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.

22101–22125 of 50429

  • HighFDA (Food)·F-1536-2020·2020-09-30

    Freshouse and Nature Promise Limes Recalled for Listeria Risk

    Freshouse Produce is recalling Freshouse and Nature Promise limes after environmental sampling tested positive for Listeria monocytogenes.

    Product
    Freshouse Limes, 2lb mesh bag, UPC 33383 14683 & Nature Promise Organic Limes, 1lb mesh bag, UPC 88267 53813
    Category
    Food
    Distribution
    5 states
  • HighFDA (Devices)·Z-2990-2020·2020-09-30

    Hologic Recalls Panther Fusion Tube Trays Due to Potential Leaks

    Hologic is recalling 607 Panther Fusion Tube Trays because they may leak, potentially invalidating patient results or causing false negatives in flu and RSV assays.

    Product
    Panther Fusion Tube Tray, Part: FAB-15004, REF: PRD-04000
    Category
    Medical Device
    Distribution
    25 states
  • HighFDA (Food)·F-1543-2020·2020-09-30

    Gilster-Mary Lee Recalls Buttered Microwave Popcorn Due to Glass Fragments

    Gilster-Mary Lee Corp. is recalling specific brands of buttered microwave popcorn because tempered glass fragments were found in the product.

    Product
    Buttered microwave popcorn packaged in the following ways: 1) Full Circle Organic Microwave Popcorn Butter, 3-3.3 oz (94 g) bags, Net Wt. 9.9 oz (281 g), Distributed by Topco Associates LLC, Elk Grove Villiage, IL, UPC 36800-40609 2) Sprouts Farmers Market, Organic Butter…
    Category
    Food
    Distribution
    21 states
  • HighNHTSA·20V600000·2020-09-30

    2021 Entegra motorhomes recalled for power seat wiring fire risk

    Jayco is recalling 2021 Entegra motorhomes with Villa power seats because the electrical wiring may become damaged or chafed, causing short circuits and fire risk.

    Product
    ENTEGRA — ENTEGRA REATTA XL, ASPIRE, CORNERSTONE, ANTHEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2988-2020·2020-09-30

    LivaNova Recalls Perceval Dual Collapser Due to Valve Collapse Failure

    LivaNova is recalling specific lots of the Perceval Dual Collapser because complaints indicate the device may fail to collapse the heart valve during implantation.

    Product
    Perceval Dual Collapser, Size S/M, REF: ICV1235, Sterile EO, Rx Only, CE, UDI: 08022057014832 - Product Usage: he Dual Collapser is a component of the Perceval single use accessory kits used to reduce the Perceval Sutureless heart valve diameter before valve implant, allowing…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2987-2020·2020-09-30

    LivaNova Recalls Perceval Single Use Accessory Kits Due to Collapse Failure

    LivaNova is recalling specific lots of Perceval Single Use Accessory Kits because the Dual Collapser component may fail to reduce the heart valve diameter during implantation.

    Product
    Perceval Single Use Accessory Kit, Size M, REF: ICV1350, Sterile EO, Rx Only, CE, UDI: 8022057015259 - Product Usage: he Dual Collapser is a component of the Perceval single use accessory kits used to reduce the Perceval Sutureless heart valve diameter before valve implant…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2995-2020·2020-09-30

    GE Healthcare Recalls NM 830 Medical Detectors Due to Loose Screws

    GE Healthcare is recalling 25 NM 830 detectors because rotor bearing screws were found loose. The devices are distributed in the US and internationally.

    Product
    NM 830 Model # H3910AC
    Category
    Medical Device
    Distribution
    27 states
  • HighFDA (Food)·F-1545-2020·2020-09-30

    Cadia Organic Unsalted Microwave Popcorn Recalled for Foreign Matter

    Gilster-Mary Lee Corp. is recalling Cadia Organic Unsalted Microwave Popcorn due to the presence of tempered glass fragments.

    Product
    Cadia Organic Unsalted Microwave Popcorn, Net Wt. 8.4 oz (238 g) 3-2.8 oz (79 g) bags, KeHDistributors LLC, Naperville, IL, UPC 15369-01289
    Category
    Food
    Distribution
    21 states
  • HighFDA (Devices)·Z-2999-2020·2020-09-30

    ArthroCare Speed Stitch Needle Cassettes Recalled for Potential Breakage

    ArthroCare is recalling Speed Stitch Needle Cassettes because a supplier error may have resulted in needles made of titanium instead of stainless steel, posing a risk of breakage during use.

    Product
    Speed Stitch Needle Cassette
    Category
    Medical Device
    Distribution
    42 states
  • HighNHTSA·20V594000·2020-09-29

    2021 Newmar Motorhomes Recalled for Leveling Jack Fastening Defect

    Newmar is recalling certain 2021 motorhome models because the front leveling jacks may not be properly fastened to the chassis. If the jacks fail, the motorhome could unexpectedly drop, creating an injury risk.

    Product
    NEWMAR — NEWMAR ESSEX, DUTCH STAR, MOUNTAIN AIRE, LONDON AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E072000·2020-09-29

    Spartan Fire Recalls Gladiator and MetroStar Vehicles Due to Gauge Defect

    Spartan Fire is recalling 2018-2019 Gladiator and MetroStar vehicles because replacement gauges may prevent the Advanced Protection System from engaging, increasing injury risk in crashes.

    Product
    SPARTAN — SPARTAN, SPARTAN FIRE METROSTAR, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V591000·2020-09-25

    2020-2021 Dynamax Isata Motorhomes Recalled for Engine Software Fire Risk

    Forest River is recalling 2020-2021 Dynamax Isata motorhomes due to engine software that fails to provide adequate warmup protection. The defect can cause bearing damage and engine block failure, risking oil leaks and fires.

    Product
    DYNAMAX — DYNAMAX ISATA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V589000·2020-09-25

    2021 Forest River Wildwood RV Cooktop May Pose Fire Risk

    Forest River is recalling 2021 Wildwood and Salem trailers. The cooktop flame may invert due to furnace air leakage, increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V588000·2020-09-24

    2020 Cadillac CT5 Electronic Brake Boost System Defect

    General Motors is recalling the 2020 Cadillac CT5 due to sensor contamination in the electronic brake boost system, which may reduce braking effectiveness and increase crash risk. GM will replace the module at no cost.

    Product
    CADILLAC — CADILLAC, CHEVROLET, BUICK XT4, CT4, CORVETTE, CT5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20782·2020-09-24

    Vthrive Bioactive Multivitamins Recalled for Non-Child-Resistant Packaging

    The Vitamin Shoppe is recalling Vthrive Bioactive Women's One-Daily Multi vitamins because the packaging is not child-resistant, posing a poisoning risk to young children.

    Product
    Vthrive Bioactive Women's One-Daily Multi vitamins
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V585000·2020-09-24

    2020-2021 Land Rover Range Rover Sport TPMS Software Malfunction Recall

    2020-2021 Land Rover Range Rover Sport vehicles have incorrect TPMS pressure settings that prevent the warning light from activating when tire pressure drops dangerously low. Owners should contact Land Rover to schedule a free software update.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20190·2020-09-23

    Specialized Recalls Sirrus Bicycles with Alloy Cranks Due to Fall Hazards

    Specialized Bicycle Components is recalling approximately 36,000 Sirrus, Sirrus X, and Sirrus Sport bicycles in the U.S. because the alloy crank arms can disengage, posing fall and injury hazards.

    Product
    Sirrus, Sirrus X and Sirrus Sport Bicycles with alloy cranks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2964-2020·2020-09-23

    Cook Zenith Alpha Abdominal Endovascular Graft Recalled for Excess Glue

    Cook Inc. is recalling Zenith Alpha Abdominal Endovascular Grafts due to excess glue in the delivery system handle, which may prevent full deployment.

    Product
    Zenith Alpha Abdominal Endovascular Graft - Distributed OUS only. Indicated for the endovascular treatment of patients with abdominal aortic or aorto-iliac aneurysms Reference Part Number (RPN): ZIMB-22-108 ZIMB-22-118 ZIMB-22-128 ZIMB-22-70 ZIMB-22-84 ZIMB-22-98…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2970-2020·2020-09-23

    Siemens epoc BGEM Test Card Recalled for Inconsistent Glucose Results

    Siemens Healthcare Diagnostics Inc is recalling specific lots of epoc BGEM Test Cards due to sporadically inconsistent low glucose results that could delay diagnosis or cause unnecessary treatment.

    Product
    Siemens epoc BGEM Test Card-In vitro diagnostic device for the quantitative testing of samples of heparinized or un-anticoagulated arterial, venous or capillary whole blood in the laboratory or at the point of care SMN#/Model #: 10736382
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20192·2020-09-23

    Kobalt Cordless Electric Pole Saws Recalled for Laceration Hazard

    Kobalt 40-volt cordless electric pole saws are being recalled because the switch can fail, causing the saw to continue running and posing a laceration risk.

    Product
    Kobalt brand 40-volt Lithium Ion 8-inch Cordless Electric Pole Saws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1523-2020·2020-09-23

    Blue Apron Recalls Spicy Beef Meal Kits Due to Salmonella Risk

    Blue Apron is recalling Spicy Beef & Vegetables meal kits delivered the week of July 27, 2020, because the onions may be contaminated with Salmonella.

    Product
    Spicy Beef & Vegetables with Rice & Sesame Seeds meal kits containing onions delivered the week of July 27, 2020.
    Category
    Food
    Distribution
    37 states