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 the agency’s own highest classification or reported deaths or serious injuries, 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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526–550 of 7451

  • CriticalFDA (Devices)·Z-2656-2025·2025-10-08

    MAGNETOM Cima.X systems recalled over ice blockage in helium venting system

    Siemens is recalling 22 MAGNETOM Cima.X (DE) systems because an ice blockage in the magnet venting system could prevent helium escaping during a quench.

    Product
    MAGNETOM Cima.X (DE). Model Number: 11647158.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2667-2025·2025-10-08

    MAGNETOM Vida MRI systems recalled over ice blockage in magnet venting

    Siemens is recalling 498 MAGNETOM Vida (DE) MRI systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.

    Product
    MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213805, K220425, K231560.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2665-2025·2025-10-08

    MAGNETOM Verio Dot systems recalled over magnet venting ice blockage risk

    Siemens is recalling 59 MAGNETOM Verio Dot systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.

    Product
    MAGNETOM Verio Dot. Model Number: 10684333.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2662-2025·2025-10-08

    MAGNETOM Skyra Fit BioMatrix systems recalled over magnet vent ice blockage

    Siemens is recalling 39 MAGNETOM Skyra Fit BioMatrix systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.

    Product
    MAGNETOM Skyra Fit BioMatrix. Model Number: 11516217.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2610-2025·2025-10-08

    Reprocessed steerable electrophysiology catheters recalled over residual particulates on surfaces

    Medline is recalling 7,913 reprocessed Livewire Steerable Electrophysiology Catheters because specific lots may carry small residual particulates on patient-contacting surfaces.

    Product
    Reprocessed Livewire Steerable Electrophysiology Catheter Item Numbers 401575RH 401582RH 401600RH 401603RH 401606RH 401652RH 401653RH 401654RH 401904RH 401905RH 401908RH 401914RH 401915RH 401918RH 401932RH 401933RH 401934RH 401938RH 401939RH 401940RH…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2668-2025·2025-10-08

    MAGNETOM Vida Fit MRI systems recalled over magnet vent ice blockage

    Siemens is recalling 41 MAGNETOM Vida Fit MRI systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.

    Product
    MAGNETOM Vida Fit. Model Number: 11410481.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2659-2025·2025-10-08

    MAGNETOM Prisma MRI systems recalled over helium venting ice blockage

    Siemens is recalling 101 MAGNETOM Prisma MRI systems because an ice blockage in the magnet venting system could prevent helium escaping during a quench.

    Product
    MAGNETOM Prisma. Model Number: 10849582.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·031-2025·2025-10-04

    Foster Poultry Farms Recalls Chicken Corn Dogs and Ground Turkey Sticks

    Foster Poultry Farms is recalling chicken corn dogs and ground turkey on a stick products due to possible wood contamination. Consumers should not eat these items.

    Product
    Foster Poultry Farms, LLC — Foster Poultry Farms, LLC Recalls Chicken Corn Dog and Ground Turkey on a Stick Products Due To Possible Extraneous Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0632-2025·2025-10-01

    Monterey jack and provolone loaves recalled over potential Listeria monocytogenes contamination

    Middlefield Original Cheese Co-op Monterey Jack and Provolone 5 lb loaves with a sell-by date of 2/13/2026 are recalled for potential Listeria monocytogenes contamination. 7,455 lbs are affected.

    Product
    1) Middlefield Original Cheese Co-op Monterey Jack, 5 lb., packaged as loaves wrapped in plastic and packed 8 loaves per case 2) Middlefield Original Cheese Co-op Provolone, 5 lb., packaged as loaves wrapped in plastic and packed 2 loaves per case
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Devices)·Z-2566-2025·2025-10-01

    Intubation trays recalled after laryngoscope handle lights failed to illuminate

    Medline is recalling 2,520 intubation and airway kits containing Flexicare BritePro Solo fiber optic laryngoscope handles because the light may fail to illuminate as intended.

    Product
    Medline medical convenience kits labeled as: 1. ADULT INTUBATION TRAY, Kit Number ACC010369B; 2. ADULT ICU INTUBATION TRAY, Kit Number ACC010379A; 3. INTUBATION TRAY, Kit Number ACC010392; 4. INTUBATION KIT, Kit Number ACC010467A; 5. ADULT AIRWAY TRAY, Kit Number…
    Category
    Medical Device
    Distribution
    6 states
  • CriticalFDA (Food)·H-0627-2025·2025-10-01

    Shredded mozzarella and provolone recalled over potential Listeria monocytogenes contamination

    Middlefield Original Cheese Co-op Shredded Mozzarella/Provolone Cheese, 5 lb bags with a sell-by date of 9/3/2025, is recalled for potential Listeria monocytogenes contamination. 7,455 lbs are affected.

    Product
    Middlefield Original Cheese Co-op Shredded Mozzarella/Provolone Cheese, 5 lbs., packaged in a plastic bag, packed 4 bags per case
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·H-0630-2025·2025-10-01

    Original Swiss cheese recalled over potential Listeria monocytogenes contamination

    Middlefield Original Cheese Co-op Original Swiss Cheese, in 5 lb loaves and 2 lb deli bags with a sell-by date of 2/13/2026, is recalled for potential Listeria monocytogenes contamination.

    Product
    Middlefield Original Cheese Co-op Original Swiss Cheese, packaged as 5 lb. loaves wrapped in plastic and packed 2 loaves per case (distribution) or 8 loaves per case (retail), or sliced and packaged as 2 lb. deli bags and packed 5 bags per case
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·H-0633-2025·2025-10-01

    Shredded mozzarella cheese recalled over potential Listeria monocytogenes contamination

    Middlefield Original Cheese Co-op Shredded Mozzarella Cheese, 5 lb bags with a sell-by date of 9/3/2025, is recalled for potential Listeria monocytogenes contamination.

    Product
    Middlefield Original Cheese Co-op Shredded Mozzarella Cheese, 5 lb., shredded in a plastic bag and packed 4 bags per case
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·H-0028-2026·2025-10-01

    Macaroni and cheese cartons recalled nationwide for undeclared cashew allergen

    GOODLES is recalling 61,176 cartons of Here Comes Truffle creamy truffle flavored cheddar and shells because the product contains cashews that are not declared on the label.

    Product
    GOODLES HERE COMES TRUFFLE CREAMY TRUFFLE FLAVORED CHEDDAR AND SHELLS NET WT 6 OZ (170g) INGREDIENTS: GOODLES SHELLS (WHEAT FLOUR, CHICKPEA PROTEIN, WHEAT PROTEIN, NUTRIENTS EXTRACTED FROM [BROCCOLI, SPINACH, KALE, PUMPKIN, SWEET POTATO, SUNFLOWER SEED, CRANBERRY, CHLORELLA…
    Category
    Food
    Distribution
    37 states
  • CriticalFDA (Food)·H-0027-2026·2025-10-01

    Plant-based white cheddar spirals recalled over undeclared milk allergen

    GOODLES Vegan Is Believin' Plant-Based White Cheddar with Spirals, 5.25 oz, is recalled for undeclared milk. The FDA classified the action as Class I. 129,660 cartons are affected.

    Product
    GOODLES VEGAN IS BELIEVIN' PLANT-BASED WHITE CHEDDAR WITH SPIRALS NET WT 5.25 OZ (149g) INGREDIENTS: GOODLES SPIRALS (WHEAT FLOUR, CHICKPEA PROTEIN, WHEAT PROTEIN, NUTRIENTS EXTRACTED FROM [BROCCOLI, SPINACH, KALE, PUMPKIN, SWEET POTATO, SUNFLOWER SEED, CRANBERRY, CHLORELLA…
    Category
    Food
    Distribution
    37 states
  • CriticalFDA (Food)·H-0626-2025·2025-10-01

    Organic gouda cheese recalled over potential Listeria monocytogenes contamination

    Middlefield Original Cheese Co-op Organic Gouda Cheese, 8 oz, with a sell-by date of 2/13/2026, is recalled for potential Listeria monocytogenes contamination.

    Product
    Middlefield Original Cheese Co-op Organic Gouda Cheese, 8 oz., packaged individually in plastic, packed 12 per case
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Food)·H-0631-2025·2025-10-01

    Pepper jack cheese loaves recalled over potential Listeria monocytogenes contamination

    Middlefield Original Cheese Co-op All Natural Pepper Jack Cheese, in 5 lb loaves and 2 lb deli bags, is recalled for potential Listeria monocytogenes contamination. The FDA classified the action as Class I.

    Product
    1) Middlefield Original Cheese Co-op All Natural Pepper Jack Cheese, packaged as 5 lb. loaves wrapped in plastic and packed 2 loaves per case (distribution) or 8 loaves per case (retail), or sliced and packaged as 2 lb. deli bags and packed 5 bags per case 2) Middlefield…
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Devices)·Z-2538-2025·2025-09-24

    Wheelchair power assist speed dials recalled over potential loss of control

    SmartDrive MX2+ SpeedControl Dials are recalled because a faulty electrical connection between the dial and the wheelchair motor may cause loss of control. The FDA classified the action as Class I. 25,389 units are affected.

    Product
    Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.
    Category
    Medical Device
    Distribution
    52 states
  • CriticalFDA (Food)·H-0608-2025·2025-09-24

    Sliced peeled cucumbers in 10 lb boxes recalled over Salmonella contamination

    Cucumber Sliced PLD KBS in 2/10 lb cardboard boxes, code X3234937, is recalled because the product is contaminated with Salmonella. The FDA classified the action as Class I.

    Product
    Cucumber Sliced PLD ¿ KBS 2/10lb, Cardboard Boxes
    Category
    Food
    Distribution
    4 states
  • CriticalFDA (Devices)·Z-2540-2025·2025-09-24

    SmartDrive speed control dials recalled over faulty motor electrical connection

    SmartDrive MX2+ SpeedControl Dials, REF MX2-3DCMC, are recalled because a faulty electrical connection between the dial and the wheelchair motor may cause loss of control. 8,413 units are affected.

    Product
    Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCMC use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.
    Category
    Medical Device
    Distribution
    52 states
  • CriticalFDA (Food)·H-0612-2025·2025-09-24

    Spanish club ciabatta sandwiches recalled over undeclared wheat and milk

    Spanish Club Ciabatta, 10.5 oz, from Fresh and Ready Foods is recalled for undeclared wheat and milk. The FDA classified the action as Class I. 233 units are affected.

    Product
    Spanish Club Ciabatta; Keep Refrigerated, NET WT: 10.5 OZ, UPC# 6 82906 90933 7 Manufactured by Fresh and Ready Foods LLC, San Fernando, CA 91340
    Category
    Food
    Distribution
    1 state