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.

376–400 of 6113

  • SevereFDA (Food)·H-0491-2026·2026-02-18

    Kirkland Signature mini beignets recalled for undeclared hazelnut

    Costco is recalling Kirkland Signature Mini Beignets (item #1181272) because they contain undeclared hazelnut, a common allergen. Approximately 8,073 packages were distributed across 24 US states.

    Product
    Kirkland Signature Costco item #1181272 Mini Beignets filled with Caramel 22CT. UPC 000011 812722. Product is packaged in a clear clamshell container. ALLERGENS INFORMATION: CONTAINS WHEAT, EGG, MILK, SOY. Distributed by Costco Wholesale Corp. PO Box 34535 Seattle, WA.
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0353-2026·2026-02-18

    Injectable drug recalled for temperature abuse during storage

    UDENYCA (pegfilgrastim-cbqv) injection is being recalled because 116 cartons of Lot 2199821 were stored at room temperature instead of required refrigerated conditions.

    Product
    UDENYCA — UDENYCA (PEGFILGRASTIM-CBQV)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1319-2026·2026-02-18

    Medline Reprocessed Cardiac Catheters Recalled for Particle Contamination Risk

    Medline reprocessed cardiac catheters may contain residual material particles, risking systemic infection, blood clots, and embolism. Affected units should be immediately quarantined and returned.

    Product
    Medline ReNewal Reprocessed Webster CS Catheters: Webster CS Catheter 10 Electrodes 2-8-2mm Spacing w/AutoID w/ EZ Steer BD710DF282CRH; Webster CS Catheter 10 Electrodes, 2-8-2mm Spacing w/ EZ Steer BD710DF282RRH BD710FJ282RRH; Webster CS Catheter 10 Electrodes, 2-8-2mm S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1323-2026·2026-02-18

    Medline Reprocessed ICE Catheters Recalled for Residual Material

    Medline Industries is recalling 650 units of ReNewal Reprocessed ViewFlex Xtra ICE Catheters due to contamination with residual material particles. These defective devices pose a risk of serious infection and life-threatening blood clots.

    Product
    Medline ReNewal Reprocessed ViewFlex Xtra ICE Catheters: ViewFlex Xtra ICE Catheter 9F x 90cm D087031RH 20197344019554¿
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0459-2026·2026-02-11

    Sofit Seedless Red Dates Recalled for Undeclared Sulfites

    Tai Phat Wholesalers, LLC is recalling Sofit Seedless Red Dates due to undeclared sulfites, an allergen. The 12 oz packages were distributed to Florida, Georgia, Iowa, and North Carolina.

    Product
    Sofit, Seedless Red Dates, 12 oz package, Plastic bags, 50 packages per case
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·H-0455-2026·2026-02-11

    JUICE from the Raw Cashew Milk Recalled for Potential Pathogenic Bacteria

    Everpress Juice is recalling JUICE from the Raw, a cashew milk product, due to potential pathogenic bacteria from under-processing. The product was distributed across multiple U.S. states.

    Product
    JUICE from the Raw, cashew milk
    Category
    Food
    Distribution
    24 states
  • SevereFDA (Food)·H-0460-2026·2026-02-11

    Organic Chia Seeds from Paraguay Recalled for Potential Salmonella

    Tradin Organics USA, LLC is recalling Organic Chia Seed Black from Paraguay due to potential Salmonella contamination. Product was distributed in California, Colorado, New York, and Canada.

    Product
    Organic Chia Seed Black Origin: PARAGUAY Net weight: 55.12 LBS Produced for: Tradin Organics USA, LLC, Aptos
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·H-0450-2026·2026-02-11

    JUICE from the Raw DETOX GREENS Recalled for Pathogenic Bacteria

    Everpress Juice is recalling JUICE from the Raw DETOX GREENS due to under-processing that may allow pathogenic bacteria to be present. The affected product was distributed across 23 states.

    Product
    JUICE from the Raw, DETOX GREENS
    Category
    Food
    Distribution
    24 states
  • SevereNHTSA·25V789000·2026-02-11

    2022 Lincoln Corsair PHEV battery defect recall increases crash and fire risk

    Ford is recalling certain Lincoln Corsair and Ford Escape plug-in hybrid vehicles (model years 2020-2024) due to a high-voltage battery defect that may cause loss of drive power or fire. Owners should use Auto EV mode and limit battery charge until a remedy is available.

    Product
    LINCOLN — 2022 LINCOLN CORSAIR PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0332-2026·2026-02-11

    Rheumacare Capsules Recalled Due to Lead Contamination

    Rheumacare capsules (30-count bottles) are being recalled due to lead contamination discovered during manufacturing. The affected product was distributed to one customer in New York and should not be used.

    Product
    Rheumacare capsules, 30 count bottle, Mfg in India by: Virgo UAP Pharma Pvt. Ltd., Ahmedabad, India UPC 8 904218 700313
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Devices)·Z-1161-2026·2026-02-11

    HOT AXIOS Stent Deployment and Expansion Issues FDA Class I Recall

    Boston Scientific is recalling 266 units of the HOT AXIOS Stent due to deployment and expansion issues that may require additional surgical intervention to remove the stent and close the puncture site.

