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.

24476–24500 of 32189

  • SevereFDA (Food)·F-0507-2015·2014-11-26

    Mt. Olive Kosher Dill Chips Recalled for Potential Glass Fragments

    Mt. Olive Pickle Company is recalling Kosher Dill Chips in 1-gallon glass jars because they may contain glass fragments. Consumers should check production codes and stop using the product.

    Product
    Mt. Olive, Kosher Dill Chips in 1 gallon glass jars, UPC 09300 12841, Mt. Olive, Corner of Cucumber & Vine, P.O. Box 609, Mt Olive, NC 28365-0609.
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Food)·F-0532-2015·2014-11-26

    InHarvest Garden Vegetable Seasoning Recalled for Undeclared Milk

    InHarvest, Inc. is recalling Rio Medley Garden Vegetable Seasoning because it contains milk, which is not declared on the label.

    Product
    Rio Medley/Garden Vegetable 12/36 oz; Product number 12310; Product contains 4 oz. plastic bags of Garden Vegetable Seasoning mix: Ingredients; Maltodextrin, Dehydrated Onion, Dehydrated carrots, Hydrolyzed Corn Protein, Sun-Dried Tomato, Salt, Autolyzed Yeast Extract…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0517-2015·2014-11-26

    Welcome Market Raisin Toast Recalled for Missing Allergen Statements

    Welcome Market Inc is recalling Raisin Toast products because they lack required statements for wheat, soy, and/or milk allergens.

    Product
    Raisin Toast, Net Wt 20 oz.. (1.25 lb) 99 Ranch Market 338 Barber Ln, Milpitas, CA 95035
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Food)·F-0531-2015·2014-11-26

    InHarvest Caviar Medley Garden Vegetable Seasoning Recalled for Undeclared Milk

    InHarvest, Inc. is recalling Caviar Medley Garden Vegetable products because the seasoning mix contains undeclared milk.

    Product
    Caviar Medley/Garden Vegetable 12/36 oz Product number 10610; Caviar Medley/Garden Vegetable 6/26 oz. Product number 10644 Product contains 4 oz. plastic bags of Garden Vegetable Seasoning mix: Ingredients; Maltodextrin, Dehydrated Onion, Dehydrated carrots, Hydrolyzed…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0529-2015·2014-11-26

    Wawa Garden Rotini and Kale Salads Recalled for Undeclared Allergens

    Taylor Farms is recalling Wawa Garden Rotini and Kale & Quinoa Salads due to potential undeclared fish, wheat, and egg allergens.

    Product
    Wawa Garden Rotini Salad with Lite Creamy Caesar Dressing, Net Wt 8 oz. (227 g) Bottom of container - Wawa Kale & Quinoa Salad Distributed by: Wawa, Inc. Wawa, PA 19063 UPC 726191066402
    Category
    Food
    Distribution
    3 states
  • SevereCPSC·15036·2014-11-25

    Goal Zero Sherpa 50 and 120 Battery Packs Recalled for Fire Hazard

    Goal Zero is recalling Sherpa 50 and 120 rechargeable battery packs because they can overheat and catch fire. Consumers should stop using the units and contact the company for a free replacement.

    Product
    Goal Zero Sherpa brand 50 and 120 rechargeable battery packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V751000·2014-11-24

    Capacity Recalls 2014 ISB13 Trucks Due to Fuel Filter Defect

    Capacity is recalling 2014 ISB13 trucks because a fuel filter defect may cause the engine to stall without warning, increasing the risk of a crash.

    Product
    CAPACITY — CAPACITY ISB13
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V750000·2014-11-24

    Harley-Davidson Recalls 2015 Tri-Glide Motorcycles Due to Rear Brake Defect

    Harley-Davidson is recalling 1,560 model year 2015 Tri-Glide motorcycles because a defective rear brake master cylinder piston may cause brake failure and increase crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHTCUTG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V747000·2014-11-24

    Spartan Trucks Recalled for Air Brake Valve Defect

    Spartan is recalling 2013-2015 trucks because damaged air brake valves may reduce braking performance or cause parking brakes to reapply, increasing crash risk.

    Product
    SPARTAN — SPARTAN GLADIATOR, DR, NVS, MM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·082-2014·2014-11-22

    Ranchers Legacy Recalls Ground Beef Products Due To E. Coli O157:H7 Risk

    Ranchers Legacy Meat Co. is recalling 1,200 pounds of ground beef products produced on Nov. 19, 2014, due to possible E. coli O157:H7 contamination.

    Product
    Rancher's US OP LLC — Minnesota Firm Recalls Ground Beef Products Due To Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V746000·2014-11-21

    Terex Recalls 2014 Light Tower AL5 Work Platforms Due to Fuel Tank Defect

    Terex is recalling 84 model year 2014 Light Tower AL5 work platforms because insufficient structural support on the fuel tank could cause it to deform and contact the trailer axle, increasing fire risk.

    Product
    TEREX — TEREX LIGHT TOWER AL5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15032·2014-11-20

    Graco Recalls 11 Stroller Models Due to Fingertip Amputation Hazard

    Graco is recalling 11 stroller models because the folding hinge can pinch a child's finger, causing lacerations or amputations.

    Product
    Aspen, Breeze, Capri, Cirrus, Glider, Kite, LiteRider, Sierra, Solara, Sterling and TravelMate Model Strollers and Travel Systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V738000·2014-11-20

    Mack Trucks Recalls 2015 Pinnacle and Granite Models for Wiring Defect

    Mack Trucks is recalling 2015 Pinnacle and Granite trucks because an incorrectly wired system may fail to control engine speed, increasing the risk of fire.

