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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16176–16200 of 39592

  • SevereFDA (Food)·F-0856-2019·2019-02-13

    Spokane Produce Recalls Turkey Hoagies for E. Coli O157:H7 Risk

    Spokane Produce Inc is recalling Turkey Hoagie w/Avocado Spread sandwiches due to potential E. Coli O157:H7 contamination. The recall covers 200 units distributed in five western states.

    Product
    Turkey Hoagie w/Avocado Spread sandwich is a Hoagie bread made with Turkey, Processed Swiss Cheese, green leaf and avocado spread. -Turkey Hoagie w/Avocado Spread, 7 oz, UPC 88694 79816, Northwest Cuisine Creations brand. -Turkey Hoagie w/Avocado Spread, 7 oz, UPC 88694…
    Category
    Food
    Distribution
    5 states
  • SevereFDA (Devices)·Z-0713-2019·2019-02-13

    Smiths Medical Recalls Portex Sterile Water Pour Bottles Due to Leaking

    Smiths Medical is recalling Portex 500 ml Sterile Water USP Pour Bottles because leaking containers may compromise sterility and expose users to infectious agents.

    Product
    Portex 500 ml Sterile Water USP Pour Bottle¿¿¿¿ ¿¿¿
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0790-2019·2019-02-13

    Pizza Blends Recalls Custom Pizza Flour Due to Salmonella Risk

    Pizza Blends, LLC is recalling 198 cases of Village Pizza & Seafood Custom Pizza Flour because an ingredient may be contaminated with Salmonella.

    Product
    Village Pizza & Seafood, Custom Pizza Flour, Manufactured Exclusively for Village Pizza & Seafood League City, TX, packaged in 21.7 lb bags.
    Category
    Food
    Distribution
    18 states
  • SevereNHTSA·19V096000·2019-02-13

    BMW Recalls 2019 X5 Models for Loose Driver's Seat Bolts

    BMW is recalling 2019 X5 xDrive40i and xDrive50i vehicles because driver's seat and seat belt bolts may not be properly tightened, increasing injury risk in a crash.

    Product
    BMW — BMW X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V093000·2019-02-12

    Freightliner Cascadia Recall for Tie-Rod Failure Risk

    Daimler Trucks North America is recalling 2013-2016 Freightliner Cascadia trucks because brake vibrations may cause tie-rod failure, leading to loss of steering.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·015-2019·2019-02-11

    Panola County Processing Recalls Sausage Products Due to Processing Deviation

    Panola County Processing LLC is voluntarily recalling approximately 59 pounds of smoked sausage products due to a processing deviation that may have led to underprocessing.

    Product
    Panola County Processing LLC — Panola County Processing, LLC Recalls Sausage Products Due to Possible Processing Deviation
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·19V078000·2019-02-11

    Forest River Recalls 2019 Columbus Trailers Due to Hitch Bolt Issue

    Forest River is recalling 2019 Columbus recreational trailers because insufficiently tightened pin box mounting bolts could cause the trailer to separate from the tow vehicle.

    Product
    FOREST RIVER — FOREST RIVER COLUMBUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·014-2019·2019-02-10

    VICS Acquisition Recalls Chicken Products Due to Undeclared Egg Allergen

    VICS Acquisition, LLC is recalling approximately 99,975 pounds of frozen chicken products because they contain eggs, a known allergen, that is not declared on the label.

    Product
    VICS Acquisition, LLC — VICS Acquisition, LLC Recalls Chicken Products due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    7 states
  • SevereNHTSA·19V088000·2019-02-07

    GM Recalls 2016-2018 Silverado and Sierra 3500 Trucks for Fuel Tank Fire Risk

    General Motors is recalling 2016-2018 Chevrolet Silverado 3500 and GMC Sierra 3500 trucks because a fuel sensor defect may cause the front tank to overfill, potentially leading to a fuel leak and fire.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 3500, SIERRA 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V066000·2019-02-07

    Freightliner Recalls Cascadia Trucks Due to Air Bag Deployment Risk

    Daimler Trucks is recalling 2018-2020 Freightliner Cascadia trucks because the driver's frontal air bag may deploy unexpectedly, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1053-2019·2019-02-06

    ALDI Rio Duero Plums Recalled for Listeria Contamination Risk

    Jac Vandenberg Inc. is recalling Rio Duero plums sold at ALDI due to potential Listeria monocytogenes contamination.

