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.

28076–28100 of 32246

  • SevereNHTSA·13V253000·2013-06-21

    Elkhart Coach Shuttle Bus Recall for Wheelchair Lift Fire Risk

    Elkhart Coach is recalling 2006-2012 shuttle buses because a wheelchair lift cable may cause a short circuit and fire.

    Product
    ELKHART COACH — ELKHART COACH SHUTTLE BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V258000·2013-06-21

    Vermeer Recalls 2012-2013 R9X12T Trailers Due to Air Brake Defect

    Vermeer is recalling 2012-2013 R9X12T trailers because an incorrectly installed air-brake booster valve may increase stopping distances, raising the risk of a crash.

    Product
    VERMEER — VERMEER R9X12T
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V261000·2013-06-21

    Mobility Works Recalls Ford E-Series Vans with Wheelchair Lift Fire Risk

    Mobility Works is recalling 2006-2012 Ford E-150, E-250, and E-350 vans equipped with specific wheelchair lifts due to a potential fire hazard from cable contact.

    Product
    FORD — FORD E-350, E-250, E-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13E035000·2013-06-21

    Sutrak HVAC Systems Recalled for Potential Fire Risk in DART Buses

    Sutrak USA is recalling HVAC systems used in DART 39000 buses because a fuse holder defect may allow voltage spikes that damage electrical components and cause a fire.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V255000·2013-06-20

    Mitsubishi Recalls 2011 Outlander Sport for Glass Roof Adhesion Defect

    Mitsubishi is recalling 2011 Outlander Sport vehicles because the panoramic glass roof may have been installed without primer, potentially allowing it to detach.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V254000·2013-06-20

    NABI Transit Buses Recalled for HVAC Electrical Fire Risk

    North American Bus Industries is recalling 2012-2013 transit buses due to a fuse holder defect that may cause voltage spikes and electrical fires.

    Product
    NABI — NABI 40LFW, 31LFW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-597-2013·2013-06-19

    Sandoz Recalls Cefazolin Injection Vials Due to Sterility Concerns

    Sandoz Inc. is recalling Cefazolin for Injection, USP 1 gm vials, lot DB2208, due to a lack of assurance of sterility caused by broken or cracked vials.

    Product
    Cefazolin, injection, 1 gram per vial, 25 vials per box, sterile, Rx only, single-use vial, Manufactured in Austria by Sandoz GmbH for Sandoz, Inc. Princeton, NJ 08540, NDC 00781-3451-70 (vial), NDC 00781-3451-96 (box)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1523-2013·2013-06-19

    XYMOGEN Artriphen Recalled for Undeclared Soy and Milk Allergens

    XYMOGEN Artriphen joint supplement is being recalled because the label fails to declare soy and milk, posing a risk to allergic consumers.

    Product
    XYMOGEN EP Exclusive Patented Dietary Supplement Artriphen Clinically Tested to Support Healthy Joint Function, 90 and 180 capsule bottles
    Category
    Food
    Distribution
    42 states
  • SevereFDA (Food)·F-1525-2013·2013-06-19

    Uncle Eddies Vegan Oatmeal Chocolate Cookies Recalled for Undeclared Walnuts

    International Desserts is recalling Uncle Eddies Vegan Oatmeal Chocolate Cookies because they may contain undeclared walnuts.

    Product
    Uncle Eddies Vegan Oatmeal Chocolate Cookies, 12 oz. One shipping carton/case consists of 12bags. Product labeling reads in part:"uncle Eddies vegan oatmeal chocolate-chip cookies***net wt. 12 oz (340g)***MFG BY:INTERNATIONAL DESSERTS GLENDALE, CA 91203***(818)…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1519-2013·2013-06-19

    Trophy Nut and Nut Barrel Red Pistachio Tubes Recalled for Salmonella Risk

    Trophy Nut Co Inc is recalling specific Red Pistachio Tubes because they were made with pistachios potentially contaminated with Salmonella.

    Product
    Trophy Nut Brand 1.5 oz. Red Pistachio Tube and Nut Barrel Brand 1.25 oz. Red Pistachio Tube.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V259000·2013-06-19

    Isuzu, Chevrolet, and GMC Trucks Recalled for Oil Pan Heater Fire Risk

    Isuzu is recalling specific 2001-2013 trucks because debris on the oil pan heater extension cord can cause overheating and fire.

    Product
    CHEVROLET — CHEVROLET, GMC, ISUZU W-SERIES, N-SERIES, FRR, WT5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1528-2013·2013-06-19

    Blessing Seafood Recalls Wild White EZ Peel Shrimp for Undeclared Sulfites

    Blessing Seafood is voluntarily recalling specific lots of Wild White EZ Peel Shrimp due to undeclared sulfites. The product was sold at Hy-Vee stores and one fish market.

    Product
    Blessing Brand Wild White EZ Peel Shrimp, 16/20 CT. 4 x 5 lbs cartons. The product is bagged in 5 lbs clear plastic bags, the only label iss on the master carton. The product is sold in a seafood retail case. Product labeled as:"WILD WHITE EZ PEEL SHRIMP 16/20 CT WILD…
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-1526-2013·2013-06-19

    Dairy Fresh Recalls IGA Ice Cream for Undeclared Allergens

    Dairy Fresh LLC is recalling IGA Brand Vanilla & Chocolate Ice Cream because it contains undeclared almonds, coconut, and soy lecithin.

    Product
    IGA Brand Vanilla & Chocolate Ice Cream, 1.75 Quart
    Category
    Food
    Distribution
    9 states
  • SevereFDA (Food)·F-1532-2013·2013-06-19

    Hazelnut Growers of Oregon Recalls In-Shell Hazelnuts for Salmonella Risk

    Hazelnut Growers of Oregon is recalling bulk in-shell hazelnuts due to potential Salmonella contamination. The product was distributed in Canada.

    Product
    Jumbo Barcelona in-shell hazelnuts and Large Barcelona in-shell hazelnuts, raw, Hazelnut Growers of Oregon Brand, package in bulk 50 pound screen-printed fabric sack. The product is labeled in parts: "***IN SHELL HAZELNUTS***HAZELNUT GROWERS OF OREGON***OREGON U.S. NO.…
    Category
    Food
    Distribution
    0 states
  • SevereFDA (Food)·F-1527-2013·2013-06-19

    Southwest Ice Cream Specialties Recalls Ice Cream for Undeclared Allergens

    Southwest Ice Cream Specialties is recalling 1,524 cartons of ice cream because the product may contain undeclared pecan, soy, and/or wheat allergens.

    Product
    "Shurfine CREAMERY SELECT PREMIUM ICE CREAM Dulce de Leche Caramel Swirled in Caramel Ice Cream KEEP FROZEN 1.75 QUARTS (1.66L)" is displayed on the carton's label in error. The lid bears the label "Shurfine CREAMERY SELECT PREMIUM ICE CREAM Praline Pecan KEEP FROZEN 1.75…
    Category
    Food
    Distribution
    7 states
  • SevereFDA (Food)·F-1520-2013·2013-06-19

    Trophy Nut Pistachios Recalled Due to Salmonella Contamination Risk

    Trophy Nut Co Inc is recalling 6 oz. natural pistachios because they were made with pistachios that may be contaminated with Salmonella.

    Product
    Trophy Nut Brand 6 oz. natural pistachios
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·13221·2013-06-19

    Kolcraft Recalls Jeep Liberty Strollers Due to Wheel Projectile Hazard

    Kolcraft is recalling Jeep Liberty strollers because tire inner tubes can rupture, causing wheel rims to fly off as projectiles. The defect has resulted in 18 reported injuries.

    Product
    Jeep Liberty Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1505-2013·2013-06-19

    Pure Herbs Protein Extract Recalled for Undeclared Milk and Soy Allergens

    Pure Herbs, Ltd. is recalling Natural Herbal Extracts Protein Dietary Supplement bottles because they contain undeclared milk and soy allergens, posing a risk of serious allergic reactions.

    Product
    Pure Herbs, Ltd. Natural Herbal Extracts Protein Dietary Supplement.120mL/4 fl. oz. bottle; 30mL/1 fl.oz bottle.
    Category
    Food
    Distribution
    0 states
  • SevereNHTSA·13E034000·2013-06-19

    Ohlins Steering Dampers Recalled for Cracking Bracket Risk

    Ohlins is recalling steering dampers for BMW motorcycles because an incorrectly machined bracket may crack, potentially causing steering to lock and leading to injury or a crash.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1436-2013·2013-06-19

    Endologix AFX Introducer System Recalled for Dilator Breakage

    Endologix Inc. is voluntarily recalling 53 units of the AFX Introducer System due to reports of dilator breakage during clinical procedures.

    Product
    Brand Name: AFX" Introducer System, Model Number S17-45. Lot Numbers: 1079840, 1079843, 1079844, 1079845. Product Usage: The AFX Introducer System is intended for use to facilitate the introduction of catheters and other medical devices into the vasculature and to minimize…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V251000·2013-06-18

    Forest River Recalls 2014 Motorhomes Due to Battery Short Circuit Risk

    Forest River is recalling 289 model year 2014 Sunseeker, Forester, Lexington, and Solera motorhomes because a battery isolation manager short circuit could cause smoke or fire.

    Product
    FOREST RIVER — FOREST RIVER SUNSEEKER, SOLERA, LEXINGTON, FORESTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·13V247000·2013-06-13

    NABI Transit Buses Recalled for Loose Air Brake Pedal Mounting

    North American Bus Industries is recalling 2003-2013 45CLFW and 2013 40CLFW transit buses because the air brake pedal mounting may become loose, increasing crash risk.

    Product
    NABI — NABI 45CLFW, 40CLFW
    Category
    Vehicle
    Distribution
    Distributed nationwide