The Recall Desk

Severity 4 of 5

Severe recalls

The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.

What “severe” means here

Severity 4 (Severe) recalls have a real, documented risk of significant injury, hospitalization, or property damage even if no deaths have been reported. The agency classification is FDA Class II with hospitalization reports, USDA Class I, or a structural vehicle defect. These need attention quickly — not five-alarm urgency but not something to put off. Examples include allergen mislabeling on common allergens for products eaten by children, drug potency out of specification by a margin that could cause measurable harm, and vehicle defects affecting braking or steering.

The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.

14976–15000 of 29202

  • 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 (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 (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
  • SevereNHTSA·18V082000·2018-01-30

    Audi Recalls Vehicles Due to Driver Air Bag Inflator Explosion Risk

    Volkswagen Group of America is recalling specific Audi models because the driver's air bag inflator may explode during deployment, potentially causing serious injury or death.

    Product
    AUDI — AUDI S5 CABRIOLET, S4 CABRIOLET, A3, A4 CABRIOLET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V077000·2018-01-30

    Entegra Recalls Aspire and Insignia Motorhomes Due to Brake Reservoir Defect

    Entegra is recalling 2015-2018 Aspire and Insignia motorhomes because the air brake supply reservoir is undersized, which may reduce braking performance and increase crash risk.

    Product
    ENTEGRA — ENTEGRA INSIGNIA, ASPIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E007000·2018-01-30

    Lippert Components Recalls Ford F53 Chassis for Driveshaft Misalignment

    Lippert Components is recalling specific Ford F53 chassis used in Coachmen and Mirada RVs because a misaligned driveshaft may cause excessive vibration and potential vehicle disablement.

    Product
    STRUCTURE:FRAME AND MEMBERS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V072000·2018-01-29

    Jayco Eagle Travel Trailer Recall for Underrated Safety Chains

    Jayco is recalling 2017-2018 Eagle 333BHOK travel trailers because the safety chains are rated below the vehicle's weight limit, posing a crash risk if the trailer detaches.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V076000·2018-01-29

    Harley-Davidson Recalls ABS Motorcycles Due to Brake Fluid Deposits

    Harley-Davidson is recalling 2008-2011 ABS-equipped motorcycles because brake fluid deposits may cause the ABS valve to stick, reducing braking ability and increasing crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHTP, VRSCF, VRSCDXA, VRSCDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V075000·2018-01-29

    Jayco Recalls 2018 Eagle Travel Trailers Due to Stove Gas Leak Risk

    Jayco is recalling 2018 Eagle travel trailers because the furnace can cause the cooktop flame to go out while gas continues to flow, creating an explosion risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide