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.

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

18926–18950 of 39605

  • SevereFDA (Devices)·Z-0343-2018·2018-01-31

    Vyaire Medical Recalls Infant AirLife Humidification Chambers Due to Overflow Risk

    Vyaire Medical is recalling 16,670 Infant AirLife single-limb circuits and humidification chambers because a manufacturing error may cause water to back up into the patient's airway.

    Product
    Infant AirLife single-limb, continuous-flow circuit (Model AH132) containing AirLife Humidification Chamber, Model Number AH290. The AH290 Humidification Chamber and Heated Breathing Circuit Kit(s) operate as part of a system for delivering health and humidified respirator…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0344-2018·2018-01-31

    Vyaire Medical Recalls Infant AirLife Humidification Chamber Due to Overflow Risk

    Vyaire Medical is recalling 16,670 Infant AirLife humidification chambers because a manufacturing error may cause water to overflow into the patient's airway.

    Product
    Infant AirLife Dual-,limb, dual-heat, high-flow circuit (Model AH265) with AirLife Humidification Chamber, Model Number AH290. The AH290 Humidification Chamber and Heated Breathing Circuit Kit(s) operate as part of a system for delivering health and humidified respirator…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0233-2018·2018-01-31

    Pravastatin Sodium Tablets Recalled Due to Foreign Tablet Presence

    International Laboratories, Inc. is recalling Pravastatin Sodium Tablets 10 mg because bottles may contain 20 mg tablets.

    Product
    Pravastatin Sodium Tablets, USP, 10 mg, 30-count bottles, packaged in 12 x 30 tablets for individual patient dispensing per pharmacy dispenser cartons, Rx only, Packaged for: International Laboratories, LLC. St. Petersburg, FL 33710, NDC 54458-927-16.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0345-2018·2018-01-31

    Vyaire Medical Recalls Adult Air-Life Single-Limb Circuits Due to Overflow Risk

    Vyaire Medical is recalling 16,670 units of Adult Air-Life single-limb circuits with Humidification Chambers due to a manufacturing error that may cause water overflow into patient airways.

    Product
    Adult Air-Life single-limb circuit (Model AH202) with AirLife Humidification Chamber, Model Number AH290. The AH290 Humidification Chamber and Heated Breathing Circuit Kit(s) operate as part of a system for delivering health and humidified respirator gasses to patients…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0634-2018·2018-01-31

    Rugby Poly-Vitamin w/ Iron Liquid Recalled for Yeast and B. cepacia

    Pharmatech LLC is recalling Rugby Poly-Vitamin w/ Iron Liquid 50 mL due to the presence of yeast and potential contamination with B. cepacia.

    Product
    Rugby Poly-Vitamin w/ Iron Liquid 50 mL UPC 00536-8530-80
    Category
    Drug
    Distribution
    1 state
  • SevereFDA (Drugs)·D-0234-2018·2018-01-31

    International Laboratories Recalls Pravastatin Sodium Tablets Due to Foreign Tablets

    International Laboratories, Inc. is recalling Pravastatin Sodium Tablets, 20 mg, because bottles may contain 10 mg tablets. Patients should contact their healthcare provider.

    Product
    Pravastatin Sodium Tablets, USP, 20 mg, 30-count bottles, packaged in 12 x 30 tablets for individual patient dispensing per pharmacy dispenser carton, Rx only, Packaged for: International Laboratories, LLC. St. Petersburg, FL 33710, NDC 54458-926-16.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0627-2018·2018-01-31

    Pharmatech Recalls Leader Liquid Vitamin D Supplement for Infants

    Pharmatech LLC is recalling Leader Liquid Vitamin D Supplement for Breastfed Infants due to the presence of yeast and potential contamination with B. cepacia.

    Product
    Leader Liquid Vitamin D Supplement for Breastfed Infants 400 IU 50 mL UPC 096295128628
    Category
    Food
    Distribution
    1 state
  • SevereFDA (Food)·F-0610-2018·2018-01-31

    Fresh-Pak 9oz Slice Apples Recalled for Listeria Contamination

    Fresh Pak, Inc. is recalling 9oz Slice Apples containers potentially contaminated with Listeria monocytogenes. The product was distributed in Michigan, Ohio, and Wisconsin.

    Product
    9oz Slice Apples Container - Fresh-Pak brand. 1 unit per case
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Food)·F-0612-2018·2018-01-31

    Fresh Pak Fruit and Cheese Snacks Recalled for Listeria Risk

    Fresh Pak, Inc. is recalling 7oz fruit and cheese snacks potentially contaminated with Listeria monocytogenes. The products were distributed in Michigan, Ohio, and Wisconsin.

    Product
    7oz Fruit and cheese Snacks - no brand. 1 unit per case
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Devices)·Z-0346-2018·2018-01-31

    Vyaire Medical Recalls AirLife Humidification Chambers Due to Overflow Risk

    Vyaire Medical is recalling 16,670 AirLife Humidification Chambers and circuits because a manufacturing error may cause water to back up into patient airways.

    Product
    Adult AirLife dual-limb, dual-heat circuit (Model AH280) with AirLife Humidification Chamber, Model Number AH290. The AH290 Humidification Chamber and Heated Breathing Circuit Kit(s) operate as part of a system for delivering health and humidified respirator gasses to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0607-2018·2018-01-31

    Fresh Pak Recalls 3lb Bags of Diced Red Apples for Listeria Risk

    Fresh Pak, Inc. is recalling 3lb bags of diced red apples potentially contaminated with Listeria monocytogenes. The product was distributed in Michigan, Ohio, and Wisconsin.

    Product
    3lb Bag Dice Red Apples - no brand. 4 units per case
    Category
    Food
    Distribution
    3 states
  • SevereFDA (Drugs)·D-0575-2018·2018-01-31

    Advanced Pharma Recalls Subpotent Magnesium Sulfate IV Bags

    Advanced Pharma Inc. is recalling 25 bags of Magnesium Sulfate IV solution in Texas due to subpotent product.

    Product
    MAGnesium 2 gm in NS 100 mL Magnesium SULfate (USP) 0.9% Sodium Chloride (USP) in 100 mL Sterile single dose bag, Rx only, Avella of Houston 9265 Katy Dr., Houston, TX ---NDC 42852-907-10
    Category
    Drug
    Distribution
    1 state
  • SevereNHTSA·18V080000·2018-01-30

    Forest River Recalls 2018 Georgetown RVs Due to Wiring Fire Risk

    Forest River is recalling 2018 Georgetown recreational vehicles because undersized wiring may melt and cause a fire. Dealers will install an additional circuit breaker free of charge.

    Product
    FOREST RIVER — FOREST RIVER GEORGETOWN
    Category
    Vehicle
    Distribution
    Distributed nationwide