    Product
    Plums sold at ALDI, packaged in a 2-pound bag with the brand Rio Duero, EAN# 7804650090304.
    Category
    Food
    Distribution
    18 states
  • CriticalFDA (Devices)·Z-0765-2019·2019-02-06

    Edwards Lifesciences Recalls Swan Ganz Catheters Due to Lumen Reversal

    Edwards Lifesciences is recalling 459 Swan Ganz Thermodilution Catheters because incorrect lumen assembly causes reversed pressure readings, potentially leading to misdiagnosis.

    Product
    Edwards Lifesciences Swan Ganz Thermodilution Catheter, REF 151F7 Product Usage: The Swan-Ganz Thermodilution Catheter provides a diagnostic tool for physicians to rapidly determine hemodynamic pressures and cardiac output when used with a compatible cardiac output computer.…
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Devices)·Z-0764-2019·2019-02-06

    Edwards Lifesciences Recalls Swan Ganz Catheters Due to Lumen Assembly Error

    Edwards Lifesciences is recalling 9 units of Swan Ganz Thermodilution Catheters because incorrect lumen assembly causes reversed pressure readings.

    Product
    Edwards Lifesciences Swan Ganz Thermodilution Catheter, REF 131VF7P Product Usage: The Swan-Ganz Thermodilution Catheter provides a diagnostic tool for physicians to rapidly determine hemodynamic pressures and cardiac output when used with a compatible cardiac output…
    Category
    Medical Device
    Distribution
    0 states
  • CriticalFDA (Food)·F-1051-2019·2019-02-06

    Jac Vandenberg Recalls Chilean Peaches Due to Listeria Contamination Risk

    Jac Vandenberg Inc. is recalling bulk peaches from Chile and Rio Duero brand peaches sold at Aldi due to potential Listeria monocytogenes contamination.

    Product
    Peaches, sold as a bulk retail item, with PLU 4044, and country of origin of Chile. The peaches sold at Aldi are packaged in a two pound bag with the brand Rio Duero, EAN# 7804650090281.
    Category
    Food
    Distribution
    18 states
  • CriticalFDA (Food)·F-0936-2019·2019-02-06

    Dakota Specialty Milling Enhanced Flax Flour Blend Recalled for Salmonella Risk

    Dakota Specialty Milling is recalling Enhanced Flax Flour Blend because an ingredient may be contaminated with Salmonella. The product was distributed in California, Ohio, and Texas.

    Product
    Dakota Specialty Milling Enhanced Flax Flour Blend, 42205, Net Wt 50 lbs. Ground Flax, Calcium Sulfate, inulin, VM 112 (vitamin mix flour enrichment containing Niacin, Iron, Vitamin B-1, Vitamin B-2, Folic Acid, Wheat Starch)
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0761-2019·2019-02-06

    Glass Onion Catering Recalls Hummus and Quinoa Wraps Due to Undeclared Soy

    Atherstone Foods, Inc. dba Glass Onion Catering is recalling 114 units of Hummus & Quinoa Tabouleh Wraps because mayonnaise containing soy was used in error, and the product label does not declare soy as an allergen.

    Product
    greens & Grains Hummus & Quinoa Tabouleh Wrap with lemon tahini dressing: Perishable: Keep Refrigerated Plastic container with tamper proof hinged lid Use by 12/19/18 Incorrect dressing was used: Label states: Dressing: Tahini (ground sesame seeds), Lemon Juice, Water…
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0412-2019·2019-02-06

    Prinston Recalls Irbesartan and Hydrochlorothiazide Tablets Due to NDEA Impurity

    Prinston Pharmaceutical Inc. is recalling Irbesartan and Hydrochlorothiazide tablets because FDA testing found the impurity NDEA above acceptable limits.

    Product
    IRBESARTAN AND HYDROCHLOROTHIAZIDE — IRBESARTAN AND HYDROCHLOROTHIAZIDE (IRBESARTAN AND HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0769-2019·2019-02-06

    West Pharma Services Recalls Vial2BAG DC 20mm Medical Devices

    West Pharma Services is recalling Vial2BAG DC 20mm devices because adverse events were reported with the similar 13mm model used with oxytocin in pregnant women.

    Product
    Vial2BAG DC 20mm: 1) REF 6070112 & 2) REF 6070112C, Single use only, Rx Only
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Devices)·Z-0768-2019·2019-02-06

    FDA Recalls Vial2BAG Transfer Device Due to Reported Adverse Events

    West Pharma Services is recalling Vial2BAG Transfer Devices because adverse events were reported when used with oxytocin in pregnant women.

    Product
    Vial2BAG Transfer Device, REF 6070104, Single use only, Rx Only
    Category
    Medical Device
    Distribution
    1 state