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.

24451–24475 of 50442

  • HighFDA (Devices)·Z-0479-2020·2019-11-27

    Cook Inc. Recalls Torcon NB Advantage Catheters Due to Sterility Concerns

    Cook Inc. is recalling 30 Torcon NB Advantage Catheters because undersealed packaging pouches may compromise sterility. The devices are distributed worldwide.

    Product
    Torcon NB Advantage Catheters - Product Usage: Intended for use in the peripheral and coronary vascular system, including the carotid arteries, in giographic procedures by physicians trained and experienced in angiographic techniques.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0460-2020·2019-11-27

    Cook Inc. Recalls Torcon NB Advantage Catheters Due to Packaging Seal Defect

    Cook Inc. is recalling Torcon NB Advantage Catheters because undersealed packaging pouches may compromise sterility. The recall covers units distributed in the US and internationally.

    Product
    Torcon NB Advantage Catheters - Product Usage: Intended for use in the peripheral and coronary vascular system, including the carotid arteries, in giographic procedures by physicians trained and experienced in angiographic techniques.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0468-2020·2019-11-27

    Cook Inc. Recalls Torcon NB Advantage Catheters Due to Sterility Concerns

    Cook Inc. is recalling 232 Torcon NB Advantage Catheters because undersealed packaging pouches may compromise sterility. The devices are distributed worldwide.

    Product
    Torcon NB Advantage Catheters - Product Usage: Intended for use in the peripheral and coronary vascular system, including the carotid arteries, in giographic procedures by physicians trained and experienced in angiographic techniques.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0478-2020·2019-11-27

    Cook Inc. Recalls Torcon NB Advantage Catheters Due to Sterility Concerns

    Cook Inc. is recalling 195 Torcon NB Advantage Catheters because undersealed packaging pouches may have compromised the sterility of the devices.

    Product
    Torcon NB Advantage Catheters - Product Usage: Intended for use in the peripheral and coronary vascular system, including the carotid arteries, in giographic procedures by physicians trained and experienced in angiographic techniques.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·20710·2019-11-26

    Yamaha Recalls Portable Generators Due to Fire and Burn Hazards

    Yamaha is recalling 2018 and 2019 EF2000iS portable generators because the fuel tank can leak gasoline, posing fire and burn hazards.

    Product
    2018 and 2019 Yamaha EF2000iS portable generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V841000·2019-11-21

    Navistar Recalls International Trucks Due to Parking Brake Failure Risk

    Navistar is recalling specific International trucks because engaging the PTO switch can override the parking brake, causing unintended movement.

    Product
    INTERNATIONAL — INTERNATIONAL DURASTAR, WORKSTAR, HV, MV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V840000·2019-11-21

    Land Rover Recalls 2020 Range Rover Evoque for Headliner Plate Defect

    Jaguar Land Rover is recalling 2020 Range Rover Evoque vehicles because a metal plate on the headliner may detach during a crash, increasing injury risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V839000·2019-11-21

    Ford Recalls 2019 Rangers Due to Rear Light Connector Issues

    Ford is recalling 2019 Ranger trucks because rear light connectors may be misaligned, causing lights to fail and increasing crash risk.

    Product
    FORD — FORD RANGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20029·2019-11-21

    SCARPA Recalls Maestrale Ski Boots Due to Shell Cracking Hazard

    SCARPA is recalling Maestrale RS and Maestrale men's ski boots because the shells can crack, posing a fall hazard. No injuries have been reported.

    Product
    Maestrale RS and Maestrale Men's Ski Boots
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0356-2020·2019-11-20

    TriMed Locking Drill Guide Recall Due to Epoxy Coating Defect

    TriMed Inc. is recalling 1,042 Locking Drill Guides because the epoxy coating on the instruments can pop off.

    Product
    TriMed Locking Drill Guide, 2.3mm, REF GUIDELCBS-2.3, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0154-2020·2019-11-20

    Tony's Canned Salmon Recalled for Potential Under-Processing

    Tony's Smokehouse and Cannery is recalling 6.5 oz. cans of Columbia Gorge Salmon because the product may have been under-processed and the lot code is missing from records.

    Product
    Tony's Columbia Gorge Salmon, Skinless and boneless salmon, packaged in a metal can, Net Wt. 6.5 oz./184g. The label reads in parts: "*** Columbia Gorge Salmon *** Ingredients: Salmon and Salt ***TONY'S SMOKEHOUSE AND CANNERY 1316 Washington Street Oregon City, OR 97045…
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0369-2020·2019-11-20

    Carroll-Baccari Recalls Pedia Prep Skin Preparation Due to Contamination Risk

    Carroll-Baccari, Inc. is recalling Pedia Prep skin preparation products due to potential contamination with Burholderia cepacia. The recall affects 2,445 units distributed in the US, Canada, Spain, England, and Australia.

    Product
    Pedia Prep: MD0033T - 4 oz tubes MD0033--SUP - Single Use Cups Skin preparation used to enhance signal quality of patient recording electrodes (i.e. EKG, ECG, etc.)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0352-2020·2019-11-20

    Smiths Medical Recalls ProtectIV Plus Safety IV Catheters

    Smiths Medical is recalling certain lots of ProtectIV Plus Safety IV Catheters because the safety mechanism guard may be damaged.

    Product
    ProtectIV¿ Plus Safety IV Catheter, sterile. Packaged in a pouch and than into an inner carton.
    Category
    Medical Device
    Distribution
    21 states
  • HighFDA (Devices)·Z-0368-2020·2019-11-20

    Carroll-Baccari Lemon Prep Skin Preparation Recalled for Potential Contamination

    Carroll-Baccari, Inc. is recalling Lemon Prep skin preparation products due to potential contamination with Burholderia cepacia. The recall affects 24,979 units distributed in the US, Canada, Spain, England, and Australia.

    Product
    Lemon Prep: MD0019T - 4 oz tubes MD0019--SUP - Single Use Cups Skin preparation used to enhance signal quality of patient recording electrodes (i.e. EKG, ECG, etc.)
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0366-2020·2019-11-20

    TriMed Recalls Olecranon Hook Plates Due to Unqualified Hole Modification

    TriMed Inc. is recalling 583 Olecranon Hook Plates because angled holes may have been modified from specifications without full qualification.

    Product
    TriMed Olecranon Hook Plate, Lt, 6-Holes, REF: OHOOKL-6, Non-Sterile, RX only, (01) 00842188101281 - Product Usage: The OHOOKL is a semi-tubular design bone plate with two offset intramedullary tines, which are intended to penetrate the small terminal fragment to provide…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0404-2020·2019-11-20

    Galil Medical Recalls Visual-ICE Cryoablation Systems Due to Needle Clogging

    Galil Medical is recalling 49 Visual-ICE Cryoablation Systems because the needles may clog or fail to freeze tissue adequately.

    Product
    Visual-ICE Cryoablation System, FPRCH6000. The cryoablation system is a mobile console system intended for cryoablative tissue destruction using a minimally invasive procedure. The system is computer-controlled with a touch screen user interface that allows the user to control…
    Category
    Medical Device
    Distribution
    22 states
  • HighCPSC·20026·2019-11-20

    B&B Acquisition Recalls Wintergreen Essential Oils for Child-Resistant Packaging Failure

    B&B Acquisition is recalling Airome Wintergreen and Deep Soothe essential oils because the bottles lack child-resistant caps, posing a poisoning risk to young children.

    Product
    Airome Wintergreen Essential Oil and Deep Soothe Essential Oil 100 percent Pure & Natural Therapeutic Grade Essential Oils
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0394-2020·2019-11-20

    Orthofix Pelvis Sterile Kit Drill Bits Recalled for Design Defect

    Orthofix Srl is recalling specific lots of Pelvis Sterile Kits because the drill bits have a geometrical detail that does not match the intended design, potentially lowering cutting performance.

    Product
    ORTHOFIX Catalogue Number: ref: 99-93501, PELVIS STERILE KIT, RX ONLY, UDI: (01)18033509859908
    Category
    Medical Device
    Distribution
    29 states
  • HighFDA (Food)·F-0149-2020·2019-11-20

    Food Lion Creamy Chocolate Frosting Recalled for Undeclared Milk Allergen

    Gilster-Mary Lee Corp. is recalling Food Lion Creamy Chocolate Frosting because cream cheese frosting was mislabeled as chocolate, failing to declare the major allergen milk.

    Product
    Food Lion Creamy Chocolate Frosting, Net Wt 16 OZ, Distributed by Food Lion, LLC, Salisbury, NC, foodlion.com, packaged in 12 cans per case.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0359-2020·2019-11-20

    TriMed Wrist Hook Impactors Recalled for Rust Risk

    TriMed Inc. is recalling 561 Wrist Hook Dorsal and Volar Impactors because they can rust due to an improper manufacturing process.

    Product
    TriMed Wrist Hook Dorsal Impactor, REF IMPCT-WHD; and TriMed Wrist Hook Volar Impactor, REF IMPCT-WHV, both nonsterile, Rx, The firm name on the labels is TriMed Inc., Santa Clarita, CA.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0151-2020·2019-11-20

    Harris Teeter Ice Cream Recalled for Undeclared Soy Allergen

    Harris Teeter is recalling specific containers of Smooth & Creamy Take the Cake Ice Cream because the ingredient soy was not declared on the label.

    Product
    Harris Teeter SMOOTH & CREAMY TAKE THE CAKE ICE CREAM 1.5 QT (1.42L) container, Lower Fat, PROUDLY DISTRIBUTED BY: HARRIS TEETER, LLC, MATTHEWS, NC 28105 UPC 0 72036 98179 0
    Category
    Food
    Distribution
    3 states