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.

16476–16500 of 29206

  • SevereFDA (Food)·F-1555-2017·2017-03-08

    Papa John's Recalls Pepper Jack Cheese Half Moons for Listeria Risk

    Papa John's Salads & Produce is voluntarily recalling Pepper Jack Cheese Half Moons due to possible Listeria monocytogenes contamination.

    Product
    Pepper Jack Cheese Half Moons, 15pkgs/case UPC 78279600895
    Category
    Food
    Distribution
    2 states
  • SevereFDA (Drugs)·D-0491-2017·2017-03-08

    Mylan Recalls Glipizide Extended-Release Tablets Due to Foreign Tablet Presence

    Mylan Pharmaceuticals is recalling 1,338 bottles of Glipizide 5 mg Extended-Release Tablets because they may contain 10 mg tablets.

    Product
    glipiZIDE Extended-Release Tablets, 5 mg, 1000 count bottles, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV --- NDC 0378-0342-10
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1252-2017·2017-03-08

    Olympus Uretero-reno Videoscope Recall Due to Insertion Tube Breakage

    Olympus is recalling URF-V2 and URF-V2R endoscopes because the insertion tube bending section may break during surgery, causing tissue trauma.

    Product
    Uretero-reno videoscope URF-V2 and URF-V2R endoscope and accessories The URF-V2/V2R endoscopes are intended for use in endoscopic diagnosis and treatment within the ureter and kidney.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V149000·2017-03-07

    Mercedes-Benz and Freightliner Sprinter Vehicles Recalled for Driveshaft Welding Defect

    Daimler Vans USA is recalling 2016 Mercedes-Benz and Freightliner Sprinter 2500 and 3500 vehicles because a driveshaft bracket may not be properly welded, posing a fire risk in a crash.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 2500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V140000·2017-03-03

    REV Recalls Motorhomes Due to Improperly Secured Fuel Pump and Filter

    REV Recreation Group is recalling specific 2015-2017 Fleetwood and Holiday Rambler motorhomes because an improperly secured fuel pump or filter may leak fuel, increasing the risk of fire or explosion.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD VACATIONER XE, STORM, ADMIRAL XE, FLAIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V133000·2017-03-02

    Porsche Recalls Macan Models Due to Passenger Air Bag Sensor Defect

    Porsche is recalling 2015-2017 Macan models because a faulty sensor may deactivate the front passenger air bag, increasing injury risk in a crash.

    Product
    PORSCHE — PORSCHE MACAN S, MACAN TURBO, MACAN GTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V138000·2017-03-02

    BMW Recalls X5 and X6 Models for Driveshaft Wear Risk

    BMW is recalling 2011-2014 X5 and X6 vehicles because water and debris may cause the front driveshaft universal joint to fail, potentially affecting traction and increasing crash risk.

    Product
    BMW — BMW X5, X6, X6 ACTIVEHYBRID SAC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17102·2017-03-02

    Polaris Recalls RZR and GENERAL Off-Highway Vehicles for Fire Hazards

    Polaris is recalling about 13,500 RZR and GENERAL off-highway vehicles due to engine misfires and brake issues that can cause fires and burns.

    Product
    Polaris recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1492-2017·2017-03-01

    Hy-Vee Holiday Candy Recalled Due to Potential Salmonella Contamination

    Hy-Vee Stores Inc. is recalling Holiday Candy in various plastic tray sizes because an ingredient may be contaminated with Salmonella.

    Product
    Holiday Candy packaged in a 10"/16oz. (UPC 026139100000), 12" /32 oz. (UPC 026139300000), 16"/48 oz. (UPC 026139500000), and 18"/64 oz. (UPC 026139700000) plastic tray containers for retail sale, labeled with Hy-Vee scale ticket. The product was labeled HyVee West Des Moines…
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-1495-2017·2017-03-01

    Palmer's Candies Chocolate Almond Bark Recalled for Salmonella Risk

    Palmer and Company is recalling specific chocolate almond bark products because an ingredient may be contaminated with Salmonella.

    Product
    A) Palmer's Candies Chocolate Almond Bark , NET WT 9 OZ (255 g) packaged in plastic clamshell container, UPC 77232-17250; B) Publix Bakery Almond Bark with Cocoa, NET WT 10 OZ (283 g), packaged in paper bags, UPC 77232-22691; C) Palmer's Candies Chocolate Almond Bark, 10 lbs.…
    Category
    Food
    Distribution
    34 states
  • SevereNHTSA·17V130000·2017-03-01

    New Flyer Transit Buses Recalled for Front Axle Beam Cracks

    New Flyer is recalling 2,357 transit buses from 2005-2007 because front axle beams may crack and fail, risking loss of vehicle control.

    Product
    NEW FLYER — NEW FLYER GE40LF, D60LFR, D60LF, C35LF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1497-2017·2017-03-01

    Palmer's Candies Cookies & Cream Bark Recalled for Salmonella Risk

    Palmer and Company is recalling Palmer's Candies Cookies & Cream Bark because an ingredient may be contaminated with Salmonella.

    Product
    Palmer's Candies Cookies & Cream Bark, NET WT 9 OZ (255 g) packaged in plastic clamshell container, UPC Code 77232-17254
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Drugs)·D-0475-2017·2017-03-01

    Apotex Recalls Cyclosporine Capsules Due to Impurity Failures

    Apotex Inc. is recalling 19,584 bottles of Cyclosporine Capsules, USP, 100 mg, because the product failed impurity specifications.

    Product
    CYCLOSPORINE — CYCLOSPORINE (CYCLOSPORINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1488-2017·2017-03-01

    Hy-Vee Chocolate Almond Pretzels Recalled for Salmonella Risk

    Hy-Vee is recalling chocolate almond pretzels because an ingredient may be contaminated with Salmonella. The product was sold in eight states.

    Product
    Chocolate almond pretzels packaged in 4 oz. (UPC 026131900000) and 12 oz. (UPC 026131800000) plastic tray containers for retail sale, labeled with Hy-Vee scale ticket. The product was labeled HyVee West Des Moines, IA.
    Category
    Food
    Distribution
    8 states
  • SevereUSDA FSIS·018-2017·2017-03-01

    Procesadora La Hacienda Recalls Raw Meat Products Due to Undeclared Allergens

    Procesadora La Hacienda is recalling raw seasoned meat products because they contain undeclared wheat and milk allergens. No adverse reactions have been reported.

    Product
    Procesadora La Hacienda, Inc. — Procesadora La Hacienda, Inc. Recalls Meat Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    1 state
  • SevereNHTSA·17V131000·2017-03-01

    REV Recalls 2017 Ambulances Due to Rear Brake Bolt Torque Issue

    REV Ambulance Group is recalling 69 specific 2017 Type I ambulances because overtightened rear brake bolts may cause loss of braking power.

    Product
    MARQUE — MARQUE, FRONTLINE, WHEELED COACH TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1165-2017·2017-03-01

    Biomet Recalls Oxford Partial Knee Trial Trays Due to Material Inclusions

    Biomet U.K., Ltd. is recalling Oxford Partial Knee System trial trays due to potential alumina inclusions that could cause cracking and separation.

    Product
    Oxford Partial Knee System Right Medial Tibial Trial Tray Size C Oxford Partial Knee System Left Medial Tibial Trial Tray Size C
    Category
    Medical Device
    Distribution
    14 states
  • SevereFDA (Food)·F-1510-2017·2017-03-01

    Palmer's Chocolatey Pretzels Recalled for Potential Salmonella Contamination

    Palmer and Company is recalling 198 cases of Palmer's Candies Chocolatey Pretzels because an ingredient may be contaminated with Salmonella.

    Product
    Palmer's Candies Chocolatey Pretzels NET WT 28 lbs (12.7 kg), packaged cardboard boxes, UPC 77232-10798
    Category
    Food
    Distribution
    34 states