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.

33651–33675 of 50502

  • HighFDA (Food)·F-0732-2017·2016-12-21

    Publix Danish Apple Coffee Cake Recalled for Metal Shavings

    Publix Super Markets is recalling Danish Apple Coffee Cake strips due to the presence of small metal shavings. The product was distributed in six southeastern states.

    Product
    Publix Danish Apple Coffee Cake Strip, 15 oz. UPC 002-19562-00000
    Category
    Food
    Distribution
    6 states
  • HighFDA (Devices)·Z-0766-2017·2016-12-21

    Encore Medical Recalls Empowr PS Knee System Box Cut Guides

    Encore Medical is recalling 162 Empowr PS Knee System Box Cut Guides because femoral chipping occurred during surgery.

    Product
    Empowr PS Knee System Box Cut Guide The EMPOWER PS Box Cut Guide is used to make the housing resection for the post of the posterior stabilized implant
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0731-2017·2016-12-21

    Elekta Recalls MOSAIQ Oncology Information System Due to Data Saving Error

    Elekta is recalling 47 MOSAIQ Oncology Information System units because edits to particle field definition parameters may not be saved.

    Product
    MOSAIQ Oncology Information System The product is used to manage workflows for treatment planning and delivery. It supports information flow among healthcare facility personnel and can be use wherever radiotherapy and chemotherapy are prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0681-2017·2016-12-21

    Giant Eagle Recalls Buffalo Hot Peanuts Due to Undeclared Cashews and Wheat

    Giant Eagle is recalling 248 units of Farmers Market Buffalo Hot Peanuts because they contain undeclared cashews and wheat. The error was caused by mislabeling at the manufacturer.

    Product
    Clear plastic cup labeled as: The Farmers Market Buffalo Hot Peanuts; Net Wt. 5 oz.; UPC 3003499846; Best By 10/25/2016
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-0767-2017·2016-12-21

    Firefly Medical Recalls IVEA 500A Medical Beds Due to Dowel Pin Defect

    Firefly Medical is recalling 239 IVEA 500A medical beds because a dowel pin could slip out, causing the bed to slump and potentially making a patient stumble.

    Product
    IVEA 500A Intended for Med-Surg patient care.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0733-2017·2016-12-21

    Cook Medical Recalls Central Venous Catheter Trays Due to Incorrect Needles

    Cook Medical is recalling 99 units of Spectrum Minocycline/Rifampin Impregnated Central Venous Catheter Trays because they may contain incorrect needles, potentially preventing wire guide passage.

    Product
    Cook Spectrum Minocycline/Rifampin Impregnated Double Lumen Central Venous Catheter Tray Cook Spectrum Minocycline/Rifampin Impregnated Triple Lumen Central Venous Catheter Tray
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0729-2017·2016-12-21

    Merge Cardio software recalled for potential report matching errors

    Merge Healthcare is recalling Merge Cardio software versions 8.30.0 through 10.1.1 because images sent without an order may be matched to the wrong accession number.

    Product
    Merge Cardio software. Merge Cardio is a system intended to be used to acquire, store, print, transfer, and archive clinical information including images, Hemodynamic studies and reports, measurements (via import from DICOM Structured Reporting, text files or optical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0743-2017·2016-12-21

    Cargill Recalls Crisco Professional Liquid Butter Alternative for Excessive Additives

    Cargill is recalling Crisco Professional Liquid Butter Alternative because it contains excessive amounts of TBHQ and DMPS. The product was distributed to 29 states.

    Product
    Crisco PROFESSIONAL Liquid Butter Alternative, SALTED FOR ADDED FLAVOR, NET/NETO 1 GAL (3.79 L) INGREDIENTS; Corn Oil, Soybean Oil, Sunflower Oil, Hydrogenated Soybean Oil, Salt, Soy Lecithin***TBHQ ***Dimethylpolysiloxane***CONTAINS: SOY. UPC 7 81525 64775 7
    Category
    Food
    Distribution
    29 states
  • HighFDA (Devices)·Z-0755-2017·2016-12-21

    GE Healthcare Recalls Avance and Amingo Anesthesia Devices Due to Malfunction Risk

    GE Healthcare is recalling specific Avance CS2, Avance, and Amingo anesthesia devices because they may enter a System Malfunction state if a storage drawer closes with excessive force.

    Product
    GE Healthcare, Avance, Avance CS2, Amingo.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0732-2017·2016-12-21

    GF Health Products Recalls Patriot Homecare Beds Due to Motor Defect

    GF Health Products is voluntarily correcting Patriot homecare beds because contaminated motor housings may crack, potentially causing the head section to fall.

    Product
    Lumex, Patriot Full Electric Homecare Bed, & Patriot LX Full Electric Homecare Bed containing the Okin Dumat 3 Head/Foot Motors. Description Part Number Motor and Pendant Patriot Full Electric 120V…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0734-2017·2016-12-21

    Accuray Recalls CyberKnife Systems Due to Unexpected Robot Motion

    Accuray is recalling 40 CyberKnife Robotic Radiosurgery Systems with software version 10.6 due to a potential safety issue involving unexpected treatment robot motion when removing an accessory.

    Product
    CyberKnife Robotic Radiosurgery System using software version 10.6; Catalog/Part Number: 54000 UDI: M658053301 0 Radiology: The CyberKnife Robotic Radiosurgery System is indicated for treatment planning and image guided stereotactic Radiosurgery and precision radiotherapy…
    Category
    Medical Device
    Distribution
    12 states
  • HighNHTSA·16V912000·2016-12-20

    C&M Recalls 2016 Trailers with Missing Front Reflex Reflectors

    C&M Trailers is recalling 670 model year 2016 boat, jet ski, and utility trailers because they may be missing front reflex reflectors, which could make them harder to see.

    Product
    C&M — C&M BOAT TRAILER, JET SKI TRAILER, UTILITY TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V914000·2016-12-20

    BMW, MINI, and Rolls-Royce Recall for Air Bag Initiator Defect

    BMW is recalling 2016-2017 vehicles because seat-mounted air bag initiators may fail to ignite, preventing deployment and increasing injury risk.

    Product
    BMW — BMW, MINI, ROLLS-ROYCE X1 SAV, 550I, M5, 535D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V911000·2016-12-19

    Nissan Recalls Altima, Rogue, and Maxima for Air Bag Sensor Defect

    Nissan is recalling specific 2013-2016 Altima, Rogue, and Maxima vehicles because an incorrect air bag sensor may misclassify front passengers, increasing injury risk in crashes.

    Product
    NISSAN — NISSAN ALTIMA, ROGUE, MAXIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V906000·2016-12-16

    Toyota Recalls 2016 Avalon and 2017 Camry for Knee Air Bag Fastener Issue

    Toyota is recalling specific 2016 Avalon and 2017 Camry vehicles because the front passenger knee air bag may be attached with incorrect fasteners, which could affect deployment and increase injury risk.

    Product
    TOYOTA — TOYOTA AVALON, CAMRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V910000·2016-12-16

    RAM ProMaster Recall: Side Air Bag Inflator May Fail to Ignite

    Chrysler is recalling 2017 RAM ProMaster vehicles because the seat-mounted side air bag inflator initiator may fail to ignite during a crash.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V909000·2016-12-16

    C&M Utility Trailer Recall for Missing Tire Placard Information

    C&M is recalling 2015-2016 Utility trailers because the tire placard may lack required size information, which could lead to incorrect tire replacements.

    Product
    C&M — C&M UTILITY TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V907000·2016-12-16

    Chrysler Recalls 2016 Jeep and Dodge Vehicles for Engine Stalling Risk

    Chrysler is recalling 42,231 model year 2016 Jeep Compass, Jeep Patriot, and Dodge Journey vehicles because an intermittent sensor may cause the engine to stall, increasing crash risk.

    Product
    JEEP — JEEP, DODGE PATRIOT, COMPASS, JOURNEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V908000·2016-12-16

    Keystone Recalls Fifth Wheel Trailers Due to Rear Door Hinge Welds

    Keystone is recalling 2016-2017 fifth wheel trailers because rear cargo door hinge welds may be insufficient, causing the door to swing down with excessive force.

    Product
    KEYSTONE — KEYSTONE, DUTCHMEN RAPTOR, FUZION, VOLTAGE, CARBON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17720·2016-12-15

    Figi's Recalls Christmas Wishes Tins Due to Choking and Battery Hazards

    Figi's Companies is recalling Christmas Wishes tins because the sound chip mechanism can separate, exposing button batteries that pose choking and ingestion hazards to children.

    Product
    Christmas Wishes tins
    Category
    Consumer Product
    Distribution
    Distributed nationwide