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.

41651–41675 of 50511

  • HighNHTSA·14V119000·2014-03-12

    Zero Motorcycles Recalls 2014 Models Due to Motor Rotor Contact

    Zero Motorcycles is recalling specific 2014 FX, S, DS, and SR models because the motor rotor may contact the stator, potentially causing the rear wheel to lock up and increasing crash risk.

    Product
    ZERO — ZERO S, DS, SR, FX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1082-2014·2014-03-12

    Elekta Desktop Pro Linear Accelerator Control Software Recalled for Calibration Errors

    Elekta, Inc. is recalling Desktop Pro linear accelerator control software because incorrect values may be entered during calibration procedures.

    Product
    Desktop Pro TM linear accelerator control software intended to assist a licensed practitioner in the delivery of radiation to defined target volumes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1081-2014·2014-03-12

    Elekta RT Desktop Software Recall for Calibration Input Errors

    Elekta is recalling RT Desktop software because users may enter incorrect values during calibration procedures for radiation therapy linear accelerators.

    Product
    RT Desktop The EOS RT Desktop, as with the predicate SL/SLi Series user interface, is intended to be used as the user interface for the SL/SLi Series Linear Accelerators that are used for the radiation therapy treatments of malignant neoplastic diseases, as determined by a…
    Category
    Medical Device
    Distribution
    22 states
  • HighFDA (Drugs)·D-1147-2014·2014-03-12

    Hospira Recalls Bupivacaine Hydrochloride Vials Due to Particulate Matter

    Hospira Inc. is recalling 115,500 vials of Bupivacaine Hydrochloride injection due to a confirmed report of visible particulate matter embedded in the glass vials.

    Product
    BUPIVACAINE HYDROCHLORIDE — BUPIVACAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·14129·2014-03-12

    Fitbit Recalls Force Activity-Tracking Wristband Due to Skin Irritation Risk

    Fitbit is recalling Force activity-tracking wristbands because the materials can cause skin irritation, rashes, or blistering. Consumers should contact Fitbit for a full refund.

    Product
    Wireless activity-tracking wristband
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1084-2014·2014-03-12

    Elekta Agility Software Recall for Calibration Input Errors

    Elekta is recalling Agility software version 3.0 because incorrect values can be entered during calibration procedures for medical linear accelerators.

    Product
    Agility. Version 3.0 of the Integrity interface and control software for the Elekta range of medical digital linear accelerators which is associated with Agility collimators.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1602-2014·2014-03-12

    Rise'n Roll Bakery Recalls Amish Wedding Nutty Crunch for Undeclared Peanuts

    Rise'n Roll Bakery is recalling Amish Wedding Nutty Crunch products because they contain undeclared peanuts. The recall covers products with a best-by date of June 13, 2014, or earlier.

    Product
    Amish Wedding, Nutty Crunch, ... boiled to perfection, Distributed by Troyer Cheese, Inc. ... Millersburg, OH 44654, NT. WT 8 oz., ING cashews, pecans, almonds, butter (milk) sugar. Contains Nuts and Milk. UPC Code 8 27912 04158
    Category
    Food
    Distribution
    11 states
  • HighFDA (Devices)·Z-1085-2014·2014-03-12

    Elekta Agility software recall for potential calibration input errors

    Elekta is recalling Agility software version 3.1 for linear accelerators because incorrect values could be entered during calibration procedures.

    Product
    Agility. Version 3.1 of the Integrity interface and control software for the Elekta range of medical digital linear accelerators which is associated with Agility collimators.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1134-2014·2014-03-12

    DeRoyal Circumcision Clamps Recalled for Manufacturing Defects

    DeRoyal Industries is recalling three lots of circumcision clamps that may not clamp completely at the surgical site due to manufacturing errors.

    Product
    DeRoyal ST. Circumcision Clamp, REF 32-1622, Size 1.3 cm, 1 Per Pack, Rx Only STERILE EO, distributed by DeRoyal Industries.
    Category
    Medical Device
    Distribution
    10 states
  • HighNHTSA·14V115000·2014-03-12

    Triple E Recalls 2014 Free Spirit Motorhomes Due to Obstructed Taillight

    Triple E Recreational Vehicles is recalling 2014 Free Spirit motorhomes because the spare tire carrier obstructs the driver's side taillight, increasing crash risk.

    Product
    FREE SPIRIT — FREE SPIRIT FS22, FS22TE, FS22SS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1083-2014·2014-03-12

    Elekta Integrity Software Recalled for Calibration Input Errors

    Elekta, Inc. is recalling Integrity Version 1.1 software for linear accelerators because incorrect values can be entered during calibration procedures.

    Product
    Integrity. Version 1.1 of the Integrity interface and control software for the Elekta range of medical digital linear accelerators.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1147-2014·2014-03-12

    GE Healthcare Recalls Solar 8000M/i Patient Monitors Due to AVOA Feature Failure

    GE Healthcare is recalling Solar 8000M and 8000i patient monitors because the Automatic-View-On-Alarm feature may stop functioning after a specific discharge event.

