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.

5101–5125 of 29102

  • SevereFDA (Food)·F-0828-2023·2023-05-17

    Revolution Farms Salad Kits Recalled for Listeria Contamination

    Revolution Farms is recalling Traverse City Cherry 6-ounce salad kits due to potential Listeria monocytogenes contamination. Affected products were distributed in Michigan, Ohio, and Wisconsin.

    Product
    Revolution Farms Traverse City Cherry 6oz salad kit in plastic container UPC 856791008226
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0876-2023·2023-05-17

    FDA Recalls Kimura Burdock Salt for Undeclared Fish Allergen

    Daiso California Warehouse is recalling Kimura burdock salt because it contains fish (sardines, bonito, tuna) not listed on the label. People with fish allergies may have a serious allergic reaction.

    Product
    Kimura burdock salt 40g UPC: 4972304293524
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0823-2023·2023-05-17

    Revolution Farms Green Sweet Crisp Recalled for Listeria monocytogenes

    Revolution Farms is recalling Green Sweet Crisp and Sweet Crisp Deli Leaf products from Michigan, Ohio, and Wisconsin due to potential Listeria monocytogenes contamination. Consumers should not eat and should discard affected products.

    Product
    Revolution Farms Green Sweet Crisp plastic 5oz Retail container UPC 856791008141 and 3lb bulk clear poly bag UPC 856791008172 Revolution Farms Sweet Crisp Deli Leaf plastic 5oz Retail container UPC 856791008189
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1486-2023·2023-05-17

    Emboli Capture Guidewire System Recalled Due to Potential Component Separation

    Cordis US Corp recalls 54 units of the ANGIOGUARD RX/XP Emboli Capture Guidewire System due to potential separation of device components. This could delay procedures or result in unplanned intervention, including possible stroke.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 701814RMC
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0832-2023·2023-05-17

    Meijer Chicken Cobb Salad Recalled Due to Listeria Contamination Risk

    Meijer Inc. is recalling Fresh From Meijer Chicken Cobb Salad due to potential Listeria monocytogenes contamination. The product was distributed to Meijer stores in six states.

    Product
    Fresh From Meijer Chicken Cobb Salad 8.8 Oz UPC - 719283679321
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-1488-2023·2023-05-17

    FDA Class I Guidewire System Recalled for Device Separation Risk

    Cordis US Corp is recalling the ANGIOGUARD RX / XP Emboli Capture Guidewire System because the device may separate during procedures, risking stroke or requiring emergency intervention.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 603014MC
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1483-2023·2023-05-17

    ANGIOGUARD RX / XP Emboli Capture Guidewire System separation during procedures

    The ANGIOGUARD RX / XP emboli capture guidewire system may separate from its delivery sheath during medical procedures, potentially leading to stroke or complications requiring emergency intervention.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RMC
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0836-2023·2023-05-17

    Fresh From Meijer Shareable Garden Salad Recalled for Listeria

    Fresh From Meijer Shareable Garden Salad 11.5 oz is being recalled due to potential Listeria monocytogenes contamination. The recall affects salads distributed to Meijer stores across six states with a sell-by date of 3/31/2023.

    Product
    Fresh From Meijer Shareable Garden Salad 11.5 Oz UPC - 713733295376
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-1492-2023·2023-05-17

    ANGIOGUARD Emboli Capture Guidewire System Recalled Due to Device Separation

    The FDA has recalled the ANGIOGUARD RX/XP Emboli Capture Guidewire System because the delivery system and capture sheath could separate during use, potentially causing stroke or requiring emergency surgery.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RE
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·23V349000·2023-05-17

    Foretravel Recalls 2022-2024 Motorhomes Due to Software Error

    Foretravel is recalling 2022-2024 Realm, FS450, and Realm Presidential motorhomes because a software error may cause loss of drive power or disable safety systems.

    Product
    FORETRAVEL — FORETRAVEL REALM, REALM PRESIDENTIAL, FS450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0841-2023·2023-05-17

    Vitamin B Capsules Recalled for Undeclared Milk Allergen

    EuroMedica and Terry Naturally vitamin B complex capsules are being recalled nationwide due to undeclared milk allergen. Consumers with milk allergies should not use these products.

    Product
    Multiple Vitamin B Capsules, 60 Capsules, Biologically Active Forms of Vitamin B12, Folate, B6. Packaged in bottles under the following brands: 1. EuroMedica Active B Complex, Product #68006, UPC 3 67703 68006 0. Manufactured by a cGMP compliant facility exclusively for: Eur
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0835-2023·2023-05-17

    Meijer Mediterranean Salad Recalled Due to Listeria Contamination

    Meijer Inc is recalling Fresh From Meijer Mediterranean Salad due to potential Listeria monocytogenes contamination. Approximately 1,064 units were distributed to Meijer stores in six Midwest states.

    Product
    Fresh From Meijer Mediterranean Salad - 6.5 Oz UPC - 713733246132
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-1489-2023·2023-05-17

    Emboli Capture Guidewire System recalls risk of device separation during procedures

    Cordis is recalling an emboli capture guidewire system due to potential separation of components during medical procedures. The separation could cause procedural delays, unplanned interventions, or stroke.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814REC
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0829-2023·2023-05-17

    Revolution Farms Salad Kit Recalled for Listeria Contamination

    Revolution Farms Zesty Southwest salad kits are being recalled due to potential Listeria monocytogenes contamination. Affected products were distributed in Michigan, Ohio, and Wisconsin.

