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.

Filters

Agency

Category

Minimum severity

Clear filters

14051–14075 of 36679

  • SevereFDA (Devices)·Z-1666-2019·2019-06-05

    Maquet Getinge NICU ECC Pack Recall Due to Sterility Assurance Concerns

    Maquet Cardiovascular is recalling NICU ECC Packs because a design feature may prevent sterilization gas from reaching all fluid paths, compromising sterility.

    Product
    Maquet Getinge- BEQ-TOP 39202 NICU ECC PACK Material: 701067313R01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1429-2019·2019-06-05

    Suja Organic Kombucha Recalled Due to Glass Fragments

    Suja Life LLC is recalling 64,896 bottles of Organic Kombucha - Ginger Lemon due to consumer complaints of finding pieces of glass in the product.

    Product
    Suja Organic Kombucha - Ginger Lemon: 15.2 oz. glass bottle; UPC 818617020232 DISTRIBUTED BY SUJA LIFE, LLC OCEANSIDE, CA 92056 CERTIFIED ORGANIC BY CCOF SUJAJUICE.COM
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Devices)·Z-1669-2019·2019-06-05

    Maquet Cardiovascular Recalls Custom Tubing Sets for Sterility Assurance Concerns

    Maquet Cardiovascular is recalling specific custom tubing sets for extracorporeal circulation because a design flaw may prevent proper sterilization, potentially compromising sterility.

    Product
    Maquet Getinge- (1) Material :701067370R01 BO-TOP 38803 OPEN HEART PACK W (2) Material: 701067370R02 BO-TOP 38803 OPEN HEART PACK W (3) Material: 701067370R03 BO-TOP 38803 OPEN HEART PACK W
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1507-2019·2019-06-05

    Maquet Getinge-BEQ-TOP 5900 Custom Tubing Sets Recalled for Sterility Concerns

    Maquet Cardiovascular is recalling specific custom tubing sets for extracorporeal circulation because a design flaw may prevent proper sterilization, potentially compromising sterility.

    Product
    Maquet Getinge-BEQ-TOP 5900 3/8 Quadrox iD Pack w/BB Material: 701050228
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1427-2019·2019-06-05

    Global Pride Rattan Shoots Recalled for Undeclared Sulfites

    U.S. Tov, Inc. is recalling Global Pride Rattan Shoots in Brine because testing found high levels of undeclared sulfites.

    Product
    Global Pride Rattan Shoots in Brine: 24 oz. glass jar UPC: 8855273023148 Erawan Enterprise Co. Ltd Bangkok, Thailand. Ingredients: Rattan 50.6%, Water 48.9%, Citric Acid (E330) 0.5%
    Category
    Food
    Distribution
    23 states
  • SevereFDA (Food)·F-1426-2019·2019-06-05

    Biltmore Smoked Salmon Recalled Due to Listeria Monocytogenes Contamination

    Seven Seas International USA LLC is recalling Biltmore Sashimi Grade Smoked Wild Sockeye Salmon because the product tested positive for Listeria monocytogenes.

    Product
    Biltmore, Sashimi Grade Smoked Wild Sockeye All Natural Alaskan Salmon, 4 oz. (113g)
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Devices)·Z-1521-2019·2019-06-05

    Maquet Getinge-BEQ-TOP 25500 ECC Tubing Sets Recalled for Sterility Assurance Issues

    Maquet Cardiovascular is recalling specific Custom Tubing Sets for Extracorporeal Circulation because the design may prevent proper sterilization gas flow, compromising sterility.

    Product
    Maquet Getinge-BEQ-TOP 25500 ECC 3/8 w/QiD Material: 701052461
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1574-2019·2019-06-05

    Maquet Getinge ECC Pump Packs Recalled for Sterility Assurance Concerns

    Maquet Cardiovascular is recalling specific ECC Pump Packs because a design feature may prevent proper sterilization, potentially compromising sterility.

    Product
    Maquet Getinge-BEQ-TOP 30907 ECC PUMP PACK Material: 701065770
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1660-2019·2019-06-05

    Maquet Getinge Custom Tubing Sets Recalled for Sterility Assurance Concerns

    Maquet Cardiovascular is recalling specific custom tubing sets for extracorporeal circulation because a design feature may prevent proper sterilization, potentially compromising sterility.

