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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11226–11250 of 36635

  • SevereNHTSA·20V323000·2020-06-04

    Braun Recalls 2019-2020 Demers Ambulances for Rear Brake Line Wear

    Braun Ambulances is recalling 31 Demers ambulances because a rear brake line may wear, causing brake failure and increasing crash risk.

    Product
    DEMERS AMBULANCES — DEMERS AMBULANCES TYPE I (MXP150E), TYPE I (MXP170E)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V324000·2020-06-04

    GM Recalls 2020 Chevrolet and GMC Trucks for Hood Latch Defect

    General Motors is recalling 2020 Chevrolet Silverado and GMC Sierra trucks because improperly heat-treated hood-latch striker wires may fracture, allowing the hood to open while driving.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 3500, SILVERADO 2500, SIERRA 3500, SIERRA 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2107-2020·2020-06-03

    MPS Top Cover Replacement Kit Recalled Due to Swapped Labels

    Quest Medical is recalling MPS Top Cover Replacement Kits because additive and arrest agent labels were swapped, posing a risk of over-delivering potassium during surgery.

    Product
    Ref 801168, MPS Top Cover Replacement Kit, 1 UNITS, UDI: (01)2 0634624 81168 7 (11)190916 (17)290913 (10)059135 (The device is a component of the MPS Console used as replacements for worn or damaged MPS Console top covers)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2146-2020·2020-06-03

    Biomet Recalls Regenerex Knee Prostheses Due to Potential Endotoxin Levels

    Biomet is recalling 15 units of Regenerex Series-A Patella knee prostheses due to potential endotoxin levels exceeding specifications.

    Product
    Knee Products: 141356 Regenerex Series-A Patella 3 Peg, 31 MM 141358 Regenerex Series-A Patella 3 Peg, 37 MM Product Usage: Knee prosthesis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2118-2020·2020-06-03

    Clinical Innovations Recalls Clearview Total Uterine Manipulator Due to Defective Tip Support

    Clinical Innovations is recalling 280 Clearview Total Uterine Manipulators (model UM750) because a missing notch on the tip support may prevent proper attachment of surgical components.

    Product
    Clearview Total Uterine Manipulator (model UM750), The device is labeled in part, "ClearView(R) TOTAL, 7 cm* * *CLINICAL INNOVATIONS Manufacturer: Clinical Innovations, LLC* * *Reorder Number: UM750* * *LOT 181183* * *." Each device is accompanied by Instruction for Use which…
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Devices)·Z-2128-2020·2020-06-03

    Siemens Cios Spin X-Ray System Recalled for Electrical Shock Risk

    Siemens is recalling 20 Cios Spin X-Ray systems because unplugging the monitor cable can create unsafe voltage, posing an electrical shock hazard.

    Product
    Cios Spin Image-Intensified Fluoroscopic X-Ray System, Model Numbers VA30-10308194
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2056-2020·2020-06-03

    Heartware Recalls HVAD Pump Implant Kits Due to Graft Tears and Screw Breakage

    Heartware, Inc. is recalling 2,225 HVAD Pump Implant Kits because the outflow graft may tear and the strain relief screw may break during pre-implant assembly.

    Product
    Heartware HVAD Pump Implant Kit, Product (REF) Number 1104
    Category
    Medical Device
    Distribution
    0 states
  • SevereNHTSA·20V320000·2020-06-01

    Keystone Recalls 2020 Springdale Trailers Due to Incorrect Axles and Tires

    Keystone RV Company is recalling 2020 Springdale trailers because they were equipped with incorrect axles and tires, which may cause the trailer to be overloaded and increase the risk of a crash.

    Product
    KEYSTONE — KEYSTONE SPRINGDALE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V317000·2020-05-29

    Forest River Recalls 2020-2021 Cargo Trailers Due to Safety Chain Defect

    Forest River is recalling 2020-2021 US Cargo, Haulin', and Trail & Sport cargo trailers because safety chains may break if the trailer becomes unhitched.

    Product
    US CARGO — US CARGO, HAULIN' CARGO TRAILER, TRAIL & SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V316000·2020-05-29

    Braun Ambulances Recall 2019 Models Due to Rear Brake Line Wear

    Braun Ambulances is recalling 2019 Chief XL and Liberty ambulances because a rear brake line may wear, causing brake failure and increasing crash risk.

    Product
    BRAUN AMBULANCES — BRAUN AMBULANCES CHIEF XL TYPE I, LIBERTY TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V313000·2020-05-28

    Frazer Recalls 2019-2020 RAM Chassis Emergency Vehicles for Brake Line Wear

    Frazer is recalling 2019-2020 emergency vehicles on RAM 4500 and 5500 chassis because rear brake lines may wear, causing brake failure and increasing crash risk.

    Product
    FRAZER — FRAZER RAM 4500 CHASSIS, RAM 5500 CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V314000·2020-05-28

    Honda and Acura Recall Vehicles for Fuel Pump Failure Risk

    Honda is recalling specific 2018-2020 models because a faulty fuel pump may cause the engine to stall while driving, increasing crash risk.

