysler Recalls Jeep Wagoneer Models for Roof Rack Bolt Defect

    Chrysler is recalling specific Jeep Wagoneer and Grand Wagoneer models because improperly tightened roof rack bolts may allow crossbars to detach, creating a road hazard.

    Product
    JEEP — JEEP GRAND WAGONEER, WAGONEER, GRAND WAGONEER L, WAGONEER L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3086-2026·2026-09-09

    Fresenius 5008X HD/HDF Blood Tubing Set Recalled for Leak Risk

    Fresenius Medical Care is recalling 18,600 units of 5008X HD/HDF blood tubing sets due to a heightened probability of blood leaks that could cause blood loss and hypovolemia.

    Product
    5008X HD/HDF with CLiC Blood Tubing Set Part number 03-5300-3C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0819-2026·2026-09-09

    Baxter Recalls Vasopressin Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Vasopressin in 0.9% Sodium Chloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    VASOPRESSIN IN 0.9% SODIUM CHLORIDE — VASOPRESSIN IN 0.9% SODIUM CHLORIDE (VASOPRESSIN IN 0.9% SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1309-2026·2026-09-09

    Hampton Grocer Lactation Granola Recalled for Salmonella Contamination Risk

    The Hampton Grocer is recalling Small Batch Lactation Granola due to potential Salmonella contamination. Consumers should stop eating the product and return it for a refund.

    Product
    THE HAMPTON GROCER brand; Lacnola; SMALL BATCH LACTATION GRANOLA, 8oz, stand up pouches; NUTRIENT DENSE INGREDIENTS + MORINGA; SUPPORTS + PROMOTES HEALTHY LACTATION; INGREDIENTS Organic Gluten Free Oats Organic Maple Syrup Organic Pumpkin Seeds Organic Coconut Oil Almond Butter…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3085-2026·2026-09-09

    Fresenius 5008X Blood Tubing Set Recalled for Potential Blood Leak

    Fresenius Medical Care is recalling 5008X HD/HDF Standard Blood Tubing Sets due to a heightened probability of blood leak from the Arterial Alpha Clip connection.

    Product
    5008X HD/HDF Standard Blood Tubing Set Part Number 03-5300-3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3061-2026·2026-09-09

    Medline Eye and Cataract Kits Recalled for Potential Sterility Breach

    Medline is recalling 2,080 eye and cataract preop kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) EYE KIT, Model Number: DYKM2751; 2) EYE KIT, Model Number: DYKM2751A; 3) CATARACT PREOP KIT, Model Number: DYKS1583A; 4) CATARACT PREOP KIT, Model Number: DYKS1583B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3063-2026·2026-09-09

    Medline Blood Draw and Phlebotomy Kits Recalled for Sterility Breach

    Medline is recalling approximately 996,692 blood draw and phlebotomy kits due to potential sterility breaches in the packaging. The defect may expose patients to microbial contamination.

    Product
    Medline Convenience Kits: 1) BLOOD DRAW KIT, Catalog Number: DYLAB1081; 2) WHOLE BLOOD PHLEBOTOMY KIT, Catalog Number: DYNDB3005D; 3) QP KIT, Catalog Number: DYNDB3005F; 4) DOUBLE RED CELL PHLEBOTOMY KIT, Catalog Number: DYNDB3006C; 5) PLATELET PHLEBOTOMY KIT, Catalog…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V576000·2026-09-09

    Ford Recalls 2026 F-150s Due to Rear Axle Bearing Defect

    Ford is recalling 2026 F-150 vehicles because incorrect rear axle tail bearings may cause wheel lock-up or driveshaft separation, increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0809-2026·2026-09-09

    Baxter Recalls Famotidine Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Famotidine Injection due to CGMP deviations. The product was distributed in the US, Puerto Rico, and Chile.

    Product
    FAMOTIDINE — FAMOTIDINE (FAMOTIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1308-2026·2026-09-09

    Weis Pasteurized Apple Cider Recalled for High Patulin Levels

    Weis Markets is recalling Pasteurized Apple Cider in Pennsylvania due to high patulin levels. Consumers should stop using the product.

    Product
    Weis (Fresh From the Orchard ) Pasteurized Apple Cider, Contains 100 % Juice, the product comes in the following sizes: Pints, 1/2 Gallon, Gallon, plastic jug. 6 1/2 - gallon jugs per crate.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0810-2026·2026-09-09

    Baxter Recalls Dexmedetomidine Hydrochloride Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Dexmedetomidine Hydrochloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 400 mcg per 100 mL (4 mcg/mL) in Galaxy 100 mL Single Dose Container, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, USA, NDC 0338-9557-12.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0821-2026·2026-09-09

    Baxter Recalls Daptomycin Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Daptomycin Injection due to Current Good Manufacturing Practice (CGMP) deviations. The recall covers the US, Puerto Rico, and Chile.

    Product
    Daptomycin, in 0.9% Sodium Chloride Injection, 1,000 mg per 100 mL (10 mg/mL), 1,000 mg total, in 1000 mL Single Dose Container, Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-0718-12.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3084-2026·2026-09-09

    Fresenius Medical Care Recalls 5008X Standard HD Pre-Flush Blood Tubing Sets

    Fresenius Medical Care is recalling 120 units of 5008X Standard HD Pre-Flush Blood Tubing Sets due to a heightened probability of blood leaks during treatment.

    Product
    5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3062-2026·2026-09-09

    Medline Convenience Kits Recalled for Potential Sterility Breach

    Medline is recalling 18,290 convenience kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) ORTHO ASPIRATION KIT, Model Number: DYKM1636A; 2) SHOULD BLOCK KIT, Model Number: DYKM1881A; 3) TRIMA KIT, Model Number: DYNDB3077C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E063000·2026-09-09

    Ford Recalls Battery Energy Control Modules for Software Defect

    Ford is recalling specific Battery Energy Control Modules (BECM) because software errors may cause incorrect charge readings or overheating, increasing crash and fire risks.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY:MANAGEMENT SYSTEM/ENERGY CONTROL MODULE (BMS/BECM):SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1327-2026·2026-09-09

    Ukrop's Bread Pudding Recalled for Metal Fragments

    Ukrop's Homestyle Foods is recalling Bread Pudding with Vanilla Sauce kits due to potential metal fragments. The product was distributed in Kentucky, North Carolina, Virginia, and West Virginia.

    Product
    Bread Pudding with Vanilla Sauce - KIT NET WT 4 LB (1.81Kg) UPC 7 22515 91732 0 Ukrop's Homestyle Foods, LLC Richmond, VA 23230
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-3048-2026·2026-09-09

    Medline Convenience Kits Recalled for Potential Sterility Breach

    Medline is recalling 104 convenience kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) DRAWER 9 CRICOTHYROTOMY KIT, Model Number: ACC010741; 2) KIT ANESTHESIA L&D A- LINE SET, Model Number: DYKMBNDL199A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3057-2026·2026-09-09

    Medline Blood Culture Kits Recalled for Potential Sterility Breach

    Medline is recalling 3,650 blood culture kits nationwide due to potential packaging defects that may compromise sterility and expose patients to microbial contamination.

    Product
    Medline Convenience Kits: 1) BLOOD CULTURE TRAY PEDIATRIC, Model Number: DYNDH1193; 2) BLOOD CULTURE KIT 2 W/CONNECT, Model Number: DYNDH1487A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1329-2026·2026-09-09

    Fayus Inc. Recalls OLA-OLA Pounded Yam for Undeclared Milk

    Fayus Inc. is voluntarily recalling OLA-OLA Pounded Yam (Iyan) IYANINSTANT in multiple sizes due to undeclared milk. The product was distributed in six US states and two foreign countries.

    Product
    OLA-OLA Pounded Yam (Iyan) IYANINSTANT, NET WT. 2 lbs., 4 lbs., 5 lbs., 10 lbs, packed in flexible plastic bags. INGREDIENTS: Processed Dehydrated Yam Flour, freshness preserved by BHT & sodium bisulfite. UPCs: (2 lb): 650655244825, (4 lb): 650655496873, (5 lb): 650655244856…
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Drugs)·D-0817-2026·2026-09-09

    Baxter Recalls Clindamycin Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Clindamycin Injection due to CGMP deviations. The affected product was distributed in the US, Puerto Rico, and Chile.

    Product
    CLINDAMYCIN PHOSPHATE — CLINDAMYCIN PHOSPHATE (CLINDAMYCIN PHOSPHATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1319-2026·2026-09-09

    Savor Seasonings Recalls Organic Cheddar Seasoning for Undeclared Milk Allergen

    Savor Seasonings LLC is recalling Organic Cheddar Type Seasoning because it tested positive for undeclared milk. The product was distributed to one consignee in Canada.

    Product
    Organic Cheddar Type Seasoning, NET WT: 50 lbs. Product is packaged in bulk poly-lined paper bag. Savor Seasonings, LLC. 4292 Armstrong Boulevard Batavia, OH 45103. Product distribution: 218 (50-lb) bags + 2 partial bags (27-lb and 34-lb, one from each lot respectively).
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·26V583000·2026-09-09

    Daimler Trucks Recalls Freightliner and Western Star Trucks for Brake Defect

    Daimler Trucks North America is recalling certain 2020-2023 Freightliner Cascadia and 2022 Western Star 49X trucks because corroded brake valves may cause the vehicle to pull during braking.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR CASCADIA, 49X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·021-2026·2026-09-09

    El Eden Recalls Ineligible Pork Crackling Potato Chips from Colombia

    El Eden Import Distributor Corp. is recalling potato chips containing pork cracklings imported from Colombia because the country is ineligible to export meat to the U.S.

    Product
    El Eden Import Distributor Corp Recalls Ineligible Pork Cracklings Products Imported from The Republic of Colombia
    Category
    Food
    Distribution
    6 states