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.

18126–18150 of 50404

  • HighFDA (Devices)·Z-0539-2022·2022-02-09

    DIXI Medical Depth Electrodes recalled for potential sterile packaging defect

    DIXI MEDICAL USA is recalling 461 Microdeep Depth Electrodes. The internal blister packaging may deform, potentially compromising the sterile barrier when removed from the protective Tyvek bag.

    Product
    The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or Electrode) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0542-2022·2022-02-09

    DIXI Medical Microdeep Depth Electrode packaging defect may compromise sterility

    DIXI MEDICAL USA is recalling Microdeep Depth Electrodes due to potential deformation of the internal packaging (blister pack) that could compromise the sterile barrier. The recall affects 365 units distributed nationwide.

    Product
    The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or Electrode) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0625-2022·2022-02-09

    Walla Walla Cheese Company Cheddar Curds Recalled for Under Pasteurization

    Walla Walla Cheese Company is recalling AJ's Walla Walla Sweet Onion Mustard Cheddar Curds because the cheese was made from under pasteurized milk.

    Product
    Walla Walla Cheese Company AJ s Walla Walla Sweet Onion Mustard Cheddar Curds. Keep Refrigerated. Product is packaged in vacuum sealed zip lock bags. Net wt. 10 oz.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0536-2022·2022-02-09

    DIXI Microdeep Depth Electrode packaging deformation poses sterility risk

    DIXI Medical USA is recalling 2,141 Microdeep Depth Electrodes nationwide due to potential deformation of the blister pack that could compromise the sterile barrier when devices are removed from their Tyvek bags.

    Product
    The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or Electrode) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V074000·2022-02-09

    Maintainer Recalls 2021-2022 Truck-Mounted Cranes Due to Fire Risk

    Maintainer is recalling 2021-2022 truck-mounted cranes because an incorrectly installed guard may damage fuel hoses or cables, increasing fire risk.

    Product
    MAINTAINER — MAINTAINER CRANE W/ SERVICE BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22072·2022-02-09

    Petzl Scorpio Eashook Lanyards with Carabiners Recalled for Fall Risk

    Petzl is recalling about 230 Scorpio Eashook Lanyards with Carabiners because the carabiner's automatic gate-closing system can malfunction, creating a risk of serious injury or death.

    Product
    Scorpio Eashook Lanyards with Carabiners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0548-2022·2022-02-09

    INTEGRA SURFIX ALPHA Torx 10 Screwdriver Out of Specification Recalled

    Smith & Nephew recalls INTEGRA SURFIX ALPHA Screwdriver Torx 10 units because they are out of specification and may not mate properly with the Surfix Alpha Lock screw.

    Product
    INTEGRA SURFIX ALPHA Screwdriver Torx 10, REF 219 135 ND
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0538-2022·2022-02-09

    FDA Recalls DIXI Medical Microdeep Depth Electrodes Due to Packaging Defect

    DIXI MEDICAL USA is recalling Microdeep Depth Electrodes nationwide due to potential internal packaging deformation that could compromise the device's sterile barrier.

    Product
    The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or Electrode) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22076·2022-02-09

    Escalade Sports Tennis Tables Recalled for Fall and Injury Hazards

    Escalade Sports is recalling about 5,200 tennis tables sold at Target from September to November 2021 because the table can collapse when leaned against, posing a fall hazard. The company has received 78 reports of collapse, including four reports of minor injuries.

    Product
    Escalade Sports Tennis Tables
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0630-2022·2022-02-09

    Wayfare Dairy Free Butter recalled for suspected mold growth

    WayFare Health Foods is recalling Wayfare Dairy Free Butter Salted & Whipped (610 cases) for suspected mold growth. Affected products were distributed to food distributors and consumers online across multiple states.

    Product
    Wayfare Dairy Free Butter Salted & Whipped,
    Category
    Food
    Distribution
    10 states
  • HighFDA (Devices)·Z-0547-2022·2022-02-09

    Ultrasound System Software Calculation Error in Siemens ACUSON Sequoia

    Software error in certain Siemens ACUSON Sequoia ultrasound systems causes measurement values to be overestimated, potentially resulting in patient misdiagnosis.

    Product
    ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V072000·2022-02-09

    Altec Recalls 2019-2021 Aerial Devices Due to Bolt Failure Risk

    Altec is recalling 2019-2021 ATTXX-M/P/S aerial devices because over-tightened bolts in the rotation bearing may break, risking separation of the pedestal and turntable.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0626-2022·2022-02-09

    Walla Walla Cheese Company Mad Curds Recalled for Underpasteurized Milk

    Walla Walla Cheese Company has recalled Mad Curds produced from underpasteurized milk. The product was distributed in Oregon and Washington.

    Product
    Walla Walla Cheese Company Mad Curds. Keep Refrigerated. Product is packaged in vacuum sealed zip lock bags - net wt. 5 lbs. and 10 oz.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0541-2022·2022-02-09

    DIXI Microdeep Depth Electrodes recalled for potential packaging deformation compromising sterility

    DIXI MEDICAL USA is recalling 1792 Microdeep Depth Electrodes due to potential deformation of the internal blister pack that could compromise the sterile barrier when the device is removed from its Tyvek bag.

    Product
    The DIXI Medical Microdeep Depth Electrode (Microdeep Depth Electrode or Electrode) is a smooth electrode that is 0.8 mm in diameter with a rounded (hemispherical) tip. The electrode has multiple platinum/iridium contacts that are 2 mm long, with a total exploration length…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0624-2022·2022-02-09

    Walla Walla Cheese Cheddar Curds recalled due to under-pasteurization

    Walla Walla Cheese Company is recalling Cheddar Curds due to under-pasteurization of the milk used in production, which may not eliminate potentially harmful bacteria.

    Product
    Walla Walla Cheese Company Cheddar Curds. Keep Refrigerated. Product is packaged in vacuum sealed zip lock bags. Net wt. 5 lbs.
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-0557-2022·2022-02-09

    Chameleon PTA Balloon Catheter difficult protector sleeve removal risk

    The Chameleon PTA Balloon Dilation Catheter 8 mm x 40 mm has a protector sleeve that may be difficult to remove, potentially damaging the balloon and causing patient harm. Covidien is recalling 1,994 devices.

    Product
    Chameleon PTA Balloon Dilation Catheter 8 mm x 40 mm, Chameleon PTA Balloon Catheter with Injection Port 8 mm x 40 mm; Cardiovascular. Product Numbers CH08-40-75GB and CH08-40-75US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0532-2022·2022-02-09

    Vagus Nerve Stimulation Therapy Leads Recalled for Tubing Wall Defect

    LivaNova's PerenniaDURA vagus nerve stimulation leads may have insufficient silicone tubing thickness due to a manufacturing issue. This could result in unintended stimulation delivery or loss of therapy if the tubing is breached.

    Product
    Vagus Nerve Stimulation (VNS) Therapy Leads, PerenniaDURA, Model: 303. Model 303-20 PereniaDURA Lead (2.0 mm electrode inner diameter) and Model 303-30 PereniaDURA Lead (3.0 mm electrode inner diameter)
    Category
    Medical Device
    Distribution
    7 states
  • HighCPSC·22075·2022-02-09

    Pittsburgh Automotive Pneumatic Roller Seats Recall Due to Fall Hazard

    Harbor Freight Tools is recalling Pittsburgh Automotive pneumatic roller seats because the connection between the seat and post can break, causing users to fall. The company has received 96 reports of seat welds breaking, including 10 reports of minor injuries.

    Product
    Pittsburgh Automotive Pneumatic Roller Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0554-2022·2022-02-09

    HARDY DIAGNOSTICS CatScreen diagnostic kit recalled due to improper storage

    HARDY DIAGNOSTICS CatScreen test kits (Model HADZ110) are recalled because units were stored in temperature-controlled settings instead of refrigeration. Improper storage may compromise product effectiveness.

    Product
    HARDY DIAGNOSTICS CatScreen, 25dsk/vial
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22071·2022-02-09

    Children's Nightgowns Recalled for Flammability Standards Violation

    AllMeInGeld children's nightgowns fail to meet federal flammability standards for sleepwear, posing a burn injury risk. About 3,900 units were sold on Amazon.com from October 2017 through June 2021.

    Product
    Children's Nightgowns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V068000·2022-02-08

    Tiffin motorhomes have improperly secured buss bars increasing fire risk

    Tiffin is recalling 2018-2022 Allegro and Allegro Breeze motorhomes where an improperly secured electrical buss bar can cause the DC Distribution Panel to overheat and potentially start fires. Dealers will replace the buss bar with a cable for free.

    Product
    TIFFIN — TIFFIN ALLEGRO, ALLEGRO BREEZE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V067000·2022-02-08

    Holiday House Travel Trailers Propane Regulator Failure Risk

    Holiday House is recalling certain 2019–2021 travel trailers equipped with defective Winntec propane regulators that may fail and increase propane pressure, raising fire risk in gas appliances.

    Product
    HOLIDAY HOUSE — HOLIDAY HOUSE 24TB, 27RQ, 18RB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V065000·2022-02-07

    Roadtrek Recreational Vehicles Recalled for Unattached Propane Lines

    Roadtrek is recalling certain 2021-2022 recreational vehicles because the propane line may not be attached to the water heater. An unattached propane line can allow gas to enter the vehicle, increasing the risk of a fire.

    Product
    ROADTREK — ROADTREK CHASE, ZION SRT, ZION SLUMBER, ZION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V064000·2022-02-07

    Audi Recalls 2022 Q3 Vehicles for Rearview Camera Software Error

    Audi is recalling 2022 Q3 vehicles because a software error may prevent the rearview camera from displaying an image when reversing, increasing crash risk.

    Product
    AUDI — AUDI Q3
    Category
    Vehicle
    Distribution
    Distributed nationwide