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.

43676–43700 of 50511

  • HighFDA (Devices)·Z-1166-2013·2013-05-01

    Philips NeuViz Dual CT Scanner Recalled for Pinch Hazard

    Philips and Neusoft are recalling 25 NeuViz Dual CT scanners because user error can cause personnel injuries, including a reported finger pinch.

    Product
    NeuViz Dual series CT Scanner System, Part number (PN): 989605651321. This is a computed X-ray, Tomography system. NeuViz Dual Multi-slice CT Scanner System is intended to produce cross-section images of head and body by computer reconstruction of X-ray transmission data…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V169000·2013-05-01

    Newmar Motorhomes Recalled for Awning Motor Damage Risk

    Newmar is recalling 2013-2014 motorhomes because an awning motor may be damaged during installation, causing the awning to unfurl unexpectedly and increasing injury or crash risk.

    Product
    NEWMAR — NEWMAR CANYON STAR, DUTCH STAR, VENTANA, VENTANA LE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1340-2013·2013-05-01

    All One Multiple Vitamin Powder Recalled for Misleading Dairy Labeling

    All One, Inc. is recalling multiple vitamin powder canisters because the label incorrectly claims 'No Dairy' and 'Certified Vegan' despite containing milk.

    Product
    all One Original Formula Multiple Vitamin & Mineral Powder dietary supplement, 30 Day Supply, 15.9 oz. canisters
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1155-2013·2013-05-01

    Accuray RoboCouch Patient Positioning System Recalled for Defective Gearboxes

    Accuray Incorporated is recalling 16 RoboCouch Patient Positioning Systems because A5 gearboxes responsible for pitch and roll motions may be defective.

    Product
    RoboCouch Patient Positioning System Product Usage: is intended for use in the support and positioning of a patient during radiosurgery and radiotherapy procedures and other medical procedures when precise positioning is required.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1153-2013·2013-05-01

    Nova StatStrip Xpress Glu-Test Strips Recalled for No Result Messages

    Nova Biomedical is recalling specific lots of Nova StatStrip Xpress Glu-Test Strips because they may display a 'no result' message when tested.

    Product
    Nova StatStrip Xpress Glu-Test Strips (Glucose test strips) Catalog # 42214
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V168000·2013-04-30

    Jayco Recalls 2013-2014 Recreational Vehicles Due to Awning Motor Defect

    Jayco is recalling 2,491 recreational vehicles because a damaged awning motor may cause the awning to unfurl unexpectedly, increasing the risk of injury or a crash.

    Product
    JAYCO — JAYCO OCTANE, EAGLE, JAY FLIGHT BUNGALOW, JAY FLIGHT DESTINATION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·13733·2013-04-29

    MTD Recalls Cub Cadet Commercial Mowers Due to Fire Risk

    MTD Products is recalling about 2,100 Cub Cadet 2011 commercial zero turn mowers because fuel can leak from the tank, posing a fire risk.

    Product
    Cub Cadet 2011 Commercial Zero Turn Mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·13V162000·2013-04-26

    Winnebago Recalls 2013-2014 Motorhomes Due to Awning Motor Defect

    Winnebago is recalling specific 2013-2014 motorhomes because an awning motor defect may cause the awning to unfurl unexpectedly, increasing the risk of injury or a crash.

    Product
    ITASCA — ITASCA, WINNEBAGO SUNSTAR, ACCESS, FORZA, SUNOVA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V164000·2013-04-25

    Thor Motor Coach Recalls 2013-2014 Motorhomes for Awning Motor Defect

    Thor Motor Coach is recalling specific 2013-2014 motorhomes because an awning motor defect could cause the awning to unfurl unexpectedly, increasing the risk of injury or a crash.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH CHATEAU, CHALLENGER, FOUR WINDS 5000, HURRICANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13V163000·2013-04-25

    Toyota Recalls FJ Cruiser Vehicles for Excessive Headlamp Brightness

    Toyota is recalling 2007-2013 FJ Cruiser vehicles equipped with specific auxiliary lamp kits because the 55-watt bulbs exceed federal brightness limits, increasing glare and crash risk.

    Product
    TOYOTA — TOYOTA FJ CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·13E021000·2013-04-25

    Cequent Pro Series Translite Bike Racks Recalled for Cradle Tearing

    Cequent is recalling Pro Series Translite Bike Racks because cradles may tear, allowing bikes to fall onto the roadway and create a crash hazard.

    Product
    EQUIPMENT:MECHANICAL:CARRIER/RACK recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13180·2013-04-25

    The Land of Nod Recalls Plush Dollies Due to Choking Hazard

    The Land of Nod is recalling about 2,500 plush handmade baby dolls because their hands can detach, posing a choking hazard to young children.

    Product
    Dollies
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·13181·2013-04-25

    3T Design Recalls Cervélo Bicycles with Aura Pro Handlebars

    3T Design is recalling specific Cervélo bicycles because the handlebar clamps can detach, causing the rider to lose control and potentially be injured.

    Product
    Cervélo Bicycles with Aura Pro Handlebars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1123-2013·2013-04-24

    Advanced Sterilization Products Recalls EVOTECH Endoscope Cleaner Systems

    Advanced Sterilization Products is recalling 273 EVOTECH Endoscope Cleaner & Reprocessor Systems because they did not receive sufficient High Potential (HIPOT) DC voltage testing.

    Product
    EVOTECH Endoscope Cleaner & Reprocessor System, P/N 50004 Designed to automatically clean and high-level disinfect flexible, submersible video or fiber-optic endoscopes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1319-2013·2013-04-24

    Zumbro River Brand Recalls Ideal Protein Ridges Due to Wire Contamination

    Zumbro River Brand is recalling Ideal Protein Sea Salt & Vinegar Ridges because a flour ingredient may contain fine wire pieces.

    Product
    Ideal Protein, Sea Salt & Vinegar Ridges, 7 packets Net WT 1.4 oz (40 g) each. Total net weight 9.9 oz (280 g). Distributed by Laboratories C.O.P Inc., 60 Jean-Proulx St Gatieau QC Canada J8Z 1W1
    Category
    Food
    Distribution
    0 states
  • HighFDA (Devices)·Z-1143-2013·2013-04-24

    Elana Catheter Sizer 2.0 Recalled for Unapproved Distribution

    Elana, Inc. is recalling three Elana Catheter Sizer 2.0 devices because they were distributed in interstate commerce without FDA approval.

    Product
    Elana Catheter Sizer 2.0*** The Elana Catheter Sizer 2.0 is designed to aid the surgeon to assess the bypass graft of the ELANA technique.
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-1137-2013·2013-04-24

    GE Healthcare AW Server Recalled for Patient Data Display Error

    GE Healthcare is recalling AW Server software due to a defect where patient data from one individual may be displayed in the Results Viewer for a different patient.

    Product
    GE Healthcare, AW Server. Product Usage: . AW Server is a medical software system that allows multiple users to remotely access AW applications from compatible computers on a network. The system allows networking, selection, processing and filming of multimodality DICOM…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·13V158000·2013-04-24

    Nissan Recalls 2013 Altima Vehicles Due to Spare Tire Pressure Issues

    Nissan is recalling 2013 Altima vehicles because the spare tires may be significantly over- or under-inflated, which could lead to tire failure and increase the risk of a crash.

    Product
    NISSAN — NISSAN ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1322-2013·2013-04-24

    Tristar Food Wholesale Recalls Dried Medlar for Undeclared Sulfites

    Tristar Food Wholesale Company Inc. is recalling 400g bags of Dried Medlar because the product contains undeclared sulfites.

    Product
    Fructus Lycii (400g). Dried Medlar (Net Wt: 14.11 oz (400G). Ingredients: Dried Medlar. Distributed Exclusively By: Tristar Food Wholesale Company Inc. 115 Amity Street, Jersey City NJ 07304, USA. Product of P.R.C. UPC: 6931653102466
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1131-2013·2013-04-24

    Heritage Labs Path Study Extra Supplies Kit Recalled for Contamination

    Heritage Labs is recalling 25 Path Study Extra Supplies Kits because they contain blood collection tubes with a Lithium Heparin contaminant that could cause erroneous lab results.

    Product
    Heritage Labs Path Study Extra Supplies Kit, Product # A 2376, kit contains 3 zippered plastic bags which hold support supplies for health care providers when treating patients. Bag #3 contains 5 different blood collection tubes (5 each) and 2 different gauge needles--all for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1147-2013·2013-04-24

    Transonic AV Loop Kit Recalled for Blood Leakage Complaints

    Transonic Systems Inc. is recalling HCS3011 and HCS3021 AV Loop Kits due to complaints of blood leakage. The kits are used for cardiovascular status assessment.

    Product
    HCS3011 AV Loop Kit For use with Transonic CO status System Only, -HCS3021 AV Loop Kit For use with Transonic CO status System Only. Product Usage: is indicated for use in patients greater than or equal to 2 years old with arterial and venous lines in the diagnostic…
    Category
    Medical Device
    Distribution
    Distributed nationwide