    Product
    GE Healthcare Solar 8000M and Solar 8000i Patient Monitor software version 5.4, 5.5, or 5.6 with the Automatic-View-On- Alarm (AVOA) feature enabled. The Solar 8000i with Patient Data Module / Transport Pro with Patient Data Module is intended for use under the direct…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1128-2014·2014-03-12

    Carestream Recalls Kodak 2200 Intraoral X-Ray Systems Due to Arm Failure

    Carestream Health is recalling Kodak 2200 Intraoral X-Ray Systems because the device arms may break early. This affects 347 units distributed in the US and Canada.

    Product
    Model Kodak 2200 Intraoral X-Ray System, Catalog Numbers 5303177, 5303169, 5303151, XR-5154323 -- Carestream Health, Inc. Made in France -- --- COMMON/USUAL NAME: Dental X-Ray Systems -- CLASSIFICATION NAME: Unit, X-Ray, Extraoral with timer --- There are four major…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1124-2014·2014-03-12

    Medical Information Technology Recalls MEDITECH Microbiology Calculator Module

    Medical Information Technology, Inc. is recalling MEDITECH Microbiology calculator modules due to a risk of patient results being removed from laboratory and electronic medical record systems.

    Product
    MEDITECH Microbiology - Calculator/data processing module, for clinical use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1127-2014·2014-03-12

    Carestream Recalls Kodak 2100 Intraoral X-Ray Systems Due to Arm Breakage

    Carestream Health is recalling Kodak 2100 Intraoral X-Ray Systems because the device arms may break early. The recall covers 347 units distributed in the US and Canada.

    Product
    Model Kodak 2100 Intraoral X-Ray System, Catalog Numbers 5303144, 8011579 -- Carestream Health, Inc. 150 Verona Street Rochester, NY 14608 -- Made in France -- TROPHY 77435 Marne La Vallee --- COMMON/USUAL NAME: Dental X-Ray Systems -- CLASSIFICATION NAME: Unit, X-Ray…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V114000·2014-03-11

    Mazda Recalls 2010-2012 Mazda6 Vehicles for Fuel Tank Fire Risk

    Mazda is recalling 2010-2012 Mazda6 vehicles because spider webs may block a fuel hose, causing tank cracks and fuel leaks that increase fire risk.

    Product
    MAZDA — MAZDA MAZDA6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V110000·2014-03-11

    Blue Bird Recalls 2014 School Buses for Rear Wheelhousing Joint Separation

    Blue Bird is recalling 526 model year 2014 Vision and All American school buses because a rear wheelhousing joint may have separated during manufacturing, increasing injury risk in a crash.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V121000·2014-03-11

    Winnebago Recalls Motorhomes Due to Stuck Accelerator Pedal Risk

    Winnebago is recalling 2014-2015 Travato, 2014 Trend, and 2014 Itasca Viva! motorhomes because the accelerator pedal may get stuck, increasing crash risk.

    Product
    WINNEBAGO — WINNEBAGO TRAVATO, TREND, ITASCA VIVA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V113000·2014-03-11

    Great Dane Recalls 2013-2015 Flatbed Trailers Due to Bracket Defect

    Great Dane is recalling 2013-2015 flatbed trailers because cargo restraint brackets may break, causing plates to fall and create road hazards.

    Product
    GREAT DANE — GREAT DANE FLATBED TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V109000·2014-03-10

    Honda Recalls 2014 Civic Vehicles for Tire Bead Damage

    Honda is recalling 2014 Civic LX vehicles because tire beads may have been pinched during assembly, potentially causing air loss and increasing crash risk.

    Product
    HONDA — HONDA CIVIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14720·2014-03-07

    ZLP Hornet Zip Line Trolleys Recalled Due to Fall Hazard

    ZLP Manufacturing is recalling about 2,000 Hornet zip line trolleys because a retaining pin can release, causing the trolley to fall off the line.

    Product
    LP Hornet zip line trolleys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14126·2014-03-06

    Design Ideas Recalls Rubber Ducky, Blowfish, and Splat Magnets Due to Ingestion Risk

    Design Ideas is recalling approximately 26,900 miniature magnets in the shapes of ducks, blowfish, and splats because the small magnets can detach and be swallowed by children.

    Product
    Design Ideas® and Neatlife® Rubber Ducky Magnets, and Design Idea® Blowfish and Splat Magnets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14127·2014-03-06

    Tektro USA and TRP Recall Bicycle Mechanical Disc Brake Calipers

    Tektro USA and TRP are recalling Spyre and Spyre SLC mechanical disc brake calipers because the actuator arm can over-rotate, causing brake failure and a crash hazard.

    Product
    Spyre and Spyre SLC dual-piston mechanical disc brake calipers
    Category
    Consumer Product
    Distribution
    Distributed nationwide