    Product
    HONDA — HONDA, ACURA ACCORD, INSIGHT, CIVIC, RLX HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·011-2020·2020-05-28

    Nestle Recalls Lean Cuisine Fettuccini Alfredo for Undeclared Allergens

    Nestle Prepared Foods is recalling Lean Cuisine Fettuccini Alfredo products because they contain undeclared soy and chicken, which are not listed on the label.

    Product
    Nestle Prepared Foods Company — Nestle Prepared Foods Company Recalls Lean Cuisine Fettuccini Alfredo Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V312000·2020-05-28

    Thor Motor Coach Recalls 2020 Motorhomes for Brake Hose Chafing Risk

    Thor Motor Coach is recalling 566 2020 motorhomes because a fender liner may chafe the brake hose, potentially causing brake fluid loss and increased braking distance.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH SIESTA, CHATEAU CITATION, TIBURON, COMPASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0964-2020·2020-05-27

    Peekaboo Organic Mint Chocolate Chip Ice Cream Recalled for Listeria

    Ramar International is recalling Peekaboo Organic Mint Chocolate Chip ice cream because it tested positive for Listeria monocytogenes.

    Product
    Peekaboo Ice Cream + hidden Veggies; Organic Mint Chocolate Chip with Hidden Spinach, 14 oz. carton: UPC: 868540000115 Manufactured for: Peekaboo Organics LLC, Surfside, FL. 33154 Certified Organic by QCS
    Category
    Food
    Distribution
    1 state
  • CriticalFDA (Food)·F-0947-2020·2020-05-27

    Condies Foods Recalls Chicken Salad Croissants Due to Undeclared Soy Allergen

    Condies Foods, Inc. is recalling 104 chicken salad croissants in Utah because they contain undeclared soy. The error occurred when the wrong ingredient was purchased and used.

    Product
    43237 ROLL chicken salad on croissant single, vacuumed pack bag, Clam shell. Label UPC: 50777445351, Condies Foods Inc. PO Box 18548. Salt Lake City, UT.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Devices)·Z-2022-2020·2020-05-27

    K2M Aleutian Lordotic Spreader Recalled Due to Tip Breakage Risk

    K2M, Inc. is recalling Aleutian Lordotic Spreaders because the welded tips may break off during spinal procedures.

    Product
    K2M, ALEUTIAN Interbody Spacer Systems, EN AN Lordotic Spreader, Stainless Steel, Non-Sterile, Qty 1, Catalog # 5203-90153, UDI # 10888857108660, Size 28x8mm, 6 Product Usage: Used to simulate the height of the cage and expand the spine disc space to determine the optimal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2017-2020·2020-05-27

    K2M Aleutian Lordotic Spreader Recalled Due to Tip Breakage Risk

    K2M, Inc. is recalling the Aleutian Lordotic Spreader because the welded tip may break off during spinal procedures.

    Product
    K2M, ALEUTIAN Interbody Spacer Systems, EN AN Lordotic Spreader, Stainless Steel, Non-Sterile, Qty 1, Catalog # 5203-90135, UDI # 10888857108486, Size 24x4mm, 18 Product Usage: Used to simulate the height of the cage and expand the spine disc space to determine the optimal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2060-2020·2020-05-27

    Bovie Medical Recalls Renuvion J-Plasma Precise Open Handpieces Due to Fracture Risk

    Bovie Medical Corporation is recalling Renuvion/J-Plasma Precise Open Handpieces because unexpected stress fractures may cause the shaft to fragment during clinical use.

    Product
    Renuvion/ J-Plasma Precise Open Handpiece. Catalog numbers BVX-044-BPS, BVX-044-BPP, BVX-150-BPP, BVX-150-BPS, APYX-044-BPS, APYX-150-BPP, and APYX-150-BPS - Product Usage: for electrosurgical cutting, coagulation and ablation of soft tissue during open surgical procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2015-2020·2020-05-27

    K2M Aleutian Lordotic Spreader Recalled Due to Tip Breakage Risk

    K2M, Inc. is recalling the Aleutian Lordotic Spreader because the welded tip may break off during spinal procedures.

    Product
    K2M, ALEUTIAN Interbody Spacer Systems, EN AN Lordotic Spreader, Stainless Steel, Non-Sterile, Qty 1, Catalog # 5203-90125, UDI # 10888857108387, Size 24x8mm, 12 Product Usage: Used to simulate the height of the cage and expand the spine disc space to determine the optimal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2009-2020·2020-05-27

    K2M Recalls Aleutian Lordotic Spreader Due to Tip Breakage Risk

    K2M, Inc. is recalling the Aleutian Anatomically Narrow Lordotic Spreader because the welded tip may break off during spinal procedures.

    Product
    K2M, ALEUTIAN Interbody Spacer Systems, EN AN Lordotic Spreader, Stainless Steel, Non-Sterile, Qty 1, Catalog # 5203-90109, UDI # 10888857108226, Size 24x6mm, 6 Product Usage: Used to simulate the height of the cage and expand the spine disc space to determine the optimal…
    Category
    Medical Device
    Distribution
    Distributed nationwide