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.

32926–32950 of 50502

  • HighFDA (Devices)·Z-1397-2017·2017-03-22

    Toshiba Kalare X-ray Generator Recalled for Premature Exposure Termination

    Toshiba American Medical Systems Inc is recalling 254 Kalare DREX-KL80 X-ray generators because the system may terminate exposure prematurely during an examination.

    Product
    Toshiba Kalare DREX-KL80 X-ray generator
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V192000·2017-03-21

    Fiat 500L Recall: Powertrain Software Limits Engine Acceleration

    Chrysler is recalling 2014 Fiat 500L vehicles because incorrect Powertrain Control Module software may limit engine speed and torque, increasing crash risk.

    Product
    FIAT — FIAT 500L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V179000·2017-03-16

    2016 Smart Fortwo Recalled for Headlight Adjustment Seal Defect

    Mercedes-Benz USA is recalling 2016 Smart Fortwo vehicles because the headlight adjustment mechanism may not be properly sealed, potentially allowing improper horizontal adjustment.

    Product
    SMART — SMART FORTWO COUPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1576-2017·2017-03-15

    Stubb's Barbecue Sauce Recalled for Glass Bottle Defects

    McCormick & Co. is voluntarily recalling 18oz bottles of Stubb's Sticky Sweet BBQ Sauce due to glass defects that may cause chipped or missing glass.

    Product
    McCormick & Co., Inc., Stubbs Barbecue. 18oz Best By Date of January 17, 2020.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1573-2017·2017-03-15

    Hormel Recalls Great Shake Plus Drinks Due to Undeclared Milk

    Hormel Foods is recalling Great Shake Plus fortified nutrition drinks because they contain undeclared milk, a major food allergen.

    Product
    Great Shake Plus Fortified Nutrition, Soy Formula, Strawberry Artificially Flavored, Packaged in 4 fl oz. (118 mL). Store Frozen.
    Category
    Food
    Distribution
    35 states
  • HighFDA (Food)·F-1569-2017·2017-03-15

    Hormel Recalls Great Shake Fortified Nutrition Drinks for Undeclared Milk

    Hormel Foods is recalling Great Shake and Great Shake Plus fortified nutrition drinks due to the presence of undeclared milk.

    Product
    Great Shake Fortified Nutrition, Soy Formula, Strawberry Artificially Flavored, Packaged in 4 fl oz. (118 mL), and 6 fl oz. (177 mL). Store Frozen.
    Category
    Food
    Distribution
    35 states
  • HighFDA (Devices)·Z-1405-2017·2017-03-15

    Prism Medical A625 Manual Lifts Recalled for Premature Strap Breakage

    ErgoSafe Products is recalling 21 Prism Medical A625 manual lifts because two units had straps break prematurely during internal testing at maximum load.

    Product
    A-series lift - A625 Manual w/Load Cell & Wi-Fi, Omni Part No. 324124. Prism Medical.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1414-2017·2017-03-15

    Becton Dickinson Recalls EpiCenter Plus Software Version 6.20A

    Becton Dickinson is recalling EpiCenter Plus Microbiology Data Management System software version 6.20A because outdated translation tables may cause mis-identification of organisms.

    Product
    EpiCenter Plus Microbiology Data Management System software version 6.20A, when used in conjunction with the MALDI BioTyper System . Product Usage: The EpiCenter system is a clinical data management system designed for use with certain BD instrument systems. The EpiCenter…
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-1401-2017·2017-03-15

    Boston Scientific Recalls AngioJet Ultra 5000 A Console Foot Switches

    Boston Scientific is recalling AngioJet Ultra 5000 A Console foot switches because they may stick during use, causing the device to operate continuously and undesirably.

    Product
    AngioJet¿ Ultra 5000 A Console:Foot Switch Material number (U PN) 105650 Cardiovascular: The Console is a multiple-use device that controls the Thrombectomy Set. It drives the pump, regulates fluid inflow and outflow, provides the operator with Ultra System set-up prompts…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-1581-2017·2017-03-15

    Index Fresh Recalls Hass Avocados Due to Listeria Contamination Risk

    Index Fresh is recalling specific lots of Hass avocados because they may be contaminated with Listeria monocytogenes.

    Product
    Hass Avocado 32 1 Index Fresh- USA Hass Avocado 36 1 Index Fresh- USA Hass Avocado 40 1 Index Fresh- USA Hass Avocado 48 1 Index Fresh- USA Hass Avocado 60 1 Index Fresh- USA Hass Avocado 70 1 Index Fresh- USA
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1420-2017·2017-03-15

    Siemens IMMULITE Progesterone Test Kits Recalled for DHEA-S Interference

    Siemens is recalling IMMULITE Progesterone test kits because DHEA-S causes falsely elevated results, potentially affecting diagnosis.

    Product
    IMMULITE/ IMMULITE 1000 Progesterone; Catalog Number: LKPW1; Siemens Material Number: 10381128 Product Usage: For in vitro diagnostic use with the IMMULITE¿2000 Systems Analyzers- for the quantitative measurement of progesterone in serum, as an aid in the diagnosis and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1413-2017·2017-03-15

    Encore Medical Recalls RSP Impaction Fixtures Due to Material Wear

    Encore Medical is recalling 626 RSP Impaction Fixtures because polymer material wore off during assembly, potentially affecting the humeral stem coating.

    Product
    RSP Impaction Fixture
    Category
    Medical Device
    Distribution
    0 states
  • HighNHTSA·17V182000·2017-03-15

    Ride The Ducks Recalls Amphibious Vehicles Due to Seat Belt Defect

    Ride The Ducks International LLC is recalling 1996-2014 amphibious vehicles because driver seats and seat belts may not secure occupants in a crash.

    Product
    RIDE THE DUCKS — RIDE THE DUCKS AMPHIBIOUS VEHICLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1572-2017·2017-03-15

    Hormel Recalls Great Shake Plus Drinks for Undeclared Milk

    Hormel Foods is recalling Great Shake Plus fortified nutrition drinks because they contain undeclared milk. Consumers with this product should stop using it.

    Product
    Great Shake Plus Fortified Nutrition, Soy Formula, Chocolate Artificially Flavored, Packaged in 4 fl oz. (118 mL). Store Frozen.
    Category
    Food
    Distribution
    35 states
  • HighFDA (Food)·F-1583-2017·2017-03-15

    Index Fresh Recalls Hass Avocados Due to Listeria Contamination Risk

    Index Fresh is recalling specific lots of Hass avocados because they may be contaminated with Listeria monocytogenes.

    Product
    Hass Avocado HA LB Signature Farms 15/4 60 1- USA Hass Avocado HA LTP S 60 1 Index Fresh- USA Hass Avocado HA RPCFB 10/4 70 1 Index Fresh- USA Hass Avocado HA LTP 32 2 So Good- USA
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-1582-2017·2017-03-15

    Index Fresh Recalls Avocados Due to Listeria Contamination Risk

    Index Fresh is recalling 116 cases of Hass avocados distributed in California, Utah, and Washington because they may be contaminated with Listeria monocytogenes.

    Product
    Hass Avocado HA LTP S 40 1 Index Fresh- USA Hass Avocado HA LTP S 70 1 Index Fresh- USA Hass Avocado HA LTP S 70 1 Index Fresh- USA
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-1406-2017·2017-03-15

    Prism Medical A625 Patient Lifts Recalled for Premature Strap Failure

    Prism Medical is recalling 76 A625 patient lifts because two units had straps break prematurely during internal testing at maximum load.

    Product
    A-series lift - A625 Manual Part No. 324117. Prism Medical.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-1399-2017·2017-03-15

    Parker Medical Recalls Left Double Lumen Endobronchial Tubes

    Parker Medical is recalling specific lots of Left Double Lumen Endobronchial Tubes because the single lung isolation feature did not function as intended.

    Product
    Parker Left Double Lumen Endobronchial Tube with Parker Flex-Tip (Parker Endo-Bronch with Flex Tip). Model Numbers: H-PFTDL-28-1, H-PFTDL-32-1, H-PFTDL-35-1, H-PFTDL-37-1, H-PFTDL-39-1, H-PFTDL-41-1. The product is an endotracheal tube with a double lumen for single lung…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1571-2017·2017-03-15

    Hormel Recalls Great Shake Plus Drinks for Undeclared Milk

    Hormel Foods is recalling Great Shake and Great Shake Plus fortified nutrition drinks due to the presence of undeclared milk.

    Product
    Great Shake Plus Fortified Nutrition, Soy Formula, Vanilla Artificially Flavored, Packaged in 4 fl oz. (118 mL). Store Frozen.
    Category
    Food
    Distribution
    35 states
  • HighFDA (Food)·F-1566-2017·2017-03-15

    Private Selection Salted Caramel Chocolate Almond Pie Recalled for Allergen Mislabeling

    Legendary Baking is recalling Private Selection Salted Caramel Chocolate Almond Pie because the label failed to list eggs and almonds as ingredients.

    Product
    Private Selection, Salted Caramel Chocolate Almond Pie, NET WT 34 OZ ( 2 LB 2 OZ) 963g, UPC 1111054021. Container: In a labeled pie dome and base. Pies are distributed frozen. Some stores sell refrigerated and some sell frozen.
    Category
    Food
    Distribution
    22 states