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.

28626–28650 of 50488

  • HighFDA (Devices)·Z-2103-2018·2018-06-13

    NordicNeuroLab fMRI AudioSystem Recalled for Acoustic Distortion and Heat

    NordicNeuroLab AS is recalling 64 fMRI AudioSystem units after a patient reported acoustic distortion and heat from headphones during a scan.

    Product
    fMRI Hardware System - AudioSystem, Version 1.0 The AudioSystem allows auditory signals from the stimulus presentation PC to enter the scanner room and to be presented to the patient. A communication console allows the operator to adjust the sounds from the PC and to speak to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2084-2018·2018-06-13

    Tosoh ST-AIA PACK HCG Assay Recalled Due to Strensiq Interference

    Tosoh Bioscience Inc is recalling ST-AIA PACK HCG assays because Asfotase Alfa (Strensiq) interferes with the test, potentially causing inaccurate results.

    Product
    ST-AIA PACK HCG; Part Number: 025256 Assay, Reproductive Hormone
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1614-2018·2018-06-13

    11-VI Incorporated Recalls Non-Certified Laser Diode Components for Firearms

    11-VI Incorporated is recalling 323,972 non-certified laser diode components used in firearm sights because they emit more than the 5 mW limit.

    Product
    11-VI Incorporated Laser diode component Non-certified laser diode component used in laser sights for firearms
    Category
    Consumer Product
    Distribution
    1 state
  • HighFDA (Devices)·Z-2082-2018·2018-06-13

    Tosoh Thyroid Assay Recalled Due to Strensiq Interference

    Tosoh Bioscience Inc is recalling ST-AIA PACK TU thyroid assays because the drug Strensiq can cause inaccurate test results.

    Product
    ST-AIA PACK TU; Part Number: 025270 Assay, Thyroid
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2070-2018·2018-06-13

    Tosoh Tumor Marker Assay Recalled Due to Strensiq Interference

    Tosoh Bioscience Inc. is recalling ST-AIA PACK 27.29 tumor marker assays because Asfotase Alfa (Strensiq) interferes with the tests, potentially causing inaccurate results.

    Product
    ST-AIA PACK 27.29; Part Number: 025202 Assay, Tumor Marker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2098-2018·2018-06-13

    Tosoh Tumor Marker Assay Recalled Due to Strensiq Interference

    Tosoh Bioscience Inc is recalling ST-AIA PACK BMG tumor marker assays because Asfotase Alfa (Strensiq) interferes with the tests, potentially causing inaccurate results.

    Product
    ST-AIA PACK BMG; Part Number:025259 Assay, Tumor Marker
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1539-2018·2018-06-13

    Trader Joe's Organic French Baguette Recalled for Listeria Risk

    Trader Joe's is recalling specific lots of Organic French Baguettes due to potential Listeria monocytogenes contamination.

    Product
    Trader Joe's Artisan Bread - Organic French Baguette; (Brown and Serve) Keep frozen; Product code 53835; 24 x 11.5 oz. (326g) - 24 loaves per case. UPC 0053 8350 Product of Canada Manufactured by Groupe Premiere Moisson Inc., 189 Harwood, Vaudreuil-Dorion, Quebec…
    Category
    Food
    Distribution
    12 states
  • HighFDA (Devices)·Z-2129-2018·2018-06-13

    Orthofix Recalls Lapidus Plates Due to Screw Engagement Failure

    Orthofix is voluntarily recalling 156 Lapidus Plates because locking screws failed to properly engage the plates during surgery.

    Product
    Lapidus Plate, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label, Size/Step/Left or Right (Part Number): a) Small/0MM Step/Left (002-C-01000L); b) Small/0MM Step/Right (002-C-01000R); c) Large/0MM Step/Left (002-C-02000L); d) Large/0MM Step/Right (002-C-02000R); e)…
    Category
    Medical Device
    Distribution
    19 states
  • HighFDA (Devices)·Z-2119-2018·2018-06-13

    Orthofix Non-Locking Screws Recalled Due to Failure to Engage Plates

    Orthofix, Inc. is voluntarily recalling specific non-locking screws from the Rival Reduce Fracture Plating System and Rival View Plating System because they failed to properly engage plates during surgery.

    Product
    Non-Locking Screw, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label. Size (Part Number): a) D 2.0MM X 8MM (0002-D-20008); b) D 2.0MM X 10MM (002-D-20010); c) D 2.0MM X 12MM (002-D-20012); d) D 2.0MM X 14MM (002-D-20014); e) D 2.0MM X 16MM (002-D-20016); f) D 2.0MM X 18MM…
    Category
    Medical Device
    Distribution
    19 states
  • HighCPSC·18747·2018-06-12

    Ashley Furniture Recalls Amnon Floor Lamps Due to Burn Hazard

    Ashley Furniture is recalling Amnon floor lamps because the incorrect wattage label allows users to install bulbs that can melt the power switch, posing a burn hazard.

    Product
    Amnon floor lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18174·2018-06-12

    A&I Recalls Tractor Canopies Due To ROPS Failure Injury Hazard

    A&I is recalling about 6,200 tractor canopies in the U.S. and 265 in Canada because they may fail to protect operators in a rollover accident.

    Product
    A&I tractor canopies
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18176·2018-06-12

    Uttermost Recalls Mirrors and Wall Decor Due to Falling Hazard

    Uttermost is recalling about 17,000 mirrors and wall decor items because the hanging hardware can break, causing items to fall and injure bystanders.

    Product
    Mirrors, art and wall decor
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·048-2018·2018-06-12

    J Bar B Foods Recalls Beef Sausage for Undeclared Pork Casing

    J Bar B Foods is recalling beef brisket smoked sausage products because they contain an undeclared pork casing, which may cause allergic reactions.

    Product
    J Bar B Foods — J Bar B Foods Recalls Beef Sausage Products due to Adulterated and Misbranded Ingredient
    Category
    Food
    Distribution
    1 state
  • HighCPSC·18177·2018-06-12

    Lorex Recalls Three Video Monitor Models Due to Battery Burn Hazard

    Lorex is recalling three video monitor models because the batteries can overheat and swell, posing a burn hazard. Consumers should stop using the monitors and contact Lorex for a refund.

    Product
    Lorex video monitors models LW2751, LW2752 and LW2962H
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V393000·2018-06-12

    KME Predator Aerial Vehicles Recalled for Tether Control Software Defect

    Kovatch Mobile Equipment is recalling 2015-2018 KME Predator Aerial emergency vehicles because the aerial platform may continue moving if the tether control is unplugged.

    Product
    KME — KME PREDATOR AERIAL, PREDATOR SS AERIAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18175·2018-06-12

    Ketra Recalls D3 Recessed Downlights Due to Electrical Shock Hazard

    Ketra is recalling about 3,400 D3 recessed downlights because incorrect wiring in the power supply connectors poses an electrical shock hazard. No injuries have been reported.

    Product
    Ketra D3 recessed downlights
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V387000·2018-06-08

    Newmar Recalls 2018-2019 Motorhomes Due to Windshield Wiper Defect

    Newmar is recalling 2018-2019 Essex, London Aire, King Aire, and Mountain Aire motorhomes because windshield wiper arms may not contact the glass, reducing visibility.

    Product
    NEWMAR — NEWMAR ESSEX, LONDON AIRE, KING AIRE, MOUNTAIN AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V379000·2018-06-07

    Altec Recalls 2016-2017 Aerial Devices and Digger Derricks for Grounding Defect

    Altec is recalling 2016-2017 Aerial Devices and Digger Derricks because improperly sized cable connection receptacles may cause the high voltage grounding system to fail, increasing the risk of injury.

    Product
    ALTEC — ALTEC DIGGER DERRICK, AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V382000·2018-06-07

    Mobility Ventures Recalls MV-1 Vehicles for Turn Signal Defect

    Mobility Ventures is recalling 2015-2016 MV-1 vehicles because a failed rear turn signal does not alert the driver, increasing crash risk.

    Product
    MOBILITY VENTURES — MOBILITY VENTURES MV-1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V376000·2018-06-07

    Forest River Recalls 2017-2018 Glaval Transit Buses for Seat Belt Defect

    Forest River is recalling 2017-2018 Glaval transit buses because a washer in the driver's seat belt assembly may break, allowing the belt to separate from the vehicle.

    Product
    GLAVAL BUS — GLAVAL BUS TITAN II LOW FLOOR, ENTOURAGE, CONCORDE II, COMMUTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V380000·2018-06-07

    Volkswagen Recalls 2018 Atlas Models for Seat Belt Buckle Damage Risk

    Volkswagen is recalling 54,729 2018 Atlas vehicles because missing manual information can lead to seat belt buckle damage, increasing injury risk in crashes.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2000-2018·2018-06-06

    Arrow International Recalls Central Venous Catheter Kits Due to Sterility Concerns

    Arrow International Inc is recalling 416,055 ARROWg+ard Blue PLUS Multi-Lumen Central Venous Catheterization Kits because unsealed packaging may compromise product sterility.

    Product
    ARROWg+ard Blue PLUS(R) Multi-Lumen Central Venous Catheterization Kit; Product Code: ASK-42703-SJH
    Category
    Medical Device
    Distribution
    Distributed nationwide