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 deaths or serious injuries are reported, 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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601–625 of 7436

  • CriticalFDA (Food)·H-0544-2025·2025-08-20

    Reser's tuna salad containing pickle relish recalled for Listeria monocytogenes risk

    Reser's Tuna Salad in 5 lb foodservice tubs, the version containing pickle relish, is recalled for potential Listeria monocytogenes contamination from recalled breadcrumbs. 108 cases are affected.

    Product
    Reser's Tuna Salad, net wt. 5lb. Foodservice item. Product is packaged in white plastic tub and lid with sticker. Keep Refrigerated. This item contains ingredient Pickle Relish. Distributed by Reser's Fine Foods, Incl, Beaverton, OR. UPC on 5lb. TUB/Lid: 71117 11405 GTIN on Mas
    Category
    Food
    Distribution
    29 states
  • CriticalFDA (Food)·H-0545-2025·2025-08-20

    Molly's Kitchens tuna salad recalled for Listeria risk from recalled breadcrumbs

    Molly's Kitchens Tuna Salad in 5 lb foodservice tubs, distributed by US Foods, is recalled for potential Listeria monocytogenes contamination from recalled Newly Weds Foods breadcrumbs. 1,136 cases are affected.

    Product
    Molly's Kitchens Tuna Salad, item 794599, net wt. 5lb. Foodservice item. Product is packaged in clear printed plastic tub with printed white lid. Keep Refrigerated. Distributed by U.S. Foods, Inc, Rosemont, IL. UPC on 5lb. TUB/Lid: 58108 76447 GTIN on Master Case (2/5# per cas
    Category
    Food
    Distribution
    29 states
  • CriticalFDA (Devices)·Z-2290-2025·2025-08-20

    HeartMate mobile power unit cords recalled over locking feature that may disconnect

    Abbott is recalling 53 HeartMate Mobile Power Unit AC power cords, model 107760, because a misaligned V-Lock may not engage and can allow an unintended disconnect. The FDA classified this as Class I.

    Product
    Brand Name: HeartMate Product Name: Mobile Power Unit, AC Power Cord Model/Catalog Number: 107760 Software Version: N/A Product Description: The HeartMate 3" Left Ventricular Assist System (LVAS) is a set of equipment and materials that together comprise a medical device desi
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0542-2025·2025-08-20

    Sysco foodservice tuna salad recalled over Listeria risk from recalled breadcrumbs

    Sysco Imperial Deluxe Tuna Salad in 5 lb foodservice tubs is recalled for potential Listeria monocytogenes contamination traced to recalled Newly Weds Foods breadcrumbs. 70 cases are affected.

    Product
    Sysco Imperial Deluxe Tuna Salad, Reorder #6526826, net wt. 5lb. Foodservice item. Product is packaged in clear printed plastic tub with printed white lid. Keep Refrigerated. Distributed by Sysco Corporation, Houston, TX 77077 UPC on 5lb. TUB: 74865 79721 GTIN on Master Case (2/
    Category
    Food
    Distribution
    29 states
  • CriticalFDA (Devices)·Z-2181-2025·2025-08-20

    Manual resuscitators recalled because blocked manometer port may disable pressure gauge

    Ambu is recalling 87,156 SPUR II adult resuscitators because the manometer port may be blocked, leaving the manometer non-functional. The FDA classified the action as Class I.

    Product
    Ambu SPUR II Labeled as the following: 1 SPUR II Adult Resuscitator, Adult, Catalog Number: 523211000 2 SPUR II Adult Resuscitator w/Mercury Filter, Adult, Catalog Number: 523611051 3 SPUR II Adult Resuscitator, Single Patient Use Resuscitator, Adult, Catalog Number: 523611057 4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0543-2025·2025-08-20

    Sysco Classic tuna salad recalled over Listeria risk from recalled breadcrumbs

    Sysco Classic Tuna Salad in 5 lb foodservice tubs is recalled for potential Listeria monocytogenes contamination traced to recalled Newly Weds Foods breadcrumbs. 779 cases are affected.

    Product
    Sysco Classic Tuna Salad, Reorder #6724249, net wt. 5lb. Foodservice item. Product is packaged in clear printed plastic tub with printed lid. Keep Refrigerated. Distributed by Sysco Corporation, Houston, TX 77077 UPC on 5lb. Sysco TUB/Lid: 74865 80038 GTIN on Master Case (2/5#
    Category
    Food
    Distribution
    29 states
  • CriticalFDA (Food)·H-0536-2025·2025-08-20

    Colombian fresh cheese recalled over insanitary conditions and possible Listeria contamination

    Quesito El Establo brand Quesito Colombiano, 1 lb, is recalled because it was made and held under insanitary conditions and may be contaminated with Listeria monocytogenes. All product codes are affected.

