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.

20851–20875 of 50413

  • HighNHTSA·21V167000·2021-03-11

    Jaguar Recalls 2020 F-Type Vehicles Due to ABS Software Defect

    Jaguar is recalling 2020 F-Type vehicles because a startup diagnostic check may fail, potentially disabling the Anti-Lock Brake System and Dynamic Stability Control.

    Product
    JAGUAR — JAGUAR F-TYPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V168000·2021-03-11

    Land Rover Recalls 2020 Range Rover Evoque for Knee Air Bag Defect

    Land Rover is recalling 2020 Range Rover Evoque vehicles because the left-side lower knee air bag cushion cover may come loose, potentially reducing protection in a crash.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1157-2021·2021-03-10

    BioFire Film Array BCID Panels Recalled for False Positive Risk

    BioFire Diagnostics is recalling Film Array BCID Panels due to an increased risk of false positive Pseudomonas aeruginosa results when used with specific BD BACTEC vials.

    Product
    Gram-Negative Bacteria And Associated Resistance Markers; Film Array Blood Culture Identification (BCID); Film Array BCID Panel - Product Usage: intended for use with FilmArray systems. Part No: RFIT-ASY-0126 / UDI: 00815381020086 Part No: RFIT-ASY-0127 / UDI: 00815381020093…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V152000·2021-03-10

    Daimler Recalls 2019-2020 Sprinter Vans for Brake Pedal Bolt Issue

    Daimler Vans USA is recalling 2019-2020 Mercedes-Benz and Freightliner Sprinter vans because a brake pedal bolt may detach, causing brake lights to stay on and increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 1500, SPRINTER 2500, SPRINTER 3500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1160-2021·2021-03-10

    United Imaging X-ray System Recalled for Uncommanded Motion Hazard

    Shanghai United Imaging Healthcare is recalling six X-ray systems because the tube head may move unexpectedly, posing a collision risk to patients.

    Product
    Digitial Medica X-ray Imagining System, Model: uDR 596i, RX, CE0123, UDI:(01) 06971576833023 - Product Usage: intended to used by a qualified/trained doctor or technician on both adult and pediatric subjects for taking diagnostic radiographic exposures of the skull, spinal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0327-2021·2021-03-10

    Shenandoah Growers Organic Fresh Cut Basil Recalled for Cyclospora Contamination

    Shenandoah Growers is recalling organic fresh cut basil due to possible contamination with Cyclospora. Consumers should check their pantries for affected products.

    Product
    Organic fresh cut basil packaged in plastic clamshell containers. Shenandoah Growers by Thats Tasty, 0.75 oz UPC: 7-68573-00101-4 Shenandoah Growers by Thats Tasty, 2.0 oz UPC: 7-68573-02143-2 Shenandoah Growers by Thats Tasty 4.0 oz UPC: 7-68573-00141-0 Shenandoah Growers by…
    Category
    Food
    Distribution
    10 states
  • HighFDA (Food)·F-0330-2021·2021-03-10

    Urban Remedy Organic Cacao Mocha Cold Brew Coffee Recalled for Allergen Mislabeling

    Urban Remedy is recalling 208 units of Organic Cacao Mocha Cold Brew Coffee in California due to undeclared almonds and cashews.

    Product
    Urban Remedy Organic Cacao Mocha Cold Brew Coffee; 16 FL. OZ (473 mL) UPC" 8 13377 02222 9 Ingredients: Cashew Milk (filtered water, cashew, Date syrup, Vanilla Extract, Himalayan Pink Salt) Cold Brew Coffee (filtered water, coffee bean), Cacoa Powder Contains: Cashew
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·21V157000·2021-03-10

    2021 Porsche vehicles recalled for potentially loose suspension components

    Porsche is recalling certain 2021 Taycan, 911, Cayman, Boxster, and 718 Spyder models because suspension components may not have been properly tightened and could loosen, potentially causing loss of vehicle control.

    Product
    PORSCHE — PORSCHE TAYCAN, redundant CAYMAN, redundant BOXSTER, 911
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V153000·2021-03-10

    Mercedes-Benz Sprinter Recalled for Sliding Door Lock Defect

    Daimler Vans USA is recalling 2019-2020 Mercedes-Benz Sprinter vans with optional electric sliding doors because the auxiliary lock may be the incorrect type, potentially increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 1500, SPRINTER 2500, SPRINTER 4500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E018000·2021-03-10

    Safety Belt Solutions Recalls Seat Belts Due to Heat-Treatment Defect

    Safety Belt Solutions is recalling specific seat belts because the tongues may not have been heat-treated correctly, potentially failing to restrain occupants in a crash.

