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.

Filters

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All agenciesFDA (Food)FDA (Drugs)FDA (Devices)USDA FSISCPSCNHTSAEPA

Category

All categoriesFoodDrugMedical DeviceVehicleConsumer Product

Minimum severity

Any3+ (High and above)4+ (High and above)5+ (High and above)

Clear filters

5776–5800 of 89509

  • 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-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
  • SevereFDA (Food)·H-0541-2025·2025-08-20

    Reser's gourmet tuna salad recalled over Listeria in recalled breadcrumbs

    Reser's Gourmet Tuna Salad, 5 lb foodservice tubs, is being recalled because it contains Newly Weds Foods recalled Japanese style breadcrumbs, with potential Listeria monocytogenes contamination. 240 cases affected.

    Product
    Reser's Gourmet Tuna Salad, net wt. 5lb. Foodservice item. Product is packaged in clear printed plastic tub with white lid with white sticker. Keep Refrigerated. Distributed by Reser's Fine Foods, Beaverton, OR. UPC on 5lb. TUB: 71117 85506 GTIN on Master Case (2/5# per case):
    Category
    Food
    Distribution
    29 states
  • SevereFDA (Devices)·Z-2291-2025·2025-08-20

    HeartMate mobile power unit cords may disconnect from a misaligned lock

    HeartMate Mobile Power Units are being recalled because misaligned V-Lock features on the power cords prevent the locking mechanism engaging properly and may cause unintended disconnect. 604 units affected.

    Product
    Brand Name: HeartMate Product Name: Mobile Power Unit Model/Catalog Number: 107754 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 designed to provide
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·028-2025·2025-08-20

    Sabrositos Hondurenos Recalls Meat Products Produced Without Federal Inspection

    Sabrositos Hondurenos, LLC is recalling approximately 32,000 pounds of meat products that were produced without federal inspection and bear false USDA marks.

    Product
    Sabrositos Hondurenos, LLC, Recalls Various Meat Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2227-2025·2025-08-20

    DreamStation Auto CPAP units may hold an incorrect device configuration

    DreamStation Auto CPAP non-continuous ventilators are being recalled because the devices may possess a programming error resulting in an incorrect device configuration. 57 units are affected.

    Product
    DreamStation Auto CPAP. Non-Continuous Ventilator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0473-2025·2025-08-20

    Ready Meals duo tuna salad with crackers recalled over Listeria risk

    Ready Meals Duo Tuna Salad with Crackers is being recalled because of potential contamination with Listeria monocytogenes. The source does not state a quantity.

    Product
    READY MEALS DUO TUNA SALAD W/ CRACKERS
    Category
    Food
    Distribution
    7 states
  • SevereNHTSA·25V533000·2025-08-20

    Mercedes steering coupling bolt may loosen from the steering rack

    Mercedes-Benz is recalling certain 2023-2026 EQE and GLC vehicles because the steering coupling bolt may have been improperly tightened, allowing the coupling to loosen from the steering rack.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQE 500 4MATIC, EQE 350 4MATIC, AMG EQE 53 4MATIC, AMG GLC63 S E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V532000·2025-08-20

    Aston Martin Recalls 2025 Vanquish for Brake Assist Software Defect

    Aston Martin is recalling 2025 Vanquish vehicles because a vacuum pump defect may cause loss of power brake assist, increasing stopping distance and crash risk.

    Product
    ASTON MARTIN — ASTON MARTIN VANQUISH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2228-2025·2025-08-20

    DreamStation Auto BiPAP units may hold an incorrect device configuration

    DreamStation Auto BiPAP non-continuous ventilators are being recalled because the devices may possess a programming error resulting in an incorrect device configuration. 8 units are affected.

    Product
    DreamStation Auto BiPAP. Non-Continuous Ventilator.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-0539-2025·2025-08-20

    Signature Cafe tuna salad recalled over Listeria in recalled breadcrumbs

    Signature Cafe Premium Tuna Salad, 3 lb foodservice tubs, is being recalled because it contains Newly Weds Foods recalled Japanese style breadcrumbs, with potential Listeria monocytogenes contamination. 165 cases affected.

    Product
    Signature Cafe Premium Tuna Salad, net wt. 3lb (48oz). Foodservice item to be used by deli. Product is packaged in clear plastic tub with printed white lid. Keep Refrigerated. Distributed by Lucerne Foods, PO Box 99, Pleasanton, CA. UPC on 3lb. TUB: 71117 06036 GTIN on Mast
    Category
    Food
    Distribution
    29 states
  • HighFDA (Drugs)·D-0582-2025·2025-08-20

    Metoprolol tartrate 100 mg tablets exceed the nitrosamine daily intake level

    Metoprolol Tartrate Tablets USP 100 mg distributed by Westminster Pharmaceuticals are being recalled because N-nitroso-metoprolol was present above the established Acceptable Daily Intake level. 4,456 bottles affected.

    Product
    Metoprolol Tartrate Tablets, USP, 100 mg, 1000 Tablets, Rx Only, Manufactured by: Renata PLC (General Plant -2), Noyapara, Bhawal Mirzapur, Rajendrapur, Gazipur, 1700 Bangladesh, Distributed by: Westminster Pharmaceuticals, LLC, Nashville, TN 37217, NDC 69367-355-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0463-2025·2025-08-20

    Coconut con crema 6-pack paletas recalled over undeclared milk in cream

    La Michoacana Coconut Con Crema 6-Pack Paletas, 16.5 oz, are recalled nationwide because the label lists cream but does not declare milk as its source. 47,065 units are affected.

    Product
    La Michoacana Coconut Con Crema 6-Pack Paleta 16.5oz UPC: 7-67778-00101-0
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0494-2025·2025-08-20

    Green Reviver juice distributed unpasteurized in violation of juice HACCP rules

    Green Reviver Juice is being recalled because the firm manufactured and distributed unpasteurized juice products to retailers in violation of the Juice HACCP regulations. 1,932 bags are affected.

    Product
    FG60007 Green Reviver Juice - point of service product
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-2284-2025·2025-08-20

    Kittner roll gauze with tail recalled over contamination and incorrect pack quantity

    Carefree Surgical Specialties Kittner Roll Gauze + Tail, catalog 15506/25 lot 1607, is recalled for biological foreign matter that could compromise sterility and for incorrect gauze counts. 65 units are affected.

    Product
    Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner Roll Gauze + Tail Medium 4 Long X-Ray Detectable 5pk 25pk/CS Roll Gauzes Model/Catalog Number: 15506/25 Product Description: Robotic/Laparoscopy Kittner Roll Gauze + Tail Medium 4 Long X-Ray
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0497-2025·2025-08-20

    Tarantino lemon pepper seasoning may contain small metal fragments

    Tarantino Lemon Pepper Seasoning in 50 lb units is being recalled because it may contain small metal fragments from a contaminated onion powder ingredient. 731 pounds in total are affected.

    Product
    Lemon Pepper Seasoning (Tarantino) NET WT: 50 lb UPC (QST# 6402)
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·H-0470-2025·2025-08-20

    Helados Mexico choco dipped paletas list cream without declaring milk

    Helados Mexico Choco Dipped Minis Variety Paletas 12-count are being recalled because the label includes the ingredient cream but does not include milk as the source. 70,044 units affected.

    Product
    Helados Mexico Choco Dipped Minis Variety Paletas 12-Count 18oz UPC: 6-82082-41215-7
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0581-2025·2025-08-20

    Metoprolol tartrate tablets recalled for nitrosamine above acceptable daily intake level

    Metoprolol Tartrate Tablets USP, 50 mg, distributed by Westminster Pharmaceuticals, are recalled nationwide after N-nitroso-metoprolol was found above the established Acceptable Daily Intake. 16,672 bottles are affected.

    Product
    Metoprolol Tartrate Tablets, USP, 50 mg, 1000 Tablets, Rx Only, Manufactured by: Renata PLC (General Plant -2), Noyapara, Bhawal Mirzapur, Rajendrapur, Gazipur, 1700 Bangladesh, Distributed by: Westminster Pharmaceuticals, LLC, Nashville, TN 37217, NDC 69367-354-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0451-2025·2025-08-20

    Classic curry Indian sauce recalled over potential metal pieces in product

    Sukhi's Classic Curry Indian Curry Sauce, 3 oz, is recalled for potential contamination with metal pieces. The recall covers 1,125 pounds distributed across more than 25 states.

    Product
    Sukhi's, CLASSIC CURRY INDIAN CURRY SAUCE, NET WT 3 OZ., UPC 7-67226-00165-4, DISTRIBUTED BY: SUKHI'S GOURMET INDIAN FOODS 25823 CLAWITER ROAD, HAYWARD, CA 94545 USA
    Category
    Food
    Distribution
    33 states
  • HighFDA (Devices)·Z-2283-2025·2025-08-20

    Kittner gauze rolls had biological foreign matter and wrong pack quantity

    Carefree Surgical Specialties Robotic/Laparoscopy Kittner Rolls Gauze is being recalled for product contamination with biological foreign matter that could compromise sterility, and an incorrect quantity of gauze in sterile packaging.

    Product
    Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner Rolls Gauze Medium 4 Long X-Ray Detectable 5/pk 25pk/CS Model/Catalog Number: 15505/25 Product Description: Robotic/Laparoscopy Kittner Rolls Gauze Medium 4 Long X-Ray Detectable 5/pk 25pk/
    Category
    Medical Device
    Distribution
    Distributed nationwide