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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10976–11000 of 36632

  • SevereFDA (Devices)·Z-2660-2020·2020-07-29

    Becton Dickinson Recalls PowerLoc MAX Infusion Sets Due to Tubing Cracks

    Becton Dickinson is recalling PowerLoc MAX infusion sets because tubing cracks may cause leakage of chemicals or biohazard materials.

    Product
    PowerLoc MAX Power Injectable Infusion Set AllPoints Port Access System; Catalog Numbers AN132075 (UDI 00801741118968), AN142010 (UDI 00801741119231), AN142010G (UDI 00801741119323), AN142075 (UDI 00801741119224)
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2664-2020·2020-07-29

    Becton Dickinson Recalls SafeStep Huber Needle Sets Due to Tubing Cracks

    Becton Dickinson is recalling SafeStep Huber Needle Sets because tubing may crack or break, risking leakage of chemicals or blood.

    Product
    SafeStep Huber Needle Set AllPoints Port Access System; Catalog Numbers AN152075 (UDI 00801741119484), AN152075G (UDI 00801741119583), AN162010 (UDI 00801741119682), AN162010G (UDI 00801741119446), AN162075 (UDI 00801741119675), AN162075G (UDI 00801741119439)
    Category
    Medical Device
    Distribution
    0 states
  • CriticalCPSC·20157·2020-07-28

    Triangle Tube Recalls Prestige Gas Boilers Due to Carbon Monoxide Risk

    Triangle Tube is recalling about 63,000 Prestige Solo and Excellence gas boilers because a vent adapter may detach, causing carbon monoxide leaks. One death was reported.

    Product
    Prestige Solo & Prestige Excellence condensing gas boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V432000·2020-07-28

    High Altitude Trailer XT50 Recalled for Rear Swing Arm Weld Failure

    High Altitude Trailer is recalling 2019-2020 XT50 trailers with retrofitted rear swing arm spare tire carriers because a weld may fail, causing the tire to separate and increasing crash risk.

    Product
    HIGH ALTITUDE TRAILER — HIGH ALTITUDE TRAILER XT50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E051000·2020-07-28

    Meritor Recalls P220 and P579 Pressure Assemblies Due to Hose Fitting Defect

    Meritor is recalling specific pressure assemblies where an incorrect fitting may cause the power steering hydraulic hose to fail, resulting in a loss of steering assist.

    Product
    STEERING:HYDRAULIC POWER ASSIST:HOSE, PIPING, AND CONNECTIONS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V435000·2020-07-28

    Daimler Recalls 2021 Thomas Built Buses Saf-T-Liner C2 School Buses

    Daimler Trucks North America is recalling 2021 Saf-T-Liner C2 School Buses because the brake pedal arm may rotate out of position, increasing crash risk.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V434000·2020-07-28

    BMW Recalls 2019-2020 X5 and X6 M for Steering Column Defect

    BMW is recalling 2019-2020 X5 and 2020 X6 M vehicles because the steering column shaft bearing plate may not be properly attached, which can affect handling and increase crash risk.

    Product
    BMW — BMW X5, X6 M
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·017-2020·2020-07-28

    Jamaican Tastee Patties Recalls Meat and Poultry Products Lacking Federal Inspection

    Jamaican Tastee Patties, LLC is recalling approximately 60,457 pounds of beef and chicken patty products that were repackaged and relabeled without federal inspection.

    Product
    Jamaican Tastee Patties, LLC Recalls Meat and Poultry Patty Products Produced without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·20V430000·2020-07-24

    Mercedes-Benz Recalls One 2020 GLE 350 for Seat Bolt Issue

    Mercedes-Benz is recalling one 2020 GLE 350 because a driver's seat bolt may not be installed correctly, which could increase injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V429000·2020-07-24

    Peterbilt 520 Recall: Steering Assist Bracket Bolts May Loosen

    PACCAR is recalling 2020 Peterbilt 520 trucks because incorrect bolts may allow the steering assist bracket to loosen, potentially locking the steering.

    Product
    PETERBILT — PETERBILT 520
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·016-2020·2020-07-24

    Coco's Italian Market Recalls Frozen Meat Products Produced Without Inspection

    Coco's Italian Market is recalling approximately 16,868 pounds of frozen meat products produced without federal inspection. No adverse reactions have been reported.

    Product
    Coco's Italian Market Recalls Italian Meatball, Beef Ravioli, and Pepperoni Pizza Products Produced without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereCPSC·20765·2020-07-23

    Polaris Recalls Ranger, PRO XD, and Bobcat Utility Vehicles Due to Crash Hazard

    Polaris is recalling approximately 13,200 Ranger, PRO XD, and Bobcat utility vehicles because a defective clutch component can cause unexpected motion, posing a crash hazard.

    Product
    Model Year 2020 Ranger XP 1000 and Ranger CREW XP 1000 Off-Road Vehicles, Model Years 2019 - 2020 PRO XD 4000D UTVs, Model Year 2019 PRO XD 2000D UTVs, and Model Year 2020 Bobcat UV34 and UV34XL UTVs
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2553-2020·2020-07-22

    CME BodyGuard BodySet Infusion Sets Recalled for Delivery Inaccuracy

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

    Product
    BodyGuard BodySet, REF: A120-160SAS
    Category
    Medical Device
    Distribution
    49 states
  • CriticalFDA (Devices)·Z-2567-2020·2020-07-22

    CME America Recalls BodyGuard Microset Infusion Sets Due to Delivery Inaccuracy

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

    Product
    BodyGuard Microset with Needleless Adaptor, REF: A120-003XSNY
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Food)·F-1109-2020·2020-07-22

    Fresh Express Recalls Hy-Vee Shredded Lettuce Due to Cyclospora Risk

    Fresh Express is recalling Hy-Vee Shredded Lettuce due to a possible health risk from Cyclospora. The product was distributed in 33 U.S. states and Canada.

    Product
    Hy-Vee Shredded Lettuce 8 oz., UPC 075450120530, Iceberg lettuce
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-2569-2020·2020-07-22

    CME America Recalls CMExpress Microbore Sets Due to Delivery Inaccuracy

    CME America is recalling CMExpress Microbore Sets because they may deliver therapy at inaccurate rates, potentially causing over-infusion or under-infusion.

    Product
    CMExpress Microbore Set, REF: A120-161CYF
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Devices)·Z-2596-2020·2020-07-22

    Skeletal Kinetics Recalls Acumed Impact Bone Void Filler Kits

    Skeletal Kinetics is recalling 41 units of Acumed Impact 5CC bone void filler kits because they may not maintain setting characteristics for the labeled shelf-life.

    Product
    ACUMED IMPACT 5CC. Product Number: 65-0105-S, UDI: 813845020252 - Product Usage: Callos is indicated to fill bony voids or gaps of the skeletal system (i.e. extremities, spine, pelvis). These defects may be surgically created osseous defects or osseous defects created from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2585-2020·2020-07-22

    CME America Recalls Infusion Sets Due to Delivery Inaccuracy

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

    Product
    Standard BodySet with Needleless Connectors, REF: A120-125XS
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Food)·F-1082-2020·2020-07-22

    Fresh Express Veggie Spring Mix Recalled for Cyclospora Risk

    Fresh Express is recalling Veggie Spring Mix 7 oz. bags due to a possible health risk from Cyclospora contamination.

    Product
    Fresh Express Veggie Spring Mix 7 oz., UPC 071279281049, Baby lettuce, carrots, red cabbage & radishes
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Devices)·Z-2580-2020·2020-07-22

    CME America Recalls CMExpress Microbore Sets Due to Delivery Inaccuracy

    CME America is recalling CMExpress Microbore Sets because they may deliver therapy at inaccurate rates, potentially causing over-infusion or under-infusion.

    Product
    CMExpress Microbore Sets, REF: A120-161C
    Category
    Medical Device
    Distribution
    49 states
  • SevereFDA (Food)·F-1056-2020·2020-07-22

    Fresh Express Chopped Kit Bacon & Bleu Recalled for Cyclospora Risk

    Fresh Express is recalling Chopped Kit Bacon & Bleu salads due to a possible health risk from Cyclospora. Consumers should not eat the product.

    Product
    Fresh Express Chopped Kit Bacon & Bleu 10.9 oz, UPC 071279306063, Red and green cabbage, green leaf lettuce, carrots & green onions
    Category
    Food
    Distribution
    32 states
  • SevereFDA (Food)·F-1072-2020·2020-07-22

    Fresh Express Iceberg Garden Salad Recalled for Cyclospora Risk

    Fresh Express is recalling Iceberg Garden salad products due to a possible health risk from Cyclospora. Consumers should check their refrigerators for affected lots.

    Product
    Fresh Express Iceberg Garden / Lechuga Repollo 3 lbs., UPC 071279104119, Iceberg lettuce, carrots & red cabbage
    Category
    Food
    Distribution
    32 states