The Recall Desk

Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means deaths or serious injuries are reported, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

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4601–4625 of 36541

  • SevereFDA (Devices)·Z-0594-2024·2024-01-10

    Tracheostomy care sets recalled for sterility assurance failure

    Busse Hospital Disposables is recalling tracheostomy care kits due to failed sterility assurance. The affected product cannot guarantee required sterility levels and poses risks of infection and sepsis.

    Product
    Catalog No. 9251R1, 9251R2, 9251R3 TRACHEOSTOMY CARE SET / STERILE - LATEX FREE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0690-2024·2024-01-10

    Soy Bean Sprouts Recalled Due to Listeria Contamination

    Samsung Bean Sprout is recalling Sung Soy Bean Sprouts (1lb packages) distributed to Virginia due to Listeria monocytogenes contamination. Products have a sell-by date of 12/14/23.

    Product
    Sung Soy Bean Sprouts, 1lb packages, in plastic packages, 20 bags per case
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0591-2024·2024-01-10

    Omnipod 5 insulin pump app bolus calculator decimal point error

    The Omnipod 5 app bolus calculator may fail to record a decimal point if entered first when adjusting a dose, potentially causing insulin over-delivery. Users should verify dose values on both the calculator and confirmation screens before administering insulin.

    Product
    Omnipod 5 App (on compatible Android smartphones), Software Versions 1.1 - 1.2.3 (current). US: PT-000599- Omnipod 5 App Software Package (provided through Google Play), EU: PT-001323- Omnipod 5 App Software Package (provided on locked-down Controllers (PT-001194 and PT-001193).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0596-2024·2024-01-10

    Regard Dressing Change Kit Recalled Due to Defective Irrigation Solution

    ROi CPS LLC is recalling Regard Dressing change kits (Item 800026006) due to a defective irrigation solution component. Approximately 1,830 units distributed in Louisiana are affected.

    Product
    Regard Dressing change kit, Item Number 800026006
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V008000·2024-01-09

    PL Custom Recalls 2020-2024 Ambulances Due to Electrical Fire Risk

    PL Custom is recalling 2020-2024 Type 1 and Type 3 ambulances because a firmware defect may cause electrical circuits to overheat and catch fire.

    Product
    PL CUSTOM — PL CUSTOM TYPE III, TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V006000·2024-01-08

    E-One Recalls Fire Trucks Due to Electrical Fire Risk

    E-One is recalling 408 fire trucks because a wiring defect may cause electrical circuits to overheat and start a fire.

    Product
    E-ONE — E-ONE TYPHOON N, COMMERCIAL, CYCLONE E, CYCLONE N
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V003000·2024-01-05

    Forest River Recalls 2020 Cherokee Travel Trailers Due to Draw Bar Defect

    Forest River is recalling 2020 Cherokee travel trailers because the draw bar locking mechanism may break, causing the trailer front to contact the road and increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·002-2024·2024-01-05

    Salm Partners Recalls Turkey Kielbasa Due to Bone Fragments

    Salm Partners, LLC is recalling ready-to-eat turkey kielbasa products due to possible contamination with bone fragments.

    Product
    Salm Partners, LLC — Salm Partners, LLC Recalls Ready-to-Eat Turkey Kielbasa Products Due to Possible Extraneous Material Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V002000·2024-01-04

    Terex Advance Concrete Mixer Trucks Recalled for Drum Separation Risk

    Terex Advance is recalling 2023-2024 concrete mixer trucks because bolts may loosen, causing the drum to separate from the vehicle.

    Product
    TEREX ADVANCE — TEREX ADVANCE COMMANDER, MM300, CHARGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0600-2024·2024-01-03

    Megadyne Patient Return Electrode Recalled Due to Serious Burn Injury Reports

    Megadyne Medical Products is recalling the MEGA SOFT Universal Plus Patient Return Electrode due to reports of serious burn injuries, including third-degree burns. The device should not be used in patients under 12 years old.

    Product
    Product Code 0848, MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode, Reusable Patient Return Electrode, Mega Soft Universal Dual Plus
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·001-2024·2024-01-03

    Busseto Foods Recalls Charcuterie Meat Due to Salmonella Risk

    Fratelli Beretta USA is recalling Busseto Foods charcuterie samplers due to possible Salmonella contamination linked to a multistate outbreak investigation.

    Product
    Fratelli Beretta USA, Inc. — Fratelli Beretta USA, Inc. Recalls Busseto Foods Brand Ready-to-Eat Charcuterie Meat Products Due to Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0599-2024·2024-01-03

    Megadyne MEGA SOFT Return Electrode Recalled for Serious Burn Injuries

    Megadyne Medical Products is recalling approximately 2,312 MEGA SOFT Universal Plus Patient Return Electrodes due to reports of serious patient burn injuries, including third-degree burns. The product is now restricted to patients age 12 and older.

    Product
    Product Code 0847, MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode, Reusable Patient Return Electrode, Mega Soft Universal Plus
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0597-2024·2024-01-03

    MEGADYNE MEGA SOFT Return Electrode Recalled Due to Reported Patient Burn Injuries

    Megadyne Medical Products is recalling its MEGA SOFT Universal Patient Return Electrode due to reports of patient burn injuries, including third-degree burns requiring intervention. The product is now limited to use in patients age 12 and older.

    Product
    Product Code 0845, MEGADYNE MEGA SOFT Universal Patient Return Electrode, Reusable Patient Return Electrode
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0209-2024·2024-01-03

    Sure Regular Antiperspirant Deodorant Aerosol Recalled for Benzene Contamination

    Sure Regular Antiperspirant Deodorant Aerosol (6 oz cans) sold nationwide in the US and Canada is being recalled due to benzene contamination. All lots expiring on or before August 2023 are affected.

    Product
    Sure Regular Antiperspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%), packaged in 6 oz (170 g) aerosol cans, Distributed by Idelle Labs, Ltd., El Paso, TX 79912, NDC 41595-5518-06
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0563-2024·2024-01-03

    Medline Nurse Training Kits Recalled for Sharp Tracheostomy Brush

    Medline Industries recalls 550 educational nurse training kits due to sharp edges on tracheostomy brush components that can puncture tubing or cause injury, and bristles that may detach during or before use.

    Product
    (1) Nurse Kit, SKU #EDUC1025, Case UPC 40195327196647, Non-sterile, For Training Purposes Only, Not For Human Use.; and (2) Nursing Tote Kit, SKU #EDUC5056A, Case UPC 40195327153695, Non-sterile, For Training Purposes Only, Not For Human Use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0598-2024·2024-01-03

    Megadyne Patient Return Electrodes Recalled Due to Serious Burn Risk

    Megadyne Medical Products recalls its MEGA SOFT Universal Dual Patient Return Electrode due to reports of severe burn injuries, including third-degree burns requiring medical intervention. Use is now restricted to patients age 12 and older.

    Product
    Product Code 0846, MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode, Reusable Patient Return Electrode, Mega Soft Universal Dual Cord
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0562-2024·2024-01-03

    Medline Nursing Skills Kit: Tracheostomy Brush Sharp Edge and Bristle Defect

    Medline is recalling 172 Nursing Skills kits due to defects in the tracheostomy brush component. The brush has a sharp edge that can puncture tubing and cause user injury, and bristles may detach during use.

    Product
    (1) Nursing Skills kit, SKU #EDUC05038B, Case UPC 40195327019878, Non-sterile, For Training Purposes Only, Not For Human Use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0561-2024·2024-01-03

    Medline Tracheostomy Care Kits Recalled for Sharp Brush and Bristle Detachment

    Medline is recalling 620,735 tracheostomy care kits because the brush component has a sharp edge that can puncture tubing and injure users, and bristles can detach during use.

    Product
    Tracheostomy care kits: (1) Medline Tracheostomy Clean and Care Tray with 14 Fr Suction Catheter, REF DYND40580, Sterile; (2) Medline Tracheostomy Clean and Care Tray, REF DYND4061030, Sterile; (3) Medline Basic Tracheostomy Care Kit, REF CC3T4691A, Sterile; (4) Medli
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0206-2024·2024-01-03

    Supplement Capsules Recalled for Undeclared Sildenafil Content Nationwide

    Magnum XXL 9800 capsules contain undeclared sildenafil and were marketed without FDA approval. The product was distributed nationwide via Amazon.

    Product
    Magnum XXL 9800, 2000 mg per capsule, 1 capsule per blister pack, Distributed by Magnum Los Angelas CA. UPC 6 45759 99300 7. Amazon's ASIN# B07P7ZH797, B07P94J3ZT, B07P6VK6N3, B076HNPZZZ
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0207-2024·2024-01-03

    Brut Classic Antiperspirant and Deodorant Recalled for Benzene Contamination

    Brut Classic Antiperspirant & Deodorant in 4 oz and 6 oz aerosol cans is being recalled due to benzene contamination. The recall affects all lots distributed in the United States and Canada.

    Product
    Brut Classic Antiperspirant & Deodorant (aluminum chlorohydrate 20.9%) packaged in a) 4 oz. (113g) aerosol cans (UPC 00827755070085, NDC 41595-7103-1) and b) 6 oz. (170g) aerosol cans (UPC 00827755070108, NDC 41595-7103-2), Distributed by Idelle Labs, Ltd. El Paso, TX 79912 USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E001000·2024-01-03

    Spektrum Brakes Recalls Dynamic Friction R1 Brake Rotors Due to Fracture Risk

    Spektrum Brakes is recalling Dynamic Friction R1 brake rotors because the hub can fracture, causing a loss of braking ability and increasing crash risk.

    Product
    SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:DISC:ROTOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0208-2024·2024-01-03

    Sure Unscented Deodorant Aerosol Recalled for Benzene Contamination

    Sure Unscented Deodorant Aerosol is being recalled nationwide due to benzene contamination. Consumers should stop using affected cans and contact the manufacturer.

    Product
    Sure Unscented Anti-perspirant Deodorant Aerosol (Aluminum Chlorohydrate 10%), packaged in 6 oz (170 g) aerosol cans, Distributed by Idelle Labs, Ltd., El Paso, TX 79912, NDC 41595-5517-06
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V903000·2023-12-29

    2023–2024 INEOS Grenadier vehicles recalled for faulty steering fasteners

    Ineos Automotive Americas is recalling certain 2023–2024 Grenadier vehicles due to non-locking nuts that may have been installed on the steering rod ball joint, risking steering failure and loss of vehicle control.

    Product
    INEOS — INEOS GRENADIER QUARTERMASTER, GRENADIER
    Category
    Vehicle
    Distribution
    Distributed nationwide