    Product
    SEAT BELTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V159000·2021-03-10

    Audi passenger air bag may not deploy correctly in certain model years

    Volkswagen Group (Audi) is recalling certain 2019-2021 Audi models for defective passenger air bags that may not deploy properly during a crash. Owners should contact Audi at 1-800-253-2834 for free inspection and repair.

    Product
    AUDI — AUDI A6, A7, A6 ALLROAD, S6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1158-2021·2021-03-10

    BioFire BCID2 Panel Recalled for False Positive Pseudomonas Results

    BioFire Diagnostics is recalling BCID2 Panels due to a risk of false positive Pseudomonas aeruginosa results when used with specific BD BACTEC blood culture vials.

    Product
    BioFire BCID2 Panel; IVD, Rx Only Part No: RFIT-ASY-0147 / UDI: 00815381020338 - Product Usage: intended for use with FilmArray systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1151-2021·2021-03-10

    Baxter Recalls PrisMax Hemodialysis Tubing Due to Performance Variability

    Baxter Healthcare is recalling PrisMax System Version II hemodialysis tubing due to performance variability that may cause alarms and therapy interruptions.

    Product
    The PrisMax System Version II Hemodialysis Delivery System: Automatic Repositioning System Pump Assembly, specifically tubing, Model Numbers: a) 955626 b) 955558 c) 955701 PrisMax V2 Preventive Maintenance Kit, Product Code SC616 ARPS PUMP, Product Code SC6035 ARPS Pump…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0326-2021·2021-03-10

    Vallarta Organic Basil Recalled for Cyclospora Contamination

    Vallarta Organic LLC is recalling organic basil contaminated with Cyclospora cayetanensis. The product was distributed in Virginia.

    Product
    ALBAHACA ORGANICA/BASIL, 460 gm x Bag, 15 Bags
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0331-2021·2021-03-10

    Urban Remedy Organic Almond Maca Almond Milk Recalled for Undeclared Allergens

    Urban Remedy is recalling 111 units of Organic Almond Maca Almond Milk due to a labeling error that failed to declare almonds and cashews.

    Product
    Urban Remedy Organic Almond Maca Almond Milk; 16 FL. OZ (473 mL) UPC" 8 13377 02102 4 Ingredients: Almond Milk (filtered Water, Almond) Date Syrup, Vanilla Extract, Maca Root PowerCashew Milk (filtered water, cashew, Date syrup, Maca Root Powder, Himalayan Pink Salt. C…
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·21V156000·2021-03-10

    2021 BMW XB7, X5, and X7 Head Restraints May Detach in Crash

    BMW is recalling certain 2021 XB7, X5, and X7 vehicles because the head restraints on second-row outer seats may be an incorrect type and could detach during a crash, increasing injury risk.

    Product
    BMW — BMW XB7, X5, X7, X5 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21092·2021-03-10

    Lifetime Products Recalls 6-Foot Seminar Tables Due to Injury Risk

    Lifetime Products is recalling 6-foot seminar tables because the brace arms may fail to lock, causing the table to collapse and posing an injury risk.

    Product
    Lifetime Products 6-foot Seminar Tables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21093·2021-03-10

    Hillsdale Jennings Counter and Bar Stools Recalled for Fall Hazard

    Hillsdale Furniture is recalling Jennings counter and bar stools because the seat can break off the base, posing a fall hazard.

    Product
    Hillsdale Furniture Jennings Counter and Bar Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V161000·2021-03-10

    2019-2021 Genesis G70 Engine Compartment Fire Risk from ABS Module

    Hyundai is recalling 2019-2021 Genesis G70 vehicles because the Anti-Lock Brake System module could short-circuit and cause an engine compartment fire. Owners should park outside until the ABS module fuse is replaced.

    Product
    GENESIS — GENESIS G70
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1173-2021·2021-03-10

    Siemens Sensis Vibe Systems Recalled for Potential System Freezes

    Siemens is recalling 37 Sensis Vibe systems in the US because they may sporadically freeze during operation or idle, preventing user interaction.

    Product
    Sensis / Sensis Vibe systems with software version VD12 and equipped with HP Flex Pro-C PC. Diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies Model Numbers: Sensis Vibe Hemo 11007641 Sensis Vibe Combo 11007642 Sensis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V148000·2021-03-09

    Shyft Group Recalls 2017-2019 Utilimaster Mobile Maintenance Trucks

    Shyft Group is recalling 2017-2019 Utilimaster Mobile Maintenance Trucks equipped with a generator set because a flexible exhaust tube may tear, releasing hot gases and increasing fire risk.

    Product
    UTILIMASTER — UTILIMASTER MOBILE MAINTENANCE TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide