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.

37526–37550 of 50506

  • HighFDA (Devices)·Z-2822-2015·2015-10-07

    MicroAire LipoTower Recalled for Potential Electrical Shock Hazard

    MicroAire Surgical Instruments is recalling 168 LipoTower units due to a risk of electrical shock if internal lead wires detach and the ground connection fails.

    Product
    ASP-1021 LipoTower with Aspiration Pump and Tumescent Pump. Medical use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2826-2015·2015-10-07

    Ferno iNX Wheeled Stretcher Recalled for Telescoping Load Frame Defect

    Ferno-Washington Inc is recalling 72 Ferno iNX Wheeled Stretchers because hole elongation in the load frame may allow the retention pin to move.

    Product
    Ferno iNX Wheeled Stretcher, Integrated Patient Transport & Loading System Product Usage: Stretcher for pre-hospital patient transport.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2821-2015·2015-10-07

    MicroAire LipoTower Recall Due to Electrical Shock Risk

    MicroAire Surgical Instruments is recalling three LipoTower units with aspiration pumps due to a potential risk of electrical shock if internal lead wires detach.

    Product
    ASP-1020 LipoTower with Aspiration Pump. Medical use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V626000·2015-10-06

    Kia Recalls 2011-2013 Sorento for Brake-Shift Interlock Defect

    Kia is recalling 2011-2013 Sorento vehicles because the brake-shift interlock may fail, allowing the car to roll out of Park without the brake being pressed.

    Product
    KIA — KIA SORENTO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E083000·2015-10-06

    Meritor Recalls Axles Due to Loose Caliper Bolts

    Meritor is recalling specific axle assemblies because caliper bolts may not be properly tightened. This defect could cause the caliper to detach, reducing braking performance and increasing crash risk.

    Product
    SERVICE BRAKES, AIR:DISC:CALIPER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E081000·2015-10-05

    Hale K Gearboxes Recalled for Shifting Out of Gear in Fire Apparatus

    Hale Products Inc. is recalling K Gearboxes used in fire apparatus that may shift from road to neutral while in transit, potentially increasing crash risk.

    Product
    POWER TRAIN:MANUAL TRANSMISSION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V623000·2015-10-05

    Daimler Recalls 2016 Thomas Built Buses Due to Engine Stalling Risk

    Daimler Trucks North America is recalling 2016 Thomas Built Bus Saf-T-Liner C2 school buses because the engine control module may short circuit, causing the engine to stall without warning.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16001·2015-10-01

    Pier 1 Imports Recalls Katerina Outdoor Patio Swivel Armchairs

    Pier 1 Imports is recalling Katerina outdoor patio swivel armchairs because they can tip backward while rocking, posing a fall hazard.

    Product
    Katerina Swivel Armchairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2813-2015·2015-09-30

    Siemens RAPIDPoint 500 Lactate Cartridges Recalled for Sodium Bias

    Siemens is recalling RAPIDPoint 500 Lactate Cartridges due to a negative sodium bias that affects quality control and patient results.

    Product
    Siemens RAPIDPoint 500 Measurement Cartridge Lactate (750 tests) Part Number: 10491449 Product Usage: The RAPIDPoint 500 system is designed for professional use in a point-of-care or laboratory environment. This system tests blood gases, electrolytes, metabolites, total…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3239-2015·2015-09-30

    Hillside Quickie Too Recalls Tofu Sandwiches Due to Undeclared Wheat

    Hillside Quickie Too is recalling New York Deli Tofu sandwiches in Washington because the product contains wheat but the label does not declare it.

    Product
    New York Deli Tofu is is tofu sandwich on bread or a bun, enclosed in a clam shell with label
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-3241-2015·2015-09-30

    Hillside Quickie Too Recalls Jamaican Spice Tempeh Sandwiches for Allergen Mislabeling

    Hillside Quickie Too is recalling Jamaican Spice Tempeh sandwiches because the wheat bun was not listed in the 'Contains' allergen statement, posing a risk to consumers with wheat allergies.

    Product
    Jamaican Spice Tempeh is tofu sandwich on bread or a bun, enclosed in a clam shell with label
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2798-2015·2015-09-30

    Regard Custom Surgical Pack Recalled Due to Chemical Contamination and Sterility Concerns

    Resource Optimization & Innovation Llc is recalling 24 Regard Custom Surgical Packs because they may contain chemically contaminated scrub products and lack sterility assurance.

    Product
    Regard Custom Surgical Pack, Item Number: 800628; Sterile, CV0805 - CABG B. Used in cardiovascular surgical procedures.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-2790-2015·2015-09-30

    Terumo Custom Cardiovascular Procedure Kits Recalled for Defective Hemoconcentrator Component

    Terumo is recalling 15 custom cardiovascular procedure kits because they contain recalled Medivators HPH700 High Performance Hemoconcentrators.

    Product
    Terumo Custom Cardiovascular Procedure Kit X-Coated Perfusion Pack P/N: 74077-01 Terumo Cardiovascular Procedure Kits are manufactured and customized to the design and specifications of the purchaser and/or the purchaser's principal technical representative for the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V614000·2015-09-30

    Ford Recalls 2015 F-150 Trucks for Adaptive Cruise Control Defect

    Ford is recalling 2015 F-150 trucks equipped with Adaptive Cruise Control because the system may falsely detect obstacles and brake unexpectedly, increasing crash risk.

    Product
    FORD — FORD F-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-3243-2015·2015-09-30

    Hillside Quickie Too Tofustrami Recalled for Allergen Mislabeling

    Hillside Quickie Too is recalling Tofustrami sandwiches because the wheat bun ingredient was not listed in the allergen statement.

    Product
    Tofustrami is tofu sandwich on bread or a bun, enclosed in a clam shell with label
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2794-2015·2015-09-30

    Synthes Dynamic Locking Screw System Recalled for Pin Breakage

    Synthes (USA) Products LLC is recalling Dynamic Locking Screw Systems due to pin breakage during implant removal. This notice extends to additional consignees identified after a previous recall.

    Product
    Dynamic Locking Screw System (DLS) 3.7mm & Dynamic Locking Screw (DLS) 5.0mm; intended for use in long bone fractures, the fixation of osteopenic bone, the fixation of osteotomies, and for the fixation of non-unions and malunions.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2814-2015·2015-09-30

    Siemens RAPIDPoint 500 Lactate Cartridges Recalled for Sodium Bias

    Siemens is recalling 1,213 RAPIDPoint 500 Lactate cartridges due to a negative sodium bias that affects quality control and patient results.

    Product
    Siemens RAPIDPoint 500 Measurement Cartridge Lactate (400) tests Part Number: 10491448 Product Usage: The RAPIDPoint 500 system is designed for professional use in a point-of-care or laboratory environment. This system tests blood gases, electrolytes, metabolites, total…
    Category
    Medical Device
    Distribution
    Distributed nationwide