    Product
    Revolution Farms Zesty Southwest 6oz salad kit in plastic container UPC 856791008240
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1485-2023·2023-05-17

    ANGIOGUARD RX/XP Guidewire System May Separate During Medical Procedures

    The ANGIOGUARD RX/XP Emboli Capture Guidewire System may separate during medical procedures, potentially delaying treatment or requiring unplanned intervention. The recall affects 471 units distributed worldwide.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RMC
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-0827-2023·2023-05-17

    Revolution Farms Sesame Ginger Crunch Salad Kit Recalled for Listeria Monocytogenes

    Revolution Farms Sesame Ginger Crunch 6oz salad kits (UPC 856791008233, 'Sell By 3/23/23') are recalled due to potential Listeria monocytogenes contamination. Affected units were distributed in Michigan, Ohio, and Wisconsin.

    Product
    Revolution Farms Sesame Ginger Crunch 6oz salad kit in plastic container UPC 856791008233
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-1491-2023·2023-05-17

    Emboli Capture Guidewire System recalled due to potential device separation

    Cordis US Corp is recalling the ANGIOGUARD RX/XP Emboli Capture Guidewire System (1,087 units worldwide) due to potential separation of the delivery system and capture sheath, which could lead to stroke.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RE
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1428-2023·2023-05-17

    Cook Blue Rhino G2 Tracheostomy Introducer Trays Recalled for Connection Defect

    Cook Incorporated is recalling Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Trays because the device connectors are not making secure connections with 15mm caps and other circuit components, resulting in unsecure connections.

    Product
    Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Tray, Reference Part Numbers C-PTISYJ-100-HC-G-EU-FLEX8.5 (G57725), C-PTISYJ-100-HC-G-NA-FLEX7.5 (G57720), C-PTISYJ-100-HC-G-NA-FLEX8.5 (G57721), C-PTISY-100-HC-G-NA-FLEX8.5 (G57717), C-PTISY-100-HC-G-NA-FLEX7.5 (G57716)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0824-2023·2023-05-17

    Revolution Farms Romaine Lettuce Recalled for Listeria Contamination

    Revolution Farms romaine lettuce products distributed in Michigan, Ohio, and Wisconsin are recalled due to potential Listeria monocytogenes contamination. Consumers should not consume affected products and should discard them.

    Product
    Revolution Farms Robust Romaine plastic 5oz Retail container UPC 856791008035 and 3lb bulk clear poly bag UPC 856791008127 Revolution Farms Romaine Lettuce Boats plastic 5oz Retail container UPC 856791008196 Revolution Farms Whole Leaf Romaine plastic 5oz Retail container UPC
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0831-2023·2023-05-17

    Meijer Chicken Caesar Salads Recalled Due to Listeria monocytogenes Contamination

    Meijer Inc. is recalling Fresh From Meijer Chicken Caesar Salads (6.4 oz and 10 oz sizes) due to potential Listeria monocytogenes contamination. Products were distributed to Meijer stores in six states: Michigan, Indiana, Illinois, Ohio, Kentucky, and Wisconsin.

    Product
    Fresh From Meijer Chicken Caesar Salad 6.4 Oz UPC - 760236117452 Fresh From Meijer Chicken Caesar Shareable Salad 10 Oz UPC - 719283679338
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0871-2023·2023-05-17

    Takuma Herb Salt Peanuts Recalled for Undeclared Fish Allergen

    Daiso California Warehouse is recalling Takuma food herb salt peanuts because the product contains fish (Bonito, Sardines, Tuna) but does not list it on the label. Consumers with fish allergies could unknowingly consume the product.

    Product
    Takuma food herb salt peanut 80g UPC: 4962679652767
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Food)·F-0840-2023·2023-05-17

    Salad Product Recalled by Meijer for Listeria Contamination

    Meijer Inc is recalling Fresh From Meijer Cranberry Spinach Shareable Salad due to potential Listeria monocytogenes contamination. The product was distributed to Meijer stores in Michigan, Indiana, Illinois, Ohio, Kentucky, and Wisconsin.

    Product
    Fresh From Meijer Cranberry Spinach Shareable Salad 12 Oz UPC - 708820304321
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-1494-2023·2023-05-17

    Emboli Capture Guidewire System recalled for component separation risk

    The ANGIOGUARD RX/XP Emboli Capture Guidewire System is being recalled because the delivery system and capture sheath may separate during procedures, potentially causing stroke or requiring emergency surgical intervention.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RM
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Drugs)·D-0567-2023·2023-05-17

    Atovaquone Oral Suspension Recalled for Bacillus cereus Contamination

    Camber Pharmaceuticals is recalling Atovaquone Oral Suspension due to contamination by Bacillus cereus bacteria. The contamination was discovered during testing of repackaged medication.

    Product
    ATOVAQUONE — ATOVAQUONE (ATOVAQUONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1495-2023·2023-05-17

    Emboli Capture Guidewire System Separation Risk Recalls ANGIOGUARD RX/XP

    Cordis US Corp is recalling ANGIOGUARD RX/XP Emboli Capture Guidewire Systems worldwide due to potential separation of the delivery system and capture sheath during procedures, which could cause stroke or require emergency intervention.

    Product
    ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 501814RM
    Category
    Medical Device
    Distribution
    0 states