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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11051–11075 of 36632

  • SevereFDA (Devices)·Z-2573-2020·2020-07-22

    CME BodyGuard Microset Infusion Sets Recalled for Delivery Inaccuracy

    CME America is recalling BodyGuard Microset infusion sets because they may deliver therapy at inaccurate rates, potentially causing over-infusion or under-infusion.

    Product
    BodyGuard Microset, REF: A100-163XE90S
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Food)·F-1053-2020·2020-07-22

    Fresh Express Cole Slaw Recalled Due to Cyclospora Risk

    Fresh Express America's Fresh Old Fashioned Cole Slaw is recalled due to a possible health risk from Cyclospora. Consumers should check for specific product codes and dates.

    Product
    Fresh Express America's Fresh Old Fashioned Cole Slaw" 14oz, UPC 071279123011, Green cabbage & carrots
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1141-2020·2020-07-22

    Fresh Express Organic Sesame Asian Salad Kit Recalled for Cyclospora Risk

    Fresh Express is recalling Wholesome Pantry Organic Sesame Asian Salad Kits due to a possible health risk from Cyclospora. Consumers should not eat the product.

    Product
    Wholesome Pantry Organic Sesame Asian Salad Kit 13 oz., UPC 041190066292, Organic green cabbage, organic romaine Lettuce, organic radicchio, organic carrots & organic green onions
    Category
    Food
    Distribution
    32 states
  • SevereNHTSA·20V422000·2020-07-22

    Kia Recalls 2020 Stinger Vehicles for Steering Locking Defect

    Kia is recalling 2020 Stinger vehicles with 2.0L Turbo-GDI engines because a steering component may be defective, potentially causing the steering to lock or become difficult while driving.

    Product
    KIA — KIA STINGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2564-2020·2020-07-22

    CME BodyGuard Microset Infusion Sets Recalled for Delivery Inaccuracy

    CME America is recalling BodyGuard Microset infusion sets due to delivery inaccuracies that may cause over- or under-infusion of therapy.

    Product
    BodyGuard Microset with Filter, REF: A100-163XESF
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Food)·F-1138-2020·2020-07-22

    Fresh Express Signature Farms Green & Crisp Salad Recalled for Cyclospora Risk

    Fresh Express is recalling Signature Farms Green & Crisp salads due to a possible health risk from Cyclospora. Consumers should check their refrigerators for the affected product.

    Product
    Signature Farms Green & Crisp 11 oz., UPC 021130419128, Iceberg Lettuce, Romaine, red cabbage and carrots
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-2565-2020·2020-07-22

    CME America BodyGuard Microset Infusion Sets Recalled for Delivery Inaccuracy

    CME America is recalling BodyGuard Microset infusion administration sets because they may deliver therapy with significant inaccuracy, potentially causing over-infusion or under-infusion.

    Product
    BodyGuard Microset, REF: A120-161XPSV
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2586-2020·2020-07-22

    CME America Recalls CMExpress Microbore Sets Due to Delivery Inaccuracy

    CME America is recalling 13,280 CMExpress Microbore Sets because they may deliver fluids with significant inaccuracy, potentially causing over- or under-infusion of therapy.

    Product
    CMExpress Microbore Set, REF: A120-160C
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Food)·F-1133-2020·2020-07-22

    Fresh Express Marketside Shredded Iceberg Lettuce Recalled for Cyclospora Risk

    Fresh Express is recalling Marketside Shredded Iceberg Lettuce due to a possible health risk from Cyclospora. Consumers should check their refrigerators for affected products.

    Product
    Marketside Shredded Iceberg Lettuce 8 oz., UPC 681131328968, Iceberg lettuce
    Category
    Food
    Distribution
    32 states
  • SevereUSDA FSIS·015-2020 ·2020-07-17

    Hafiz Foods Recalls Chicken Samosas Lacking Federal Inspection

    Hafiz Foods is recalling approximately 675 pounds of frozen chicken samosas because the poultry was produced without federal inspection. No adverse reactions have been reported.

    Product
    Tempura Foods & Spices LLC — Hafiz Foods, Inc. Recalls Samosas Containing Chicken Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    5 states
  • SevereNHTSA·20V414000·2020-07-17

    Ford Recalls Lincoln MKX and Nautilus for Air Bag Wire Damage Risk

    Ford is recalling 2016-2020 Lincoln vehicles because seat tilt functions may damage air bag wiring, causing unintended deployment or failure to deploy.

    Product
    LINCOLN — LINCOLN MKX, NAUTILUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V415000·2020-07-17

    Ford Recalls 2020 Escape and Transit Vehicles for Air Bag Defect

    Ford is recalling 2020 Escape and Transit vehicles because a defective air bag component may prevent proper inflation during a crash, increasing injury risk.

    Product
    FORD — FORD ESCAPE, TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2504-2020·2020-07-15

    CTL Medical Recalls CEZANNE II TLIF Bullet-Tip Cages Due to Fracturing

    CTL Medical Corporation is recalling 46 units of CEZANNE II TLIF Bullet-Tip Cages because reports indicate the devices fractured during insertion.

    Product
    CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L30, H8mm, Part #018.1908.
    Category
    Medical Device
    Distribution
    9 states
  • SevereNHTSA·20V407000·2020-07-15

    Blue Bird Transit Bus Recall for Missing Seat Belt Hardware

    Blue Bird is recalling 2019-2021 Vision and All-American buses because seat belt anchorages may lack reinforcing washers, increasing injury risk in crashes.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN TRANSIT BUS, ALL AMERICAN, VISION, VISION TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2501-2020·2020-07-15

    CTL Medical Recalls CEZANNE II TLIF Bullet-Tip Cage Due to Fracturing

    CTL Medical Corporation is recalling 39 units of CEZANNE II TLIF Bullet-Tip Cage because reports indicate the device fractured during insertion.

    Product
    CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L26, H7mm, Part #018.1307.
    Category
    Medical Device
    Distribution
    9 states
  • SevereFDA (Devices)·Z-2489-2020·2020-07-15

    Prodimed Combicath Catheters Recalled for Sterility Assurance Concerns

    Prodimed Plastimed Division is recalling 300 Combicath catheters nationwide due to a lack of assurance of sterility.

    Product
    Prodimed Combicath catheters for blind or fibrescope-guided protected distal bronchial sampling (PDBS)- COMBICATH 90 cm x 1.9 mm Product Code: 58229 19US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2502-2020·2020-07-15

    CTL Medical Recalls CEZANNE II TLIF Bullet-Tip Cage Due to Fracture Reports

    CTL Medical Corporation is recalling 39 units of CEZANNE II TLIF Bullet-Tip Cages because reports indicate the devices fractured during insertion.

    Product
    CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L30, H7mm, Part #018.1907.
    Category
    Medical Device
    Distribution
    9 states
  • SevereFDA (Devices)·Z-2503-2020·2020-07-15

    CTL Medical Recalls CEZANNE II TLIF Bullet-Tip Cage Due to Fracturing

    CTL Medical Corporation is recalling 45 units of CEZANNE II TLIF Bullet-Tip Cages because reports indicate the devices fractured during insertion.

    Product
    CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L26, H8mm, Part #018.1308.
    Category
    Medical Device
    Distribution
    9 states
  • SevereFDA (Devices)·Z-2491-2020·2020-07-15

    Prodimed Combicath Paediatric Catheters Recalled Due to Sterility Assurance Issues

    Prodimed Plastimed Division is recalling 180 units of Combicath Paediatric catheters nationwide because the company cannot assure the sterility of the devices.

    Product
    Prodimed Combicath Paediatric catheters for blind protected distal bronchial sampling- COMBICATH 35 cm x 1.9 mm Product Code: 58 223 19US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1379-2020·2020-07-15

    EMD Serono Recalls Cetrotide Vials Due to Missing Rubber Stoppers

    EMD Serono is recalling 30,756 vials of Cetrotide because missing rubber stoppers could compromise sterility assurance.

    Product
    CETROTIDE — CETROTIDE (CETRORELIX ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V409000·2020-07-15

    Blue Bird Recalls School Buses Due to Seat Belt Anchor Defect

    Blue Bird is recalling 2018-2021 All-American and 2019-2021 Vision school buses because seat belt anchorages may lack reinforcing washers, increasing injury risk in crashes.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, ALL AMERICAN SCHOOL BUS, VISION SCHOOL BUS, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V406000·2020-07-14

    Setra Motorcoaches Recalled for Electronic Stability Control Defect

    Daimler Coaches North America is recalling 2018-2020 Setra motorcoaches because the Electronic Stability Control system can be disabled at unsafe speeds, increasing crash risk.

    Product
    SETRA — SETRA S417 TC, S407 CC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E048000·2020-07-13

    Curt Rambler RV Towbars Recalled for Axial Pivot Pin Failure Risk

    Curt Manufacturing is recalling Rambler RV Towbars because the axial pivot pin may loosen or fail, potentially causing the hitch to separate and increasing crash risk.

    Product
    TRAILER HITCHES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V400000·2020-07-10

    Forest River Recalls 2021 Riverstone Trailers Due to Wiring Defect

    Forest River is recalling specific 2021 Riverstone trailers equipped with an optional generator prep package due to incorrect transfer switch wiring that may cause voltage back feed.

    Product
    FOREST RIVER — FOREST RIVER RIVERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide