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.

40351–40375 of 50511

  • HighNHTSA·14V637000·2014-10-10

    Goshen Buses Recalled for Wheelchair Lift Platform Cracking Risk

    Goshen Coach is recalling certain buses because wheelchair lift platform side plates may crack, posing an injury risk to operators.

    Product
    GOSHEN — GOSHEN GCII, SENTINEL, SENTRY, PACER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V641000·2014-10-10

    Mobility Works Recalls Ford Vans with Cracking Wheelchair Lifts

    Mobility Works is recalling 834 Ford E-Series vans modified with Ricon wheelchair lifts. The platform side plates may crack, causing the lift to fall and injure the operator.

    Product
    FORD — FORD, MOBILITY WORKS E150, E250, E350, fORD E-150
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15703·2014-10-09

    Fluid Handling Recalls Low Water Cut-Off Control Units for Fire Hazard

    Fluid Handling is recalling McDonnell & Miller low water cut-off control units for hot water or steam boilers due to fire and explosion hazards.

    Product
    McDonnell & Miller Low Water Cut-Off control units for hot water or steam boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V645000·2014-10-09

    GM Recalls 2015 Chevrolet Colorado and GMC Canyon for Air Bag Wiring

    General Motors is recalling 2015 Chevrolet Colorado and GMC Canyon vehicles because incorrect driver air bag wiring may disrupt deployment timing, increasing injury risk in crashes.

    Product
    CHEVROLET — CHEVROLET, GMC COLORADO, CANYON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15704·2014-10-09

    Rejuvenation Recalls Hanging Lamps Due to Risk of Falling Injury

    Rejuvenation is recalling about 85 Haleigh Wire Dome Pendant lamps because the cord system can fail, causing the lamp to fall and pose a risk of injury.

    Product
    Hanging lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0002-2015·2014-10-08

    Siemens Ysio Max Radiographic Systems Recalled for Image Loss Risk

    Siemens is recalling Ysio Max radiographic systems because a malfunction can cause images to be lost, requiring patients to repeat examinations.

    Product
    Siemens Ysio Max system The Ysio Max is a radiographic system used in hospitals, clinics, and medical practices. Ysio Max enables radiographic and tomographic exposures of the whole body including: skull, chest, abdomen, and extremities and may be used on pediatric, adult and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2538-2014·2014-10-08

    Bar Harbor Jam Company Popover Mix Recalled for Undeclared Wheat

    Bar Harbor Jam Company is recalling Maine Old Fashioned Popover Mix because the label does not declare wheat. The product was distributed in Maine, New Hampshire, and Massachusetts.

    Product
    BAR HARBOR JAM COMPANY Maine Old Fashioned Popover Mix; Net Wt 1 lb 5 oz (624g)
    Category
    Food
    Distribution
    3 states
  • HighFDA (Food)·F-2537-2014·2014-10-08

    Bar Harbor Jam Company Recalls Blueberry Muffin Mix for Wheat Labeling

    Bar Harbor Jam Company is recalling Maine Wild Blueberry Muffin Mix because the label does not declare wheat. The product was distributed in Maine, New Hampshire, and Massachusetts.

    Product
    BAR HARBOR JAM COMPANY Maine Wild Blueberry Muffin Mix; Net Wt. 1 lb 6 oz (624 g)
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-0003-2015·2014-10-08

    Siemens AXIOM Luminos dRF Max Systems Recalled for Image Loss Risk

    Siemens is recalling AXIOM Luminos dRF Max systems due to malfunctions that cause lost images and incorrect labels, potentially leading to repeated examinations.

    Product
    Siemens AXIOM Luminos dRF Max systems The Axiom Luminos dRF is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic studies. Using a digital flat detector, it can perform a range of applications including general R/F, angiography and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0004-2015·2014-10-08

    Siemens Uroskop Omnia Max X-Ray System Recalled for Image Loss

    Siemens is recalling two Uroskop Omnia Max systems because a malfunction causes image loss and incorrect labels, leading to repeated examinations.

    Product
    Siemens Uroskop Omnia Max system The Uroskop Omnia is a solid state detector fluoroscopic X-Ray system, primarily for urological applications (functional x-ray diagnostic, endourology and minimal invasive urology/surgery). The system,, which includes a radiologic/urologic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0005-2015·2014-10-08

    Siemens Medical Imaging Systems Recalled for Image Loss and Labeling Errors

    Siemens is recalling five Luminos Agile Max systems due to malfunctions that cause image loss and incorrect labels, leading to repeated examinations.

    Product
    Siemens Luminos Agile Max system The Luminos Agile is intended to be used as a universal imaging system for radiographic and fluoroscopic studies. Using either film cassettes or a digital mobile flat detector, it can perform a range of applications including general R/F…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2737-2014·2014-10-08

    Zimmer Recalls Persona Knee System Female Screws Due to Stripping Risk

    Zimmer, Inc. is recalling 16,380 units of Persona The Personalized Knee System 2.5 mm Female Screws due to potential stripping of the hex driver when used in cortical bone.

    Product
    Persona The Personalized Knee System 2.5 mm Female Screw 48 mm Length Sterile Qty-2. Sterilized using irradiation, single use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2733-2014·2014-10-08

    Lumenis Array LaserLink Recall for Erroneous Retinal Pattern Display

    Lumenis is recalling 16 Array LaserLink laser system accessories because they may project an incorrect pattern on the retina during treatment.

    Product
    Array LaserLink, Manufactured by Lumenis, The Array" LaserLink" is a laser system accessory intended for use in the treatment of ocular pathology. " For the Posterior Segment, the Array" LaserLink" is indicated for use in Retinal Photocoagulation and Panretinal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2731-2014·2014-10-08

    Intuitive Surgical Recalls da Vinci Xi Patient Side Carts Due to Sensor Failure

    Intuitive Surgical is recalling 75 da Vinci Xi Patient Side Carts because a motor sensor failure can occur after a mid-procedure restart.

    Product
    ASSEMBLY, PATIENT SIDE CART, PS4000 used with the da Vinci Xi Surgical System. Product Usage: The Intuitive Surgical Endoscope Instrument Control System (da Vinci Surgical System, Model IS4000) is intended to assist in the accurate control of Intuitive Surgical Endoscopic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V632000·2014-10-08

    Chrysler Recalls 2014 Minivans and Wranglers for Tire Pressure Software Error

    Chrysler is recalling 2014 Town and Country, Grand Caravan, and Jeep Wrangler vehicles because a software error may prevent the tire pressure monitoring system from detecting low air pressure.

    Product
    DODGE — DODGE, JEEP, CHRYSLER GRAND CARAVAN, WRANGLER, TOWN AND COUNTRY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2713-2014·2014-10-08

    Siemens Symbia Intevo SPECT/CT Systems Recalled for Rubber Isolator Aging

    Siemens Medical Solutions is recalling 48 Symbia Intevo SPECT/CT systems because a rubber isolator may degrade over time, potentially leading to drive belt rupture.

    Product
    The Symbia Intevo series consists of the Intevo 16, Intevo 6 and Intevo 2. This manual also describes the Symbia Intevo Excel. The Symbia Intevo series integrates state-of-the-art SPECT and high quality spiral CT to provide precise attenuation correction and anatomical mapping.…
    Category
    Medical Device
    Distribution
    40 states
  • HighFDA (Devices)·Z-2738-2014·2014-10-08

    Baxter SPECTRUM Pump Recall Due to Service Technician Error

    Baxter Healthcare is recalling SPECTRUM Pumps because a service technician may not have followed established procedures between May 5 and June 3, 2014.

    Product
    SPECTRUM Pump, Model No. 35700BAX. Intended to be used for the controlled administration of intravenous fluids.
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Devices)·Z-0001-2015·2014-10-08

    Invivo Recalls Philips MRI Patient Monitoring Systems Due to Metal Debris

    Invivo is recalling 10 Philips MRI Patient Monitoring Systems because metal debris found during production could cause power failures and loss of patient monitoring.

    Product
    Philips Expression MR200 MRI Patient Monitoring System Model 866120
    Category
    Medical Device
    Distribution
    1 state
  • HighFDA (Food)·F-2536-2014·2014-10-08

    Bar Harbor Jam Company Recalls Blueberry Pancake Mix for Wheat Mislabeling

    Bar Harbor Jam Company is recalling Maine Wild Blueberry Pancake Mix because the label fails to declare wheat, posing a risk to individuals with wheat allergies.

    Product
    BAR HARBOR JAM COMPANY Maine Wild Blueberry Pancake Mix; Net Wt. 1 lb 6 oz (624 g)
    Category
    Food
    Distribution
    3 states
  • HighNHTSA·14V625000·2014-10-07

    Forest River Recalls 2014-2015 Salem and Wildwood RVs for Label Errors

    Forest River is recalling 2014-2015 Salem and Wildwood recreational vehicles because incorrect weight labels may lead to tire failure and crashes.

    Product
    FOREST RIVER — FOREST RIVER SALEM, WILDWOOD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15701·2014-10-07

    KYMCO Recalls MXU 700 ATVs Due to Fuel Tank Fire and Burn Hazards

    KYMCO is recalling approximately 540 MXU 700 ATVs from model years 2013 to 2015 because fuel tank pressure buildup can cause ruptures, fires, or burns.

    Product
    All-terrain vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V628000·2014-10-07

    Trans Tech School Buses Recalled for Wheelchair Lift Platform Cracking

    Trans Tech is recalling 188 school buses equipped with Ricon wheelchair lifts because the platform side plates may crack, posing an injury risk to operators.

    Product
    TRANS TECH — TRANS TECH STUDENT SAFETY TRANSPORT, ROADSTAR, STUDENT TRANSPORTER AERO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V622000·2014-10-06

    Micro Bird Transit Bus Recall for Wheelchair Lift Platform Cracking

    Micro Bird is recalling 2006-2014 MB II and G5 transit buses because wheelchair lift platform side plates may crack, posing an injury risk.

    Product
    MICRO BIRD — MICRO BIRD MB II TRANSIT BUS, G5 TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide