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.

30051–30075 of 50499

  • HighFDA (Devices)·Z-0409-2018·2018-01-31

    Smith & Nephew Taylor Spatial Frame Software Recalled for Image Inversion

    Smith & Nephew is recalling Taylor Spatial Frame software versions 5.2.5 and 5.2.6 because the software may generate inverted images of the frame during strut adjustment planning.

    Product
    Smith & Nephew Taylor Spatial Frame Website software, Catalog Number 71070401. A web-based and mobile application software component of a multilateral external fixation system that is intended for fracture fixation, fixation of long bones and for joint fusions and limb…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-0602-2018·2018-01-31

    Aveka Nutra Processing Recalls Deactivated Dry Yeast Due to Metal Contamination

    Aveka Nutra Processing is recalling specific lots of SAF PRO RELAX +YF deactivated dry yeast because the product may contain pieces of metal.

    Product
    SAF PRO RELAX +YF, Deactivated Dry Yeast, Product Code 73050, Net Wt. 50 LBS. (22.7 KG), manufactured for Lesaffre Yeast Company, Milwaukee, WI.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0606-2018·2018-01-31

    Nestle HOT POCKETS Four Cheese Pizza Snack Bites Recalled for Missing Labeling

    Nestle USA is recalling 4,200 lbs of HOT POCKETS Four Cheese Pizza Snack Bites because the product was distributed without an ingredient statement or labeling, despite containing various allergens.

    Product
    Nestle HOT POCKETS¿ FOUR CHEESE PIZZA SNACK BITES in clear plastic bags.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0399-2018·2018-01-31

    Medtronic MyCareLink Patient Monitors Recalled for Remote Monitoring Issues

    Medtronic is recalling MyCareLink Patient Monitors because patients with multiple implanted heart devices may experience missed remote monitoring notifications.

    Product
    MyCareLink Patient Monitors. It is intended for used with a compatible Medtronic patient implanted heart device. The monitor is an external electronic device that interfaces with Medtronic implanted heart devices and a telecommunications connection to transmit stored…
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-0401-2018·2018-01-31

    Sorin CP5 Centrifugal Pump Recalled for Delayed Air Bubble Detection Response

    Sorin Group is recalling CP5 Centrifugal Pumps because the automatic line closure after air bubble detection may take longer than intended.

    Product
    CP5 Centrifugal Pump, made up of the drive unit, the emergency system and the pump control panel. It used with an Electrical Remote-Controlled (ERC) tubing clamp and a bubble sensor.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0403-2018·2018-01-31

    Philips Brilliance iCT CT Systems Recalled for Software Defects

    Philips Medical Systems is recalling 559 Brilliance iCT CT systems due to software issues affecting scan functions and safety features.

    Product
    Brilliance iCT - Model 728306 Computed Tomography X-ray systems
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0400-2018·2018-01-31

    Medtronic MyCareLink Smart Patient Monitors Recalled for Remote Monitoring Issues

    Medtronic is recalling MyCareLink Smart Patient Monitors because patients with multiple implanted heart devices may experience missed remote monitoring alerts.

    Product
    MyCareLink Smart Patient Monitors. It is intended for use with a compatible Medtronic patient implanted heart device. The reader is a portable electronic device that communicates with an implanted heart device
    Category
    Medical Device
    Distribution
    11 states
  • HighNHTSA·18V083000·2018-01-30

    Thomas Built Buses Recall Fire Extinguishers Due to Clogging and Injury Risk

    Daimler Trucks North America is recalling 2002-2017 Thomas Built Buses equipped with specific Kidde fire extinguishers that may clog or detach, posing injury risks.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX, FS-65, SAF-T-LINER C2, MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V079000·2018-01-30

    Eclipse Recalls 2019 Attitude Trailers Due to Incorrect Tire Load Range

    Eclipse Recreational Vehicles is recalling 2019 Attitude trailers equipped with tires that have the incorrect load range, which may lead to tire failure and increase crash risk.

    Product
    ECLIPSE — ECLIPSE ATTITUDE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18086·2018-01-30

    Walgreens Pain and Itch Relief Cream Recalled for Packaging Safety

    Natureplex is recalling Well at Walgreens pain and itch relief cream because the packaging is not child-resistant, posing a poisoning risk to young children.

    Product
    Well at Walgreens pain and itch relief cream
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V078000·2018-01-30

    Jayco Recalls 2017 Precept Motorhomes Due to Brake Fluid Leak Risk

    Jayco is recalling 2017 Precept motorhomes because missing valve block ball plugs in the brake system may cause fluid leaks or air ingestion, increasing stopping distance.

    Product
    JAYCO — JAYCO PRECEPT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V073000·2018-01-29

    Jayco Recalls 2018 Eagle Travel Trailers for Incorrect Weight Labeling

    Jayco is recalling 2018 Eagle travel trailers because the Gross Vehicle Weight Rating label may be incorrect, potentially allowing the vehicle to be overloaded.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18085·2018-01-25

    Elkay Recalls Water Coolers and Bottle Filling Stations Due to Shock Hazard

    Elkay is recalling water coolers and bottle filling stations because internal screws can break, causing a loose grounding wire and shock hazard.

    Product
    Elkay and Halsey Taylor water coolers and bottle filling stations
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18083·2018-01-25

    VTech Recalls Infant Elephant Rattles Due to Choking Hazard

    VTech is recalling Shake & Sing Elephant Rattles because the ears can break off, posing a choking hazard to young children.

    Product
    Shake & Sing Elephant Rattles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0378-2018·2018-01-24

    Roche Recalls Automated Analyzers Due to Possible Sample Mismatch

    Roche Diagnostics is recalling 2,517 automated laboratory analyzers due to a software limitation that may cause sample mismatches.

    Product
    Brand Name: ¿ cobas c 6000 MODULAR Series System e 601 ¿ cobas c 8000 MODULAR Series System - e 602 ¿ Roche / Hitachi MODULAR Analytics Combination System Model/Catalog/Part Number: MODULAR Analytics E 170 ¿ 03022109001 ¿ 03023109973 ¿ 03739040001 ¿ 03739040692 ¿…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0389-2018·2018-01-24

    Philips Brilliance 64 CT Scanner Recalled for Fastener Torque Issues

    Philips is recalling one Brilliance 64 CT scanner because certain fasteners may not be torqued to specification, posing a potential risk of harm if parts become loose.

    Product
    Brilliance 64, (Code 728231) Intended to produce images of the head and body by computer reconstruction of x-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    0 states