    Product
    HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 6mm x 8mm; Material Number (UPN): M00553520;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1158-2026·2026-02-11

    AXIOS Stent Deployment System Recalled Due to Deployment and Expansion Failures

    Boston Scientific is recalling the AXIOS Stent and Electrocautery-Enhanced Delivery System (20mm x 10mm) due to reports of stent deployment and expansion failures that may require additional surgical or endoscopic intervention.

    Product
    AXIOS Stent and Electrocautery-Enhanced Delivery System - 20mm x 10mm; Material Number (UPN): M00553660;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1163-2026·2026-02-11

    Boston Scientific AXIOS Stent Deployment and Expansion Issues Recall

    Boston Scientific is recalling 588 units of HOT AXIOS biliary stents worldwide due to reports of deployment and expansion failures that may require additional endoscopic or surgical intervention.

    Product
    *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 20mm x 10mm; Material Number (UPN): M00553560;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1159-2026·2026-02-11

    Boston Scientific AXIOS Stent Deployment and Expansion Failure Recall

    Boston Scientific is recalling AXIOS stents due to reported deployment and expansion issues. The devices may fail to expand properly during procedures, potentially requiring additional surgical intervention.

    Product
    AXIOS Stent and Electrocautery-Enhanced Delivery System - 6mm x 8mm; Material Number (UPN): M00553680;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1162-2026·2026-02-11

    HOT AXIOS stent delivery system recalled due to deployment and expansion issues

    Boston Scientific recalls HOT AXIOS 8mm stent delivery system for deployment and expansion failures. The devices may require surgical intervention to remove the stent and close puncture sites.

    Product
    *HOT AXIOS Stent and Electrocautery-Enhanced Delivery System 8mm x 8mm; Material Number (UPN): M00553530;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1160-2026·2026-02-11

    AXIOS Stent Deployment and Expansion Failures Require Device Exchange or Removal

    FDA Class I recall of AXIOS Stents due to reported deployment and expansion failures. Affected patients may require device exchange or additional surgical intervention to remove the stent and close the puncture site.

    Product
    AXIOS Stent and Electrocautery-Enhanced Delivery System - 8mm x 8mm; Material Number (UPN): M00553690;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0481-2026·2026-02-11

    Bread Crumbs Recalled for Undeclared Egg and Milk Allergens

    Outside The Breadbox bread crumbs are being recalled due to undeclared egg and milk allergens. The recall affects 4,497 units distributed across eight states.

    Product
    Bread Crumbs, Outside The Breadbox brand, net wt. 8 oz, UPC 873799001554. Product is packaged in a clear stand up pouch. Intended use baking. Condition/Shelf Life shelf stable, 180 days. Firm name Outside The Breadbox, 2027 W Colorado Ave. Colorado Springs, CO.
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·H-0500-2026·2026-02-11

    Bread and Roll Mix Recalled for Undeclared Milk Allergen

    B.C. Williams Bakery Service is recalling Bread and Roll Mix sold nationwide due to undeclared milk allergen. Consumers with milk allergies could have serious allergic reactions if they consume this product.

    Product
    Bread and Roll Mix; 50 lb. multi-wall, kraft, poly-lined moisture proof bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0499-2026·2026-02-11

    Spice Cake Mix Recalled Due to Undeclared Milk Allergen

    B.C. Williams Bakery Service, Inc is recalling its spice cake mix in 50 lb. bags due to undeclared milk allergen. The product was distributed nationwide under Batch 221.

    Product
    Spice Cake Mix; 50 lb. multi-wall, kraft, poly-lined moisture proof bags
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0451-2026·2026-02-11

    Sweet greens juice recalled for potential pathogenic bacteria

    Everpress Juice is recalling its JUICE from the Raw sweet greens product due to potential pathogenic bacterial contamination. The product was distributed to 22 states.

    Product
    JUICE from the Raw, sweet greens
    Category
    Food
    Distribution
    24 states
  • SevereNHTSA·24V717000·2026-02-09

    2025 Brinkley RV Model Z Travel Trailer Safety Chain Recall

    Brinkley is recalling certain 2025 Model Z travel trailers with underrated safety chains. The chains can break, allowing the trailer to detach and increasing the risk of a crash.

    Product
    BRINKLEY RV — 2025 BRINKLEY RV MODEL Z
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V640000·2026-02-08

    2024 Toyota Sequoia Hybrid Tow Hitch Cover May Detach from Bumper

    Toyota is recalling 2024 and 2023 Sequoia Hybrid vehicles with tow hitch covers that may detach from the rear bumper. Detached covers can become road hazards and increase crash risk.

    Product
    TOYOTA — 2024 TOYOTA SEQUOIA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V561000·2026-02-07

    2024 Hyundai Santa Fe air bag wiring defect recall

    Hyundai is recalling 49,719 2024 Santa Fe and Santa Fe HEV vehicles due to a defective main floor wiring harness that can chafe and damage the air bag system, potentially causing unintended deployment or failure to deploy in a crash.

    Product
    HYUNDAI — 2024 HYUNDAI SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide