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.

38551–38575 of 50506

  • HighFDA (Devices)·Z-1702-2015·2015-06-10

    Alcon Custom Pak Recalled for Potential Glove Splits and Holes

    Alcon Research, Ltd. is recalling Alcon Custom Paks because the Devon Light Glove component may have splits or holes, which could lead to surgical site infections.

    Product
    The Alcon Custom Pak. The Alcon Customer Pak is an assemblage of single-use medical devices and accessories designed by medical professionals for specific ophthalmic surgical procedures. Some Paks contain the Devon Light Glove.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15C002000·2015-06-10

    Baby Jogger Recalls Infant Car Seats Due to Labeling Errors

    Baby Jogger is recalling specific infant car seats because labels and manuals contain incorrect or missing safety information, which may increase injury risk in a crash.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·089-2015·2015-06-09

    Big Easy Foods Recalls Stuffed Chicken for Undeclared Wheat Allergen

    Big Easy Foods is recalling approximately 93,006 pounds of raw and cooked stuffed chicken products because they contain wheat, an undeclared allergen.

    Product
    Big Easy Foods of Louisiana, LLC — Big Easy Foods Louisiana Cuisine, Inc. Recalls Poultry Product Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    10 states
  • HighNHTSA·15V356000·2015-06-09

    Gulf Stream Recalls 2015 Trailers Due to Failing Entry Step Rivets

    Gulf Stream is recalling 2015 Canyon Trail and Sedona trailers because entry step rivets may shear, causing steps to fail and increasing the risk of falls.

    Product
    GULF STREAM — GULF STREAM CANYON TRAIL, SEDONA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V355000·2015-06-09

    Vermeer Recalls 2015 TLR30HD and TLR30LD Trailers for Safety Chain Defect

    Vermeer is recalling specific 2015 TLR30HD and TLR30LD trailers because an incorrectly installed safety chain may fail to prevent the trailer from separating from the tow vehicle.

    Product
    VERMEER — VERMEER TLR30HD, TLR30LD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·088-2015·2015-06-06

    Benedetti Farms Recalls Chicken and Turkey Sausage for Misbranding

    Benedetti Farms is recalling approximately 11,670 pounds of chicken and turkey sausage products because hog and sheep casings were not listed on the labels.

    Product
    Benedetti Farms — Benedetti Farms, Inc. Recalls Chicken and Turkey Sausage Products Due To Misbranding
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·15V350000·2015-06-05

    Nova Bus Recalls 2001-2004 LFS Buses for Parking Brake Hose Defect

    Nova Bus is recalling 250 model year 2001-2004 LFS buses because incorrectly connected air hoses may delay parking brake application, increasing crash risk.

    Product
    NOVA BUS — NOVA BUS NOVA LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V348000·2015-06-05

    Prevost Recalls Coaches Due to Fire Suppression Wiring Damage Risk

    Prevost is recalling 452 model year 2010-2014 coaches because engine heat may damage fire suppression wires, potentially causing an engine shutdown and crash.

    Product
    PREVOST — PREVOST H3-45, X3-45, H3-41, XLII-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15159·2015-06-04

    Cree Recalls LED T8 Lamps Due to Overheating and Burn Hazard

    Cree Inc. is recalling approximately 700,000 LED T8 replacement lamps sold in the U.S. because electrical arcing can cause the lamps to overheat and melt, posing a burn hazard.

    Product
    Cree® LED T8 replacement lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15158·2015-06-04

    Big Lots Recalls Hanging Chairs Due to Fall Hazard

    Big Lots is recalling about 16,000 hanging chairs because they can tip over and cause falls. Consumers should stop using them and return the base for a refund.

    Product
    Hanging chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·086-2015·2015-06-04

    Demes Gourmet Recalls Chicken Longanisa Due to Unlabeled Hog Casings

    Demes Gourmet Corp. is recalling approximately 29,052 pounds of chicken longanisa because the products were wrapped in hog casings not listed on the labels.

    Product
    Demes Gourmet Corporation — Demes Gourmet Corp. Recalls Chicken and Pork Products Due To Misbranding
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-1691-2015·2015-06-03

    Biosense Webster Recalls SMARTABLATE RF Generator Systems Due to Unintended Energy Delivery

    Biosense Webster is recalling 115 SMARTABLATE RF Generator Systems because two complaints reported the device inadvertently delivered RF energy during procedures.

    Product
    SMARTABLATE RF Generator System, Catalog No. M490006, M490007, M4900106, and M4900107. Product Usage: The use of the SMART ABLATE Generator and all accessories is indicated in combination with compatible therapeutic catheters for use in conventional intracardiac RF ablation…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1655-2015·2015-06-03

    Philips Brilliance CT 6 Air Systems Recalled for Unexpected Couch Descent

    Philips is recalling 153 Brilliance CT 6 Air systems because the patient couch unexpectedly descended during exams. The units were distributed in China.

    Product
    Brilliance CT 6 Air. 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 (Devices)·Z-1652-2015·2015-06-03

    Philips Brilliance CT 16 Water Computed Tomography Systems Recalled for Couch Descent

    Philips Medical Systems is recalling 153 Brilliance CT 16 Water systems because the patient couch may unexpectedly descend during an exam.

    Product
    Brilliance CT 16 Water. 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-2335-2015·2015-06-03

    Metro Market Lemon Pepper Rub Recalled for Undeclared Wheat Allergen

    The Regency Group, Inc. is recalling Metro Market Lemon Pepper Rub due to contamination with gluten (wheat) that is not declared on the label.

    Product
    Metro Market Lemon Pepper Rub, stock code 11525, packaged in 25 lbs. container. No UPC.
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1688-2015·2015-06-03

    Terumo Advanced Perfusion System 1 Base Recalled for Power Loss

    Terumo is recalling 1,713 Advanced Perfusion System 1 bases worldwide to address power loss issues. The recall involves design changes and switch protectors.

    Product
    Base for Terumo Advanced Perfusion System 1, 220/240V 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-1678-2015·2015-06-03

    Halyard KimVent Closed Suction System Recalled for Potential Valve Defect

    Halyard Health is recalling specific KimVent Turbo-Cleaning Closed Suction Systems for adults because a defective internal valve may allow air to leak from the ventilator circuit.

    Product
    KimVent Turbo-Cleaning Closed Suction System for Adults, 10 F T-Piece (Product Code 227105); KimVent Turbo-Cleaning Closed Suction System for Adults, 12 F, DSE (Product Code 2271603); KimVent Turbo-Cleaning Closed Suction System for Adults, 12 F, T-Piece (Product Code 227135).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1684-2015·2015-06-03

    Codman 3000 Series Refill Set Recalled for Leaking Needles

    Codman & Shurtleff, Inc. is recalling 5,463 units of the CODMAN 3000 Series Refill Set because the needles may leak from the hub connection.

    Product
    CODMAN 3000 Series Refill Set- Huber needles. Used in combination with the CODMAN 3000 Series Constant Flow Implantable Pump CATALOG NO. : AP-07014 Each CODMAN 3000 Refill Kit contains 2 (two) 22 Gauge x 1.5 Huber Point Needles which are used in conjunction with a 50 mL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V342000·2015-06-03

    Volvo Recalls 2016 XC90 Vehicles for Side Air Bag Wiring Defect

    Volvo is recalling 2016 XC90 vehicles because incorrect side air bag wiring may disable the safety feature, increasing injury risk in a crash.

    Product
    VOLVO — VOLVO XC90
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1681-2015·2015-06-03

    Medtronic Recalls SynchroMed II Implantable Pumps Due to Alarm Failure

    Medtronic is recalling specific SynchroMed II implantable drug pumps because the audible alarm may stop working, potentially preventing patients from detecting issues.

    Product
    Medtronic SynchroMed II Implantable Infusion Pumps, models 8637-20 and 8637-40. Sterile. Product Usage: The implantable Medtronic SynchroMed II programmable pumps are part of an infusion system that stores and delivers a prescribed drug to a specific site. The implanted…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2336-2015·2015-06-03

    Regency Group Recalls Pizza Seasoning for Undeclared Wheat Allergen

    Regency Group is recalling specific lots of pizza seasoning because the product contains gluten (wheat) but the label does not declare it.

    Product
    Pizza Seasoning, stock code 03388, packaged in 20 lbs. or 50 lbs. container. The UPC is 0 23605 03388 4.
    Category
    Food
    Distribution
    8 states
  • HighFDA (Devices)·Z-1677-2015·2015-06-03

    Alere i Influenza A & B kits recalled for false negative risk

    Alere Scarborough, Inc. is recalling specific lots of Alere i Influenza A & B kits due to a high invalid rate and increased risk of false negative results.

    Product
    Alere i Influenza A & B Product Usage: The Alere i Influenza A and B assay, performed on the Alere i Instrument, is a rapid molecular in vitro diagnostic test utilizing an isothermal nucleic acid amplification technology for the qualitative detection and discrimination of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1649-2015·2015-06-03

    Philips Brilliance CT 64 Systems Recalled for Unexpected Couch Descent

    Philips is recalling 153 Brilliance CT 64 systems because the patient couch may unexpectedly descend during an exam.

    Product
    Brilliance CT 64. 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