The Recall Desk

Severity 3 of 5

High recalls

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

What “high” means here

Severity 3 (High) recalls have a known hazard but no confirmed illness, injury, or property damage in the source text. The risk is theoretical-but-real: a pathogen pre-emptively pulled from shelves before anyone got sick, an allergen mislabeling on an uncommon allergen, a precautionary correction on a device that hasn't yet malfunctioned in the field. Most allergen recalls land here, as do most preventive food recalls based on routine sampling. You should still stop using the product, but you don't need to panic.

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.

42701–42725 of 50511

  • HighNHTSA·13V511000·2013-10-17

    Gulf Stream Travel Trailer Door Lock Recall for Jamming Hazard

    Gulf Stream is recalling 2007-2013 travel trailers equipped with Fastec door locks that may jam, potentially trapping occupants inside the vehicle.

    Product
    GULF STREAM — GULF STREAM RIDGELINE, PRAIRIE SCHOONER, NORTHERN EXPRESS, G FORCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V506000·2013-10-17

    Porsche Recalls 2013-2014 Cayenne Models for Fuel Gauge Inaccuracy

    Porsche is recalling specific 2013-2014 Cayenne vehicles because the fuel gauge may display higher levels than actual, increasing the risk of stalling and crashes.

    Product
    PORSCHE — PORSCHE CAYENNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V505000·2013-10-17

    Toyota Recalls 2013-2014 Models for Windshield Wiper Switch Defect

    Toyota is recalling specific 2013-2014 Corolla, Camry, and Avalon vehicles because a short circuit in the wiper switch may cause the wipers to stop working, reducing visibility.

    Product
    TOYOTA — TOYOTA COROLLA, CAMRY, CAMRY HYBRID, AVALON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V490000·2013-10-17

    KZRV Travel Trailer Recall for Door Lock Jamming Hazard

    KZRV is recalling 2006-2013 travel trailers because a door lock defect may jam the deadbolt, potentially trapping occupants inside.

    Product
    KZRV — KZRV TOWABLE TRAVEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13E057000·2013-10-17

    Keyline Sales Recalls Exterior Doors for Potential Lock Jamming Hazard

    Keyline Sales is recalling exterior doors for cargo and specialty trailers built with Fastec-brand locks. The defect may jam the deadbolt, potentially trapping occupants inside the vehicle.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V513000·2013-10-17

    Outlaw Recalls Horse Trailers with Defective Door Locks

    Outlaw Conversions is recalling 2006-2013 horse trailers with Fastec door locks that may jam, potentially trapping occupants inside.

    Product
    PLATINUM — PLATINUM, 4-STAR, HART HORSE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V509000·2013-10-17

    Outdoors RV Recalls Travel Trailers Due to Door Lock Jamming Risk

    Outdoors RV is recalling specific travel trailers because a defect in the door lock may jam the deadbolt, potentially trapping occupants inside the vehicle.

    Product
    WIND RIVER — WIND RIVER, TIMBER RIDGE, TAMARACK TRAILS TRAVEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V502000·2013-10-17

    Porsche Recalls 2014 Models Due to Passenger Airbag Wiring Defect

    Porsche is recalling certain 2014 Boxster, Cayman, and 911 Carrera vehicles because defective wiring may deactivate the front passenger airbag, increasing injury risk in a crash.

    Product
    PORSCHE — PORSCHE CAYMAN, BOXSTER, 911 CARRERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V491000·2013-10-17

    Harley-Davidson Recalls 2014 Trikes for Brake Fluid Leak Risk

    Harley-Davidson is recalling 2014 Trikes because a machined part may cause brake fluid loss or steering damage, increasing crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON TRIKE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V504000·2013-10-17

    Blue Bird School Bus Recall for Flip Seat Pinch Hazard

    A-Z Bus Sales is recalling 2005-2013 Blue Bird A3RE and D3RE school buses to fix a pinch point hazard in C.E. White flip seats.

    Product
    BLUE BIRD — BLUE BIRD D3RE, A3RE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V508000·2013-10-17

    Big Tex Recalls Utility Trailers Due to Ramp Gate Latch Failure

    Big Tex is recalling 2013-2014 utility trailers because vibrations may cause ramp gate latches to fail, increasing crash risk.

    Product
    BIG TEX — BIG TEX 29SA, 70TV, 70SP, 70LR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0005-2014·2013-10-09

    PhotoMedex Recalls SLT Fiber Delivery Systems Due to Sterility Concerns

    PhotoMedex is recalling 549 units of SLT Fiber Delivery Systems because some may not have been sealed appropriately, compromising the sterile barrier.

    Product
    The product is labeled in part "***Surgical Laser Technologies, Inc. Montgomeryville, PA***SLT Fiber Delivery System***Sterile***Non-Pyrogenic***. The product is packaged in a flexible pouch and includes the following laser surgery accessories - SLT-SSRH 8, Catalog/Product…
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-2318-2013·2013-10-09

    McKesson Horizon Medical Imaging System Recalled for Potential Image Loss

    McKesson Information Solutions LLC is recalling Horizon Medical Imaging software versions 4.6.1 to 11.6. because a server configuration malfunction may cause the loss of digital medical images.

    Product
    McKesson Horizon Medical Imaging (HMI) Radiological Image Processing System, product versions 4.6.1 to 11.6., is a medical image and information management application intended to receive, transmit, store, retrieve, display, print and process digital medical images, digital…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-0001-2014·2013-10-09

    Maquet Recalls Ultima OPCAB Systems Due to Incorrect Blade Labeling

    Maquet Cardiovascular is recalling specific lots of Ultima OPCAB Systems because standard and deep blades were incorrectly labeled, posing a risk during cardiac surgery.

    Product
    Ultima OPCAB System, Sterile, Rx Only, Product Usage: Intended for use during performance of minimally invasive cardiac surgery through a sternotomy incision approach. The ULTIMA Access RailPlatform in combination with the Activator II Drive Mechanism is used to spread the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2292-2013·2013-10-09

    Ebi Solitaire-35 Spinal Fusion Device Recalled for Screw Complaints

    Ebi, LLC is recalling 1,730 units of the Solitaire-35 PEAK Solitaire Anterior Spinal System due to complaints regarding one of the three screws driving through the cage.

    Product
    Solitaire-35 Peek Solitaire Anterior Spinal System. The Solitaire-35 is an intervertebral body fusion device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2301-2013·2013-10-09

    Hologic Selenia Mammography System Software Recall for Image Deletion

    Hologic is recalling 62 Selenia Full Field Digital Mammography Systems because software versions 5.0.x and 5.1.x may delete recent images when the hard drive reaches a 4,000-image threshold.

    Product
    Selenia Full Field Digital Mammography System with software versions 5.0.x and 5.1.x The Selenia Full Field Digital Mammography system generates digital mammography images that can be used for screening and diagnosis of breast cancer. The Selenia Full Field Digital…
    Category
    Medical Device
    Distribution
    19 states
  • HighFDA (Food)·F-1953-2013·2013-10-02

    Snoqualmie Falls Candy Factory Recalls Coconut Brittle Due to Undeclared Milk

    Snoqualmie Falls Candy Factory is recalling Coconut Brittle because the label lists butter and cream but omits milk, a major allergen.

    Product
    Coconut Brittle's is labeled in parts: "***COCONUT BRITTLE***INGREDIENTS: Coconut (preserved with metabisulfate), white sugar, glucose, butter (cream, salt), vanilla, salt***".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1951-2013·2013-10-02

    Snoqualmie Falls Candy Factory Recalls Almond Brittle for Milk Allergen Mislabeling

    Snoqualmie Falls Candy Factory is recalling Almond Brittle because the label lists butter and cream but omits milk, a major allergen. The product was distributed in Washington.

    Product
    Almond Brittle's label is read in parts:"***ALMOND BRITTLE***INGREDIENTS: Sugar, corn syrup, almonds, brown sugar, butter (cream, salt), baking soda, salt. NO PRESERVATIVES ADDED***Net Wt. 8 oz.***www.snofallscandy.com***Toll Free 1-888-636-CANDY***".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2285-2013·2013-10-02

    CareFusion Recalls SmartSite Infusion Sets Due to Tubing Separation Risk

    CareFusion is recalling SmartSite Low Sorbing Infusion Sets because the tubing sleeve may separate below the drip chamber.

    Product
    SmartSite Low Sorbing Infusion Set, Model# 10015048. Intravascular administration set.
    Category
    Medical Device
    Distribution
    Distributed nationwide