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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15876–15900 of 39592

  • SevereFDA (Devices)·Z-0893-2019·2019-03-06

    Philips Achieva 3.0T MRI System Recalled Due to Ceiling Speaker Hazard

    Philips is recalling 11,226 Achieva 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Achieva 3.0T, Model Number 781177. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0926-2019·2019-03-06

    Philips MR RT MRI Systems Recalled for Falling Ceiling Speaker Hazard

    Philips is recalling MR RT MRI systems because ceiling speakers may fall due to magnetic attraction.

    Product
    MR RT, Model Number 781439. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V188000·2019-03-06

    Volkswagen Recalls 56,173 Vehicles for Rear Coil Spring Fracture Risk

    Volkswagen is recalling 56,173 vehicles because rear coil springs may fracture prematurely, potentially causing tire damage and loss of vehicle control.

    Product
    VOLKSWAGEN — VOLKSWAGEN TIGUAN, GOLF SPORTWAGEN, GOLF, JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1067-2019·2019-03-06

    Ottogi Ppushu Ppushu Grilled Chicken Flavor Noodles Recalled for Undeclared Egg

    Ottogi America Inc. is recalling 1,594,338 units of Ppushu Ppushu Grilled Chicken Flavor noodles due to an undeclared egg allergen.

    Product
    Ottogi Ppushu Ppushu Grilled Chicken Flavor 3.17oz x 40ea Item #21503006 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • SevereNHTSA·19V178000·2019-03-06

    Entegra Recalls 2019-2020 Reatta Motorhomes for Damaged Tow Hitch

    Entegra Coach is recalling 2019-2020 Reatta motorhomes because the tow hitch may have been damaged during delivery, increasing the risk of a crash.

    Product
    ENTEGRA — ENTEGRA REATTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0895-2019·2019-03-06

    Philips Intera 1.5T MRI System Recalled for Ceiling Speaker Hazard

    Philips is recalling Intera 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera 1.5T, Model Number 781195. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1090-2019·2019-03-06

    Produce Packaging Inc Recalls Combo Stir Fry Fajita Packs Due to E. coli Risk

    Produce Packaging Inc is recalling Combo, Stir Fry/Fajita 6 PK products due to potential E. coli contamination. The products were distributed in Ohio, Michigan, New York, and Texas.

    Product
    Produce Packaging, Inc. Combo, Stir Fry/Fajita 6 PK
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1071-2019·2019-03-06

    Ottogi Beijing Spicy Seafood Noodles Recalled for Undeclared Egg Allergen

    Ottogi America is recalling Beijing Spicy Seafood Noodles because they contain egg, which is not listed on the label.

    Product
    Ottogi Beijing Spicy Seafood Noodle 5PK 1lb 5.16oz x 8pk Item #32142408 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Food)·F-1062-2019·2019-03-06

    Ottogi Jin Ramen Spicy Bowl Recalled for Undeclared Egg Allergen

    Ottogi America Inc. is recalling specific lots of Ottogi Jin Ramen Spicy Bowl due to an undeclared egg allergen. Consumers should check their pantry and stop eating the product.

    Product
    Ottogi Jin Ramen Spicy, Bowl, 5PK 4.23oz x 20ea, 3.88oz x 12ea, 1lb 5.16oz x 8pk Item #21501202, 21502155, 32142402 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Food)·F-1072-2019·2019-03-06

    Ottogi Spicy Seafood Udon Noodles Recalled for Undeclared Egg Allergen

    Ottogi America is recalling Spicy Seafood Udon noodles due to an undeclared egg allergen. Consumers with egg allergies should not consume the product.

    Product
    Ottogi Spicy Seafood flavor Udon Odongtong 5PK 1lb 5.16oz x 8pk Item #32142410 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Food)·F-1091-2019·2019-03-06

    Produce Packaging Inc. Recalls Stir-Fry Mix Due to E. coli Risk

    Produce Packaging Inc. is recalling 525 units of 9 LB Stir-Fry Mix due to potential E. coli contamination. The product was distributed in Ohio, Michigan, New York, and Texas.

    Product
    Produce Packaging, Inc. Mix, Stir-Fry WG 9 LB
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1083-2019·2019-03-06

    Produce Packaging Inc Recalls Vegetable Trays Due to E. coli Risk

    Produce Packaging Inc is recalling 12-inch vegetable trays due to a potential E. coli contamination risk identified by a supplier.

    Product
    Produce Packaging, Inc. Tray, Veg - Fishers 12"
    Category
    Consumer Product
    Distribution
    4 states
  • SevereFDA (Food)·F-1123-2019·2019-03-06

    Whole Foods Market Recalls Mesclun Mix Due to Salmonella Contamination

    Whole Foods Market is recalling Mesclun Mix With Candied Pecans and Sun Dried Cranberries due to potential Salmonella contamination. The product was distributed in eight northeastern and southeastern states.

    Product
    Mesclun Mix With Candied Pecans and Sun Dried Cranberries packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0863-2019·2019-03-06

    Physio-Control Recalls LIFEPAK 15 Monitor/Defibrillator Service Kits

    Physio-Control is recalling 682 LIFEPAK 15 Monitor/Defibrillator service kits because they may lock up after delivering a shock, leaving the monitor display blank.

    Product
    LIFEPAK 15 Monitor/Defibrillator service kits Product Usage: The LIFEPAK(R) 15 Monitor/defibrillator (LP15) is a complete acute cardiac care response system designed for basic life support (BLS) and advanced life support (ALS) patient management protocols. The LP15…
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-1073-2019·2019-03-06

    Ottogi Buckwheat Chilli Noodles Recalled for Undeclared Egg Allergen

    Ottogi America is recalling Buckwheat Chilli Noodles because they contain egg, which is not listed on the label.

    Product
    Ottogi BuckwheatChilli Noodle PK 1lb 6.93oz x 8pk Item #32143061 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Devices)·Z-0873-2019·2019-03-06

    Philips Multiva MRI System Recalled Due to Ceiling Speaker Hazard

    Philips is recalling 11,226 Multiva MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Multiva 1.5T 16 R5, Model Number 781078. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0862-2019·2019-03-06

    Physio-Control Recalls LIFEPAK 15 Monitor/Defibrillators Due to Lockup Condition

    Physio-Control is recalling 13,005 LIFEPAK 15 Monitor/Defibrillators because they may lock up after delivering a shock, leaving the display blank and unresponsive.

    Product
    LIFEPAK 15 Monitor/Defibrillator Product Usage: The LIFEPAK(R) 15 Monitor/defibrillator (LP15) is a complete acute cardiac care response system designed for basic life support (BLS) and advanced life support (ALS) patient management protocols. The LP15 monitor/defibrillator…
    Category
    Medical Device
    Distribution
    0 states
  • SevereFDA (Food)·F-1063-2019·2019-03-06

    Ottogi Snack Ramen Recalled for Undeclared Egg Allergen

    Ottogi America is recalling specific lots of Ottogi Snack Ramen cups because they contain egg, which is not listed on the label.

    Product
    Ottogi Snack Ramen 5PK, Cup 1lb 3.05oz x 8pk, 2.18oz x 6ea Item #21501281, 21502161 Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249
    Category
    Food
    Distribution
    12 states
  • SevereFDA (Food)·F-1077-2019·2019-03-06

    Produce Packaging Inc. Recalls Rice Cauliflower Due to E. coli Risk

    Produce Packaging Inc. is recalling 5 LB packages of Rice Cauliflower due to potential E. coli contamination. The product was distributed in Ohio, Michigan, New York, and Texas.

    Product
    Produce Packaging, Inc. Cauliflower, Rice 5 LB
    Category
    Food
    Distribution
    4 states
  • SevereFDA (Food)·F-1104-2019·2019-03-06

    Whole Foods Quinoa with Dark Leafy Greens Recalled for Salmonella Risk

    Whole Foods Market is recalling Quinoa with Dark Leafy Greens due to potential Salmonella contamination. The product was sold in eight northeastern and southeastern states.

    Product
    Quinoa with Dark Leafy Greens packaged in plastic nonflexible containers
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Devices)·Z-0876-2019·2019-03-06

    Philips Intera 1.0T MRI System Recalled for Ceiling Speaker Hazard

    Philips is recalling Intera 1.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.

    Product
    Intera 1.0T Power/Pulsar, Model Number 781103. Nuclear Magnetic Resonance Imaging System
    Category
    Medical Device
    Distribution
    Distributed nationwide