The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

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.

4476–4500 of 52939

  • HighNHTSA·25V333000·2025-05-21

    Mack Recalls 2026 MD Trucks Due to Incorrect Seat Belt Routing

    Mack Trucks is recalling 2026 MD vehicles because the center bench seat belt assembly may be routed incorrectly, potentially failing to restrain occupants in a crash.

    Product
    MACK — MACK MD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1749-2025·2025-05-21

    Abbott Alinity m Resp-4-Plex AMP Kit Multiplex PCR Test Recall

    Abbott Molecular is recalling the Alinity m Resp-4-Plex AMP Kit (List Number 09N79-096) due to reports of increased reactive negative controls and false positive results in respiratory viral testing.

    Product
    Alinity m Resp-4-Plex AMP Kit, List Number 09N79-096, a multiplex real-time reverse transcription (RT) polymerase chain reaction (PCR) test intended for the simultaneous qualitative detection and differentiation of RNA from SARS-CoV-2, influenza A virus (flu A), influenza B virus
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1743-2025·2025-05-21

    Halyard RAPIDES E-PACK Cardiovascular Procedure Kit Surgical Needle Coating Issue

    AVID Medical is recalling Halyard RAPIDES E-PACK Cardiovascular Procedure Convenience Kits due to a raw material defect in surgical needle coating that may cause diminished performance or coating removal during use.

    Product
    Halyard RAPIDES E-PACK. Cardiovascular Procedure Convenience Kit.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0767-2025·2025-05-21

    Bonya Peach Yogurt Parfait recalled for undeclared almonds

    Knockroe Inc is recalling Bonya Peach Yogurt Parfait (8oz cups) distributed to NY, PA, MA, and NJ due to undeclared almonds that may pose a risk to consumers with tree nut allergies.

    Product
    Bonya Peach Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0766-2025·2025-05-21

    Bonya Mango Yogurt Parfait recalled for undeclared almonds

    Knockroe Inc is recalling Bonya Mango Yogurt Parfait (8oz) because it contains undeclared almonds, a major food allergen. The product was distributed to NY, PA, MA, and NJ.

    Product
    Bonya Mango Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1769-2025·2025-05-21

    KliniTray Platte Faxitron Sterile Tissue Resection Examination Board Recalled

    KliniTray Platte Faxitron sterile tissue resection margin examination boards (Model 2001155-F) are being recalled due to potential for microbial contamination. Affected units were distributed nationwide.

    Product
    KliniTray Platte Faxitron ,groB "R" sterile. Tissue resection margin examination board/large Model Number: 2001155-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization of alignment during surgical procedures. It ensures the exact
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0765-2025·2025-05-21

    Bonya Blueberry Yogurt Parfait recalled for undeclared almonds

    Knockroe Inc is recalling Bonya Blueberry Yogurt Parfait (8 oz) distributed in NY, PA, MA, and NJ because the product contains undeclared almonds, which poses a risk to consumers with tree nut allergies.

    Product
    Bonya Blueberry Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1768-2025·2025-05-21

    KliniTray surgical alignment system recalled for microbial contamination risk

    Klinika Medical is recalling the KliniTray tissue resection margin examination board (Model 2001105-F) due to potential microbial contamination. The device was distributed nationwide in Massachusetts.

    Product
    KliniTray. KlinioTray. Tissue resection margin examination board/small. Model Number: 2001105-F The medical device KliniTrayTM is a system for the precise monitoring, recording and visualization of alignment during surgical procedures. It ensures the exact orientation and posi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1770-2025·2025-05-21

    Philips Enterprise 1.5T MRI Equipment Quadrature Body Coil Seal

    Philips is recalling Enterprise 1.5T MRI scanners (Model 781145) because the Quadrature Body Coil seal adhesive may fail, creating sharp edges that could injure patients during scanning.

    Product
    Enterprise 1.5T, Model Number: 781145;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·25E036000·2025-05-21

    Holley Recalls Fuel Pressure Regulators Due to Leak Risk

    Holley Performance Products is recalling specific Fuel Pressure Regulators because a damaged diaphragm may cause a fuel leak, increasing the risk of fire.

    Product
    FUEL SYSTEM, GASOLINE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1748-2025·2025-05-21

    Abbott Alinity m Resp-4-Plex Amplification Kit Recall

    Abbott Molecular is recalling the Alinity m Resp-4-Plex Amplification Kit due to reports of reactive negative controls and false positive results in respiratory virus testing.

    Product
    Alinity m Resp-4-Plex Amplification (AMP) Kit (CE), List Number 09N79-090, a multiplex real-time reverse transcription (RT) polymerase chain reaction (PCR) test intended for the qualitative detection and differentiation of RNA from influenza A virus (flu A), influenza B virus (fl
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1774-2025·2025-05-21

    Philips Intera 1.5T MRI Quadrature Body Coil seal adhesive failure

    Philips is recalling Intera 1.5T MRI systems due to potential failure of the Quadrature Body Coil seal adhesive, which may create sharp edges and contact patient skin during scanning.

    Product
    Intera 1.5T, Model Numbers: 781195 and 781295;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0777-2025·2025-05-21

    Kasundi Peeled Mango Pickle in Oil recalled for elevated lead levels

    Advance Food International Inc. is recalling Kasundi Peeled Mango Pickle in Oil due to elevated lead levels detected in the product. The affected product was distributed in the Northeast.

