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.

33676–33700 of 50502

  • HighNHTSA·16V905000·2016-12-15

    Jayco Recalls 2016 Alante and Precept Motorhomes for Step Wiring Defect

    Jayco is recalling 2016 Alante and Precept motorhomes because incorrectly installed entrance step wiring may cause the steps to retract unexpectedly, posing a fall risk.

    Product
    JAYCO — JAYCO ALANTE, PRECEPT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V904000·2016-12-15

    AEV Traumahawk Ambulances Recalled for Cot Mount Attachment Defect

    Halcore Group is recalling 2016 AEV Traumahawk ambulances because Stryker Medical Performance cot mounts may not securely attach the cot, posing a risk of serious injury.

    Product
    AEV — AEV TRAUMAHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E094000·2016-12-15

    Autoliv Recalls Seatbelt Pretensioners Due to Detachment Risk

    Autoliv is recalling specific seatbelt retractors because a subcomponent may detach after deployment, creating a projectile hazard inside the vehicle.

    Product
    SEAT BELTS:PRETENSIONER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V903000·2016-12-15

    Mercedes-Benz Recalls SUVs for Front Passenger Air Bag Defect

    Mercedes-Benz is recalling specific 2016-2017 SUVs because the front passenger air bag may not deploy due to a calibration error.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLE63, AMG GLS63, GL350, GL550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V897000·2016-12-14

    Triple E Recalls 2017 Serenity S24CB RVs Due to Wiring Fire Risk

    Triple E is recalling 18 model year 2017 Serenity S24CB recreational vehicles because an incorrectly connected circuit wire poses a fire risk.

    Product
    TRIPLE E — TRIPLE E SERENITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0723-2017·2016-12-14

    Siemens ADVIA 560 Hematology Systems Recalled for Incorrect Results

    Siemens is recalling ADVIA 560 Hematology Systems because a database issue may cause multiple discordant records to be generated for the same sample, leading to incorrect results.

    Product
    ADVIA 560 Hematology Systems, Siemens Material Number (SMN) 11170842, IVD.
    Category
    Medical Device
    Distribution
    13 states
  • HighNHTSA·16V898000·2016-12-14

    KZRV Recalls 2016-2017 Durango and Venom Trailers for Door Hinge Defect

    KZRV is recalling 2016-2017 Durango and Venom trailers because rear cargo door hinges may have insufficient welds, causing the door to swing down with excessive force.

    Product
    KZRV — KZRV DURANGO, VENOM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0614-2017·2016-12-14

    Handy Seafood Recalls Blue Crab Cake Mini for Undeclared Allergens

    Handy Seafood is recalling Blue Crab Cake Mini products because milk and anchovies were not declared in the allergen statement on the packaging.

    Product
    Handy Seafood, Blue Crab Cake Mini, Mini Crab Cakes, 0.5oz per Cake/12 Cakes per Tray, Skin Packed Tray, 12 Trays per Case, 2 Year Shelf Life, Best By Nov 9, 2018.
    Category
    Food
    Distribution
    5 states
  • HighFDA (Drugs)·D-0176-2017·2016-12-14

    North American Rescue Recalls Range Trauma Kits Due to Sterility Concerns

    North American Rescue is recalling specific Range Trauma Kits because the manufacturer has concerns about the sterility of the included eye wash solution.

    Product
    Range Trauma Kit ORG - Product Code 80-0213, 80-0299, 80-0298, North American Rescue
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0588-2017·2016-12-14

    Pastian's Bakery Recalls French Bread for Undeclared Wheat Allergen

    Pastian's Bakery is recalling 50 loaves of French Bread due to undeclared wheat allergen. The product was distributed only in New Mexico.

    Product
    1 1/2 French Bread. 1lb. 8 oz.. Clear Plastic Bag. 1 loaf
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-0674-2017·2016-12-14

    Plush Puffs Marshmallows Recalled for Undeclared Milk Allergen

    To Your Heart's Content is recalling Plush Puffs Marshmallows in Toasty Coconut flavor because the product contains undeclared milk.

    Product
    Plush Puffs Marshmallows Toasty Coconut 4oz. and 2lb bulk bag
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0587-2017·2016-12-14

    Pastian's Bakery Recalls Sourdough Bread for Undeclared Wheat Allergen

    Pastian's Bakery is voluntarily recalling Extra Sourdough Bread due to an undeclared wheat allergen. The product was distributed only in New Mexico.

    Product
    Extra Sourdough Bread-2 Squares. 32 oz. Clear Plastic Bag. 1 loaf
    Category
    Food
    Distribution
    1 state
  • HighNHTSA·16E093000·2016-12-14

    MORryde Recalls Zero G Ramp Door Hinges Due to Insufficient Welds

    MORryde is recalling approximately 2,500 Zero G Ramp Door hinges manufactured between August 21, 2016, and December 12, 2016, because insufficient welds may cause the door to swing down with excessive force.

    Product
    STRUCTURE:BODY:DOOR:HINGE AND ATTACHMENTS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0707-2017·2016-12-14

    Merge Healthcare Recalls eFilm Workstation Software Due to Measurement Errors

    Merge Healthcare is recalling eFilm Workstation software versions 2.1 through 4.1 because RF projection images may display incorrect measurements without a calibration indicator.

    Product
    Merge, eFilm Workstation and eFilm Lite eFilm Workstation with Modules is a software application that is used for viewing medical images. eFilm Workstation with Modules receives digital images and data from various sources (including but not limited to CT, MR, US, RF units…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0599-2017·2016-12-14

    Seely Family Farm Spearmint Candy Canes Recalled for Undeclared Soy

    Seely Family Farm is recalling spearmint candy canes due to undeclared soy lecithin. The product was distributed in Washington state.

    Product
    Spearmint candy canes, Net wt. 1.4 oz. The UPC is 8 54502 00321 8
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-0721-2017·2016-12-14

    RayStation Radiation Therapy Software Recalled for Dose Calculation Errors

    RaySearch Laboratories is recalling RayStation software versions 4.0, 4.5, 4.7, and 5.0 due to potential inaccuracies in proton dose calculations for specific treatment plans.

    Product
    RayStation 4.0, 4.5, 4.7 and 5.0; Radiation Therapy Treatment Planning System Product Usage: RayStation is a software system designed for treatment planning and analysis of radiation therapy. The treatment plans provide treatment unit set-up parameters and estimates of dose…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0680-2017·2016-12-14

    Olympus Vanta Analytical X-Ray System Recalled for Unintentional Emission Risk

    Olympus is recalling 41 Vanta Analytical X-Ray Systems due to a risk of unintentional x-ray emission if users attempt to terminate the sequence early.

    Product
    Olympus Scientific Solutions Americas Corporation (OSSA) Model: VANTA Analytical X-Ray System
    Category
    Medical Device
    Distribution
    16 states
  • HighFDA (Devices)·Z-0693-2017·2016-12-14

    Philips Brilliance 64 CT Systems Recalled for Software Error