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.

38601–38625 of 50506

  • HighFDA (Devices)·Z-1657-2015·2015-06-03

    Philips Ingenuity CT Recall for Unexpected Patient Couch Descent

    Philips is recalling 153 Ingenuity CT systems in China because the patient couch unexpectedly descended to its lowest point during an exam.

    Product
    Ingenuity CT. Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-2337-2015·2015-06-03

    Regency Group Recalls Taco Seasoning No Salt Due to Gluten Contamination

    Regency Group, Inc. is recalling Taco Seasoning No Salt because it is contaminated with gluten (wheat) and the label does not declare wheat.

    Product
    Taco Seasoning No Salt, stock code 03455, packaged in 1 lb., 2 lbs., 3 lbs., or 5 lbs., container. The UPC is 0 23605 03455 3
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1687-2015·2015-06-03

    Terumo Advanced Perfusion System 1 Recalled for Power Loss Risk

    Terumo is recalling 1,713 Advanced Perfusion System 1 units worldwide due to a risk of losing system power during critical medical procedures.

    Product
    100/120V AC, Advanced Perfusion System Platform (APS) The Terumo¿ Advanced Perfusion System 1 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1675-2015·2015-06-03

    Mindray Recalls Panorama Patient Monitoring Network Due to Software Anomaly

    Mindray is recalling four Panorama Patient Monitoring Network units due to a software anomaly that prevents arrhythmia alarms from displaying on the Panorama system after a restart.

    Product
    Panorama Patient Monitoring Network, Multi- Parameter Patient Monitor (with Arrhythmia Detection and Alarm. Part number 0998-00-0708-01. The Panorama Network includes the Panorama Telemetry System, which acquires and monitors physiological data for ambulating patients…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V336000·2015-06-02

    Airstream Interstate Motorhomes Recalled for Screen Door Exit Hazard

    Airstream is recalling 2015-2016 Interstate NCV3 B motorhomes because the screen door may prevent occupants from opening the sliding door to exit in an emergency.

    Product
    AIRSTREAM — AIRSTREAM INTERSTATE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V338000·2015-06-02

    Mitsubishi, Chrysler, and Dodge Recall Vehicles for Sun Visor Airbag Hazard

    Mitsubishi, Chrysler, and Dodge are recalling specific 2000-2005 vehicles because the passenger sun visor may detach during airbag deployment, increasing injury risk.

    Product
    MITSUBISHI — MITSUBISHI, CHRYSLER, DODGE ECLIPSE SPYDER, SEBRING, STRATUS, ECLIPSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V340000·2015-06-02

    Ford Recalls 2011-2013 Vehicles for Electric Power Steering Defect

    Ford is recalling specific 2011-2013 Ford, Lincoln, and Mercury vehicles because the electric power steering assist system may shut down, increasing crash risk.

    Product
    LINCOLN — LINCOLN, FORD, MERCURY MKZ, FUSION, MILAN, TAURUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15154·2015-06-02

    ORTOVOX S1+ Avalanche Transceiver Recalled for Signal Failure Risk

    CPSC recalls about 3,000 ORTOVOX S1+ avalanche transceivers because they may fail to transmit a signal during emergencies. Consumers should stop using them and return them for repair.

    Product
    ORTOVOX S1+ Avalanche Transceiver
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V333000·2015-06-01

    New Flyer Transit Bus Recall for Door Software Defect

    New Flyer is recalling specific transit buses because a software defect may cause rear doors to open while the bus is moving.

    Product
    NEW FLYER — NEW FLYER XDE35, XN40, XN60, C40LFR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V326000·2015-05-29

    Genie TZ-34/20 Trailers Recalled for Outrigger Drift Risk

    Genie is recalling 2015 TZ-34/20 trailers because out-of-specification cylinders may cause outriggers to drift, increasing the risk of tip-over and injury.

    Product
    GENIE — GENIE TZ-34/20
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15151·2015-05-28

    Mason Jar Night Light Recalled Due to Burn Hazard

    Nantucket Distributing is recalling Mason Jar Night Lights because the plastic base can melt, posing a burn hazard. No injuries have been reported.

    Product
    Mason Jar Night Light
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15152·2015-05-28

    GT Fury Mountain Bicycles Recalled Due to Front Wheel Hub Failure Risk

    Cycling Sports Group is recalling 2015 GT Fury Elite and Expert downhill mountain bicycles because the front wheel hub can break, causing disc brake failure and crash hazards.

    Product
    GT downhill mountain bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2311-2015·2015-05-27

    Bridge City Baking Recalls Gluten-Free Cherry Crumble Pies for Undeclared Milk

    Bridge City Baking LLC is recalling frozen gluten-free Cherry Crumble Pies because butter is listed without its sub-ingredient, milk.

    Product
    BRIDGE CITY Baking gluten free Cherry Crumble Pie. This product is frozen ready to bake. Net Wt 24oz UPC 0 91037 54455 1
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-2300-2015·2015-05-27

    Alpine Bistro 7-Layer Bar Recalled for Undeclared Wheat Allergen

    Alpine Bistro & Bakery Company is recalling 7-Layer Bars because they contain wheat but are labeled as Graham crackers without declaring the wheat allergen.

    Product
    7 -Layer Bar, 7-ounce(200 gram) flexible plastic wrap with adhesive-backed label.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1631-2015·2015-05-27

    Philips EPIQ 5 Ultrasound System Recalled for Body Surface Area Calculation Error

    Philips is recalling EPIQ 5 Ultrasound Systems due to a unit conversion error that may cause incorrect Body Surface Area calculations when using Metric settings.

    Product
    EPIQ 5 Ultrasound System versions 1.3.2 or lower, WITHOUT the Pediatric Cardiology option, Model: EPIQ 5G, EPIC 5C, EPIQ 5W.Catalog Number: 795204 / 795205. Part Number: 989605408541 With 453561736761 (1.1) 453561750041 (1.1.1) 453561753651 (1.1.2) 453561772231 (1.2)…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1639-2015·2015-05-27

    Richard Allan Scientific Recalls Mucolytic Agent Due to Fungal Contamination

    Richard Allan Scientific is recalling Mucolytic Agent and Mucolexx after a customer complaint reported fungal contamination in two lots of Mucolexx.

    Product
    Mucolytic Agent 1 pint/473 ml; 1 gallon/3.8 l Product Usage: A mucoliquefying preservative designed for use in the preparation of mucoid cytology specimens. Mucolexx & Mucolytic Agent liquefies mucus and allows for optimal cytologic diagnostic results.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1628-2015·2015-05-27

    Baxter ABACUS Software Recalled for Potential TPN Formula Loading Errors

    Baxter is recalling ABACUS SE and ME software because it may load incorrect total parenteral nutrition formulas when duplicate order numbers are used.

    Product
    ABACUS SE (Single-Workstation Edition) and ABACUS ME (Multi-Workstation Edition) Product Usage: The ABACUS Software is a Windows-based order entry software application for comprehensive total parenteral nutrition (TPN) calculations and label printing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1642-2015·2015-05-27

    DeRoyal Specimen Retrieval Bags Recalled for Tearing During Use

    DeRoyal Industries is recalling 5,359 Medium Specimen Retrieval Bags because they may tear or come apart during laparoscopic procedures.

    Product
    DeRoyal(R) Medium Specimen Retrieval Bag, REF 5500-000-003, Rx Only Product Usage: The device is a single-use specimen retrieval bag indicated for use in laparoscopic procedures to capture and remove organs or tissue from the body cavity.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2299-2015·2015-05-27

    Greystone Foods Recalls Broccoli Florets Due to Possible Listeria Contamination

    Greystone Foods is recalling 1,692 bags of Today's Harvest Broccoli Florets due to possible Listeria monocytogenes contamination. The product was distributed in Florida and Georgia.

    Product
    Today's Harvest(TM) Broccoli Florets, GRADE A SELECT, NET WT. 2 LBS., (907 g), KEEP FROZEN, packed by Greystone Foods, LLC, Birmingham, Alabama 35209
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-1622-2015·2015-05-27

    Roche Homocysteine Test System Recalled for Inaccurate Low Results

    Roche Diagnostics is recalling Homocysteine Reagent lots due to complaints of under-recovery and falsely low patient results, which could delay diagnosis of peripheral vascular disease.

    Product
    Homocysteine test system - Homocysteine Reagent. 05385415190; Homocysteine 100 Tests, cobas c, COBAS INTEGRA Homocysteine Enzymatic Assay is an in vitro test for the quantitative determination of total L-homocysteine in human serum and plasma on Roche/Hitachi cobas c…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1629-2015·2015-05-27

    Siemens IMMULITE TBG Test Kits Recalled for Inaccurate Results

    Siemens Healthcare Diagnostics is recalling 155 IMMULITE TBG test kits because they may produce falsely low thyroid test results.

    Product
    IMMULITE/IMMULITE 1000 Systems TBG, catalog LKTB1 Quantitative measurement of Thyroxine-Binding Globulin (TBG) in serum, as an aid in the diagnosis and treatment of thyroid diseases.
    Category
    Medical Device
    Distribution
    0 states