    Product
    National brand Kasundi PEELED MANGO PICKLE IN OIL; Net Wt.: 1 Kg (35.27 oz)/ 2.20lb; Ingredients: Kasundi (Peeled Mango), Canola Oil, Cabbage, Salt, Mixed Spices, Vinegar, Sodium Benzoate as preservative; Product of Pakistan; packaged in a plastic jar with a red lid
    Category
    Food
    Distribution
    6 states
  • HighFDA (Food)·F-0808-2025·2025-05-21

    Dixit Foods Sabudana Khichadi Recalled for Undeclared Milk and Peanut Allergens

    Dixit Foods Sabudana Khichadi (200 g) is recalled due to undeclared milk and/or peanut allergens. The product may pose a serious risk to consumers with allergies to these ingredients.

    Product
    Dixit Foods, Sabudana Khichadi, Net Wt. 200 g, Ingredients: Sago (Sabudana), Crushed Groundnuts, Sugar, DesiGhee, Salt, Green Chilli, Cumin Seeds. Allergen Information: May contain Peanuts, Treenuts, Wheat, Sesame, Mustard
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-0801-2025·2025-05-21

    New England Village Snacks Mix Recalled for Undeclared Allergens

    New England Village Snacks The 19th Hole Snack Mix (5 oz. and 10 oz.) is being recalled due to undeclared almonds and sesame. Consumers with allergies to these ingredients should not consume the product.

    Product
    New England Village Snacks The 19th Hole Snack Mix (5 oz. and 10 oz.)
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1771-2025·2025-05-21

    Philips Intera 0.5T Standard MRI System Quadrature Body Coil Seal

    Philips is recalling the Intera 0.5T Standard MRI system (Model 781101) because the Quadrature Body Coil seal adhesive may fail and create sharp edges that could injure patients during scanning.

    Product
    Intera 0.5T Standard, Model Number: 781101;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0781-2025·2025-05-21

    Wells Dairy Peanut Butter N Fudge Ice Cream Recall Plastic Foreign Material

    Wells Enterprises is recalling Peanut Butter 'N Fudge Ice Cream 3-gallon tubs because plastic foreign material may be present in the product.

    Product
    Peanut Butter 'N Fudge Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640050574, Item: 33429
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0764-2025·2025-05-21

    Bonya Vanilla Yogurt Parfait recalled for undeclared almonds

    Knockroe Inc is recalling Bonya Vanilla Yogurt Parfait (8oz) due to undeclared almonds, which pose a risk to consumers with almond allergies. The product was distributed to NY, PA, MA, and NJ.

    Product
    Bonya Vanilla Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-1762-2025·2025-05-21

    Tornado Embolization Microcoil recalled for incorrectly sized coils

    Cook Incorporated is recalling Tornado Embolization Microcoils due to incorrectly sized coils in affected lots. The devices are used for vascular embolization procedures.

    Product
    Tornado Embolization Microcoil, intended for embolization of selective vessel supply to arteriovenous malformations and other vascular lesions, RPN MWCE-18S-3/2-TORNADO (GPN G08261), RPN MWCE-18S-3/2-TORNADO-081800 (GPN G13102), RPN MWCE-18S-4/2-TORNADO (GPN G08357)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0790-2025·2025-05-21

    Vanilla Frozen Yogurt Recalled for Possible Plastic Foreign Material

    Wells Enterprises is recalling Vanilla Frozen Yogurt 3-gallon tubs due to the possible presence of plastic material in the product.

    Product
    Vanilla Frozen Yogurt, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 00070640022144, Item: 1352604
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0786-2025·2025-05-21

    Quick Blend Vanilla Flavored Ice Cream recalled for plastic contamination

    Wells Enterprises is recalling Quick Blend Vanilla Flavored Ice Cream (3-gallon tubs) because plastic material may be present in the product.

    Product
    Quick Blend Vanilla Flavored Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640050604, Item: 773034
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0792-2025·2025-05-21

    Wells Dairy GFGB Vanilla Ice Cream Recalled for Plastic Contamination

    Wells Enterprises is recalling GFGB 12% Vanilla Flavored Ice Cream (3-gallon tubs) because plastic foreign material may be present in the product. Consumers should not consume the product and should contact the company or retailer.

    Product
    GFGB 12% Vanilla Flavored Ice Cream, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640018451, Item: 1435313
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0800-2025·2025-05-21

    Ellington Farms Vanilla Flavored Ice Cream Recalled for Plastic

    Wells Enterprises, Inc. is recalling Ellington Farms Vanilla Flavored Ice Cream (3-gallon tubs) distributed across the US because plastic material may be present in the product.

    Product
    Ellington Farms Vanilla Flavored Ice Cream, 3 GAL, DISTRIBUTED BY Ben E. Keith Foods, Fort Worth, TX 76101 UPC: 046045065833, Item: 1144464
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0787-2025·2025-05-21

    Planet Smoothie Frozen Yogurt Recalled for Possible Plastic Foreign Material

    Wells Enterprises is recalling Planet Smoothie ZSA Vanilla Flavored Fat Free Frozen Yogurt (3-gallon tubs) because plastic foreign material may be present in the product.

    Product
    Planet Smoothie ZSA Vanilla Flavored Fat Free Frozen Yogurt, 3 GAL, Wells Enterprises, INC dba Wells Dairy, Inc Le Mars, IA 51031, UPC: 070640005567, Item: 889334
    Category
    Food
    Distribution
    0 states
  • HighFDA (Food)·F-0771-2025·2025-05-21

    Bonya Coconut Yogurt Parfait Recalled for Undeclared Almonds

    Knockroe Inc is recalling Bonya Coconut Yogurt Parfait (8 oz) distributed to NY, PA, MA, and NJ because it contains undeclared almonds, a common allergen.

    Product
    Bonya Coconut Yogurt Parfait, 8oz, Plastic cups with plastic inserts for granola, 6 units per case for distributors, 12 units per case for all other customers, Always Refrigerate .
    Category
    Food
    Distribution
    4 states