    Product
    Maquet Getinge- BEQ-T 5211 ECC Large Children's Hospital Material: 701064560R01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1615-2019·2019-06-05

    Maquet Cardiovascular Recalls Custom Tubing Sets for Extracorporeal Circulation

    Maquet Cardiovascular is recalling custom tubing sets for extracorporeal circulation because a design flaw may prevent sterilization gas from reaching all parts of the device.

    Product
    Maquet Getinge-BEQ-T 36507 Accessory Pk Mercy Material: 709000390
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1536-2019·2019-06-05

    Maquet Getinge-T Sample Manifold Recalled Due to Sterility Assurance Concerns

    Maquet Cardiovascular is recalling specific Sample Manifolds because a design feature may prevent sterilization gas from reaching all fluid paths, potentially compromising sterility.

    Product
    Maquet Getinge-T 22706 SAMPLE MANIFOLD Material:701054912
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1652-2019·2019-06-05

    Maquet Getinge E-Circuit Bioline Heparin Tubing Sets Recalled for Sterility Concerns

    Maquet Cardiovascular is recalling specific batches of BEQ-TOP 37200 E-Circuit Bioline Heparin tubing sets because a design feature may prevent proper sterilization, potentially compromising sterility.

    Product
    Maquet Getinge- BEQ-TOP 37200 E-Circuit Bioline Heparin Material: 701055388R01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V411000·2019-06-04

    Ferrari Recalls Multiple Models Due to Air Bag Control Module Malfunction

    Ferrari is recalling 893 vehicles because the air bag control module may malfunction, potentially causing air bags or seat belt pretensioners to fail to deploy or deploy improperly.

    Product
    FERRARI — FERRARI F12 BERLINETTA, CALIFORNIA T, 488 GTB, 488 SPIDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19750·2019-06-04

    Polaris Recalls 2015-2019 Ranger EV Vehicles Due to Crash Hazard

    Polaris is recalling about 3,900 Ranger EV recreational off-highway vehicles due to a wiring defect that can cause unexpected acceleration and crashes.

    Product
    Model Year 2015 - 2019 Polaris RGR EV recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V412000·2019-06-04

    Honda Recalls 2018-2019 Motorcycles Due to Transmission Shaft Defect

    Honda is recalling specific 2018 and 2019 motorcycles because a transmission part may detach, causing gear misalignment that increases crash risk.

    Product
    HONDA — HONDA CB300R, CMX300, CRF250L, CBR300R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·064-2019·2019-05-31

    Perdue Recalls Chicken Products Due to Possible Bone Contamination

    Perdue Foods is recalling approximately 31,703 pounds of ready-to-eat chicken products that may contain pieces of bone material.

    Product
    PERDUE FOODS, LLC. — Perdue Foods LLC Recalls Perdue Simply Smart Organics Poultry Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·063-2019·2019-05-31

    Johnsonville Recalls Jalapeno Cheddar Sausage Due to Plastic Contamination

    Johnsonville is recalling ready-to-eat jalapeno cheddar smoked sausage links due to possible hard green plastic contamination. No adverse reactions have been reported.

    Product
    Johnsonville, LLC — Johnsonville, LLC. Recalls Ready-To-Eat Jalapeno Cheddar Smoked Sausage Links Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·062-2019·2019-05-31

    Los Hernandez Tamales Recalls Chicken and Pork Products Produced Without Inspection

    Los Hernandez Tamales LLC is recalling approximately 9,090 pounds of chicken and pork tamales produced without federal inspection. No adverse reactions have been reported.

    Product
    Los Hernandez Tamales LLC — Los Hernandez Tamales, LLC Recalls Chicken and Pork Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·19V406000·2019-05-30

    Jayco Recalls 2020 Greyhawk Motorhomes Due to Brake Valve Defect

    Jayco is recalling 2020 Greyhawk motorhomes because a defective brake relay valve may cause extended stopping distances, increasing crash risk.

    Product
    JAYCO — JAYCO GREYHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V403000·2019-05-30

    Mazda Recalls 2018 CX-9 Vehicles Due to Wiring Harness Defect

    Mazda is recalling 2018 CX-9 vehicles because a wiring harness defect may disable the passenger air bag, turn signals, or engine starting system.

    Product
    MAZDA — MAZDA CX-9
    Category
    Vehicle
    Distribution
    Distributed nationwide