    Product
    MACK — MACK PINNACLE (CXU), GRANITE (GU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0202-2015·2014-11-19

    Medacta Recalls GMK Intramedullary Extension Rods Due to Breakage Reports

    Medacta is recalling GMK Intramedullary Extension Rods 100 mm after three reported cases of breakage during total knee replacement surgeries.

    Product
    GMK Intramedullary Extension Rod 100 mm is a rod to obtain correct leg alignment during total knee replacement. Rod to obtain correct leg alignment during total knee replacement.
    Category
    Medical Device
    Distribution
    1 state
  • SevereFDA (Food)·F-0475-2015·2014-11-19

    Maine Natural Health Recalls Pure Whey Chocolate for Undeclared Milk

    Maine Natural Health is recalling Pure Whey Chocolate dietary supplements because the labels fail to declare the allergen milk.

    Product
    Pure Whey Chocolate, Dietary Supplement Packaged under the labels: Maine Natural Health and Stronger Faster Healthier Packaged in: 2 lb (32 oz), 10 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0184-2015·2014-11-19

    GE Healthcare Infinia Nuclear Medicine Systems Recalled for Loose Fasteners

    GE Healthcare is recalling Infinia nuclear medicine systems because loose fasteners could cause a portion of the system to fall onto a patient during a scan.

    Product
    GE Healthcare Infinia (including Infinia, Infinia Hawkeye, Infinia II, Infinia II Hawkeye, Infinia II Hawkeye 4, Infinia II VC, Infinia II VC Hawkeye, and Infinia II VC Hawkeye 4) Models: H3000WC, H3000WD, H3000WE, H3000WM, H3000WN, H3000WP, H3000WR, H3000WT, H3000WW, H3000WY…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0493-2015·2014-11-19

    Maine Natural Health Recalls Rejuvenate Vanilla Protein Supplement for Undeclared Milk

    Maine Natural Health, Inc. is recalling Rejuvenate Vanilla Dietary Supplement because it fails to declare the allergen milk. The product was distributed nationwide in 2 lb and 10 oz sizes.

    Product
    Rejuvenate Vanilla Dietary Supplement Packaged under the labels Stronger Faster Healthier: 2 lb (32 oz), and 10 oz sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0487-2015·2014-11-19

    Daily Balance Chocolate Dietary Supplement Recalled for Undeclared Milk Allergen

    Maine Natural Health, Inc. is recalling Daily Balance Chocolate Dietary Supplement because it fails to declare the milk allergen.

    Product
    Daily Balance Chocolate Dietary Supplement Packaged under the labels Stronger Faster Healthier: 2 lb (32 oz), and 10 oz sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0485-2015·2014-11-19

    Maine Natural Health Recalls Endurance In Race Lime Supplement for Undeclared Allergens

    Maine Natural Health, Inc. is recalling Endurance In Race Lime Dietary Supplement because it fails to declare milk and coconut allergens.

    Product
    Endurance In Race Lime Dietary Supplement Packaged under the label Stronger Faster Healthier Pack. Packaged in: 2 lb (32 oz), and 30 gram sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0479-2015·2014-11-19

    Protein Supplement Recalled for Undeclared Milk and Shellfish Allergens

    Maine Natural Health is recalling Recovery Natural protein supplements because they fail to declare milk and shellfish allergens.

    Product
    Recovery Natural (also labeled Post Workout), Dietary Supplement Packaged under the labels: Maine Natural Health and Stronger Faster Healthier Pack Packaged in: 2 lb (32 oz), 10 oz. and 30 gram sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0478-2015·2014-11-19

    Protein Supplement Recalled for Undeclared Milk and Shellfish Allergens

    Maine Natural Health, Inc. is recalling Recovery Chocolate dietary supplements because they fail to declare milk and shellfish allergens.

    Product
    Recovery Chocolate (also labeled Post Workout), Dietary Supplement Packaged under the labels: Maine Natural Health and Stronger Faster Healthier Pack. Packaged in: 2 lb (32 oz), 10 oz. and 30 gram sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0492-2015·2014-11-19

    Maine Natural Health Recalls Fortified Chocolate Supplement for Undeclared Milk

    Maine Natural Health, Inc. is recalling fortified chocolate dietary supplements because they fail to declare the allergen milk. The products are sold nationwide in 2 lb and 10 oz sizes.

    Product
    Fortified Chocolate Dietary Supplement Packaged under the labels Stronger Faster Healthier: 2 lb (32 oz), and 10 oz sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0489-2015·2014-11-19

    Protein supplement recalled for failing to declare milk allergen

    Maine Natural Health, Inc. is recalling Hunger and Weight Vanilla dietary supplements because they fail to declare the milk allergen.

    Product
    Hunger and Weight Vanilla Dietary Supplement Packaged under the labels Stronger Faster Healthier Whey: 2 lb (32 oz), and 10 oz sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0182-2015·2014-11-19

    Philips Allura Xper FD20C Recalled for Faulty Motion Controller

    Philips Medical Systems is recalling two Allura Xper FD20C systems due to a faulty Automatic Motion Controller that may cause hazardous C-arc movement.

    Product
    Philips Medical Systems Allura Xper FD20C with software version R8.2.O System Code: 722035. The Allura Xper FD series are intended for use on human patients to perform: Vascular, cardiovascular and neurovascular imaging applications, including diagnostic, interventional and…
    Category
    Medical Device
    Distribution
    2 states