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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1026–1050 of 114834

  • HighCPSC·26748·2026-09-10

    Ricky Joy Recalls Sour Crush Candy Bottles Due to Choking Risk

    Ricky Joy is recalling over 2.3 million Sour Crush Rolling Liquid Candy bottles because the rolling ball can detach, posing a choking hazard.

    Product
    Ricky Joy Sour Crush Rolling Liquid Candy Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·26V585000·2026-09-10

    Forest River Recalls Lone Star Vans Due to Rearview Camera Defect

    Forest River is recalling 2019-2022 Lone Star Vans because cracks in the microprocessor may prevent the rearview camera from displaying properly, increasing crash risk.

    Product
    FOREST RIVER BUS — FOREST RIVER BUS LONE STAR VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26T014000·2026-09-10

    Wheel Pros Recalls 549 Avix TrailTek RT Tires for Incorrect Markings

    Wheel Pros is recalling 549 Avix TrailTek RT tires because the sidewall is incorrectly labeled 'Not for Highway Use,' failing to meet federal safety standards.

    Product
    TIRES:MARKINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1302-2026·2026-09-09

    Ron's Home Style Foods Recalls Pico de Gallo Due to Salmonella Risk

    Ron's Home Style Foods is recalling 5 lb Pico de Gallo containers because jalapenos may be contaminated with Salmonella. The product was distributed in Arkansas, Oklahoma, and Texas.

    Product
    Item # DIPPIC0205RFS Pico de Gallo 5 lb packaged in round plastic container.
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Food)·H-1303-2026·2026-09-09

    Ron's Home Style Foods Recalls Salsa Autentica Due to Salmonella Risk

    Ron's Home Style Foods is recalling 5 lb. containers of Salsa Autentica because the jalapenos used may be contaminated with Salmonella.

    Product
    Item #DIPSAU0205RFS Salsa Autentica 5 lb. packaged in round plastic container.
    Category
    Food
    Distribution
    3 states
  • CriticalFDA (Drugs)·D-0851-2026·2026-09-09

    Optimal Balance Pharmacy Recalls Contaminated Glutathione Injection Vials

    Optimal Balance Pharmacy is recalling 53 vials of Glutathione 200 mg/mL due to bacterial endotoxin contamination.

    Product
    Glutathione 200 mg/mL, 30 mL sterile multidose vial, Each vial contains: Glutathione, Ascorbic Acid, Benzyl Alcohol & sterile water for injection, For IM or IV Injection Use Only, RX only, Optimal Balance Pharmacy, 2204 Cypress Creek Pkwy Suite F, Houston, TX 77090
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-1328-2026·2026-09-09

    Frankie's Organic Plant-Based Puffs Recalled for Undeclared Milk

    Marina Del Rey Foods is recalling Frankie's Organic Plant-Based Puffs Vegan Cheddar due to undeclared milk. The product was sold in Washington, Florida, and South Carolina.

    Product
    Frankie's Organic Plant-Based Puffs Vegan Cheddar, NET WT. 4 oz. (113 g). Product is packaged into flexible plastic bag, UPC 816929000119. Sold wholesale: 12 retail units/ case
    Category
    Food
    Distribution
    6 states
  • SevereFDA (Devices)·Z-3086-2026·2026-09-09

    Fresenius 5008X HD/HDF Blood Tubing Set Recalled for Leak Risk

    Fresenius Medical Care is recalling 18,600 units of 5008X HD/HDF blood tubing sets due to a heightened probability of blood leaks that could cause blood loss and hypovolemia.

    Product
    5008X HD/HDF with CLiC Blood Tubing Set Part number 03-5300-3C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0819-2026·2026-09-09

    Baxter Recalls Vasopressin Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Vasopressin in 0.9% Sodium Chloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    VASOPRESSIN IN 0.9% SODIUM CHLORIDE — VASOPRESSIN IN 0.9% SODIUM CHLORIDE (VASOPRESSIN IN 0.9% SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1309-2026·2026-09-09

    Hampton Grocer Lactation Granola Recalled for Salmonella Contamination Risk

    The Hampton Grocer is recalling Small Batch Lactation Granola due to potential Salmonella contamination. Consumers should stop eating the product and return it for a refund.

    Product
    THE HAMPTON GROCER brand; Lacnola; SMALL BATCH LACTATION GRANOLA, 8oz, stand up pouches; NUTRIENT DENSE INGREDIENTS + MORINGA; SUPPORTS + PROMOTES HEALTHY LACTATION; INGREDIENTS Organic Gluten Free Oats Organic Maple Syrup Organic Pumpkin Seeds Organic Coconut Oil Almond Butter…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3085-2026·2026-09-09

    Fresenius 5008X Blood Tubing Set Recalled for Potential Blood Leak

    Fresenius Medical Care is recalling 5008X HD/HDF Standard Blood Tubing Sets due to a heightened probability of blood leak from the Arterial Alpha Clip connection.

    Product
    5008X HD/HDF Standard Blood Tubing Set Part Number 03-5300-3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3061-2026·2026-09-09

    Medline Eye and Cataract Kits Recalled for Potential Sterility Breach

    Medline is recalling 2,080 eye and cataract preop kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) EYE KIT, Model Number: DYKM2751; 2) EYE KIT, Model Number: DYKM2751A; 3) CATARACT PREOP KIT, Model Number: DYKS1583A; 4) CATARACT PREOP KIT, Model Number: DYKS1583B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3063-2026·2026-09-09

    Medline Blood Draw and Phlebotomy Kits Recalled for Sterility Breach

    Medline is recalling approximately 996,692 blood draw and phlebotomy kits due to potential sterility breaches in the packaging. The defect may expose patients to microbial contamination.

    Product
    Medline Convenience Kits: 1) BLOOD DRAW KIT, Catalog Number: DYLAB1081; 2) WHOLE BLOOD PHLEBOTOMY KIT, Catalog Number: DYNDB3005D; 3) QP KIT, Catalog Number: DYNDB3005F; 4) DOUBLE RED CELL PHLEBOTOMY KIT, Catalog Number: DYNDB3006C; 5) PLATELET PHLEBOTOMY KIT, Catalog…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V576000·2026-09-09

    Ford Recalls 2026 F-150s Due to Rear Axle Bearing Defect

    Ford is recalling 2026 F-150 vehicles because incorrect rear axle tail bearings may cause wheel lock-up or driveshaft separation, increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0809-2026·2026-09-09

    Baxter Recalls Famotidine Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Famotidine Injection due to CGMP deviations. The product was distributed in the US, Puerto Rico, and Chile.

    Product
    FAMOTIDINE — FAMOTIDINE (FAMOTIDINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1308-2026·2026-09-09

    Weis Pasteurized Apple Cider Recalled for High Patulin Levels

    Weis Markets is recalling Pasteurized Apple Cider in Pennsylvania due to high patulin levels. Consumers should stop using the product.

    Product
    Weis (Fresh From the Orchard ) Pasteurized Apple Cider, Contains 100 % Juice, the product comes in the following sizes: Pints, 1/2 Gallon, Gallon, plastic jug. 6 1/2 - gallon jugs per crate.
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0810-2026·2026-09-09

    Baxter Recalls Dexmedetomidine Hydrochloride Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Dexmedetomidine Hydrochloride Injection due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride Injection, 400 mcg per 100 mL (4 mcg/mL) in Galaxy 100 mL Single Dose Container, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, USA, NDC 0338-9557-12.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0821-2026·2026-09-09

    Baxter Recalls Daptomycin Injection Due to Manufacturing Deviations

    Baxter Healthcare is voluntarily recalling specific lots of Daptomycin Injection due to Current Good Manufacturing Practice (CGMP) deviations. The recall covers the US, Puerto Rico, and Chile.

    Product
    Daptomycin, in 0.9% Sodium Chloride Injection, 1,000 mg per 100 mL (10 mg/mL), 1,000 mg total, in 1000 mL Single Dose Container, Rx only, Sterile Nonpyrogenic, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, NDC 0338-0718-12.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3084-2026·2026-09-09

    Fresenius Medical Care Recalls 5008X Standard HD Pre-Flush Blood Tubing Sets

    Fresenius Medical Care is recalling 120 units of 5008X Standard HD Pre-Flush Blood Tubing Sets due to a heightened probability of blood leaks during treatment.

    Product
    5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-3062-2026·2026-09-09

    Medline Convenience Kits Recalled for Potential Sterility Breach

    Medline is recalling 18,290 convenience kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) ORTHO ASPIRATION KIT, Model Number: DYKM1636A; 2) SHOULD BLOCK KIT, Model Number: DYKM1881A; 3) TRIMA KIT, Model Number: DYNDB3077C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26E063000·2026-09-09

    Ford Recalls Battery Energy Control Modules for Software Defect

    Ford is recalling specific Battery Energy Control Modules (BECM) because software errors may cause incorrect charge readings or overheating, increasing crash and fire risks.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY:MANAGEMENT SYSTEM/ENERGY CONTROL MODULE (BMS/BECM):SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1327-2026·2026-09-09

    Ukrop's Bread Pudding Recalled for Metal Fragments

    Ukrop's Homestyle Foods is recalling Bread Pudding with Vanilla Sauce kits due to potential metal fragments. The product was distributed in Kentucky, North Carolina, Virginia, and West Virginia.

    Product
    Bread Pudding with Vanilla Sauce - KIT NET WT 4 LB (1.81Kg) UPC 7 22515 91732 0 Ukrop's Homestyle Foods, LLC Richmond, VA 23230
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-3048-2026·2026-09-09

    Medline Convenience Kits Recalled for Potential Sterility Breach

    Medline is recalling 104 convenience kits due to packaging defects that may compromise sterility, posing a risk of microbial contamination.

    Product
    Medline Convenience Kits: 1) DRAWER 9 CRICOTHYROTOMY KIT, Model Number: ACC010741; 2) KIT ANESTHESIA L&D A- LINE SET, Model Number: DYKMBNDL199A
    Category
    Medical Device
    Distribution
    Distributed nationwide