    Product
    Quesito El Establo brand Spanish Cheese QUESITO COLOMBIANO; INGREDIENTS: Milk, Cheese Cultures, Salt, Vitamins C and D; INGREDIENTES: Leche, Cuajo, Sal, Vitaminas C y D; NET WT. 1 LB.; KEEP REFRIGERATED
    Category
    Food
    Distribution
    1 state
  • CriticalCPSC·25415·2025-07-31

    KidKraft play kitchen hooks caused a toddler's fatal strangulation in Oregon

    KidKraft Farm to Table play kitchens are being recalled because clothing can catch on the accessory hooks. A 23-month-old child died from strangulation and asphyxia in February 2023.

    Product
    KidKraft Farm to Table Model Play Kitchen
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·25393·2025-07-21

    Above-ground pools recalled after nine children drowned using strap footholds

    Above-ground pools 48 inches and taller with compression straps over the vertical support legs are being recalled because the strap can create a foothold. CPSC believes nine children have drowned.

    Product
    48-inch and taller above-ground pools with compression straps running on the outside and over the vertical support legs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0202-2025·2025-07-09

    Harris Teeter Sushi Recalled Over Possible Salmonella Contamination

    Harris Teeter is recalling ZENSHI HANDCRAFTED SUSHI California Rolls due to possible Salmonella contamination from recalled cucumbers used in production.

    Product
    ZENSHI HANDCRAFTED SUSHI California Roll 10pc (Brown Rice) Net Wt. 7.1oz UPC 0 23012 94265 6 & UPC 0 23012 95137 5
    Category
    Food
    Distribution
    8 states
  • CriticalUSDA FSIS·025-2025·2025-07-02

    Kraft Heinz Recalls Oscar Mayer Turkey Bacon Due to Listeria Risk

    Kraft Heinz is recalling Oscar Mayer Turkey Bacon products nationwide due to possible Listeria monocytogenes contamination. No illnesses have been reported.

    Product
    Kraft Heinz Foods Company — Kraft Heinz Foods Company Recalls Turkey Bacon Products Due to Possible Listeria Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1944-2025·2025-06-25

    Dexcom G7 Glucose Receiver recalled due to defective foam or assembly error

    Dexcom, Inc. is recalling Dexcom G7 Glucose Receiver units due to defective foam or assembly error that may cause the speaker to lose contact with the circuit board, preventing audible alerts for low or high blood glucose.

    Product
    Dexcom G7 Glucose Receiver, SKUs (part number): STK-AT-011(MT26403-0), STK-AT-012 (MT26403-0), STK-AT-013 (MT26403-0), STK-GT-001 (MT26403-1), STK-GT-008 (MT26403-5), STK-GT-013 (MT26403-1) , STK-GT-019 (MT26403-4) , STK-GT-100 (MT26403-2), STK-GT-109 (MT26403-2) , STK-GT-113 (
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1946-2025·2025-06-25

    Dexcom One Continuous Glucose Monitoring System Receiver Speaker Defect

    Dexcom, Inc. is recalling Dexcom One Continuous Glucose Monitoring System receivers due to potential defective foam or assembly errors that may cause the speaker to lose contact with internal components, resulting in missed audible alerts for dangerous blood glucose levels.

    Product
    Dexcom One Continuous Glucose Monitoring System, SKUs(Part Number): STK-DO-006 (MT27409-1), STK-DO-013 (MT27409-1), STK-DO-103 (MT27409-2), STK-DO-109 (MT27409-2)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1945-2025·2025-06-25

    Dexcom One+ Continuous Glucose Monitoring System Receiver Speaker Defect

    Dexcom, Inc. is recalling 26,291 units of the Dexcom One+ Continuous Glucose Monitoring System due to defective foam or assembly errors that may prevent audible alerts for low or high blood glucose levels, potentially leading to seizures, loss of consciousness, or death.

    Product
    Dexcom One+ Continuous Glucose Monitoring System, SKU(Part Number): STK-D7-013 (MT28285-1), STK-D7-014 (MT28285-1), STK-D7-103 (MT28285-2)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1814-2025·2025-06-11

    Adult Manual Resuscitator with Medium Adult Mask recalled nationwide

    SunMed Holdings is recalling 11,358 Adult Manual Resuscitators because the filter may be incorrectly attached to the patient port instead of the exhalation port, risking interruption or delay in patient resuscitation that could cause serious harm or death.

    Product
    Adult Manual Resuscitator with Medium Adult Mask, Bag REservoir, Filter, Manometer and 7 ft Oxygen Tubing, REF CPRM1116F
    Category
    Medical Device
    Distribution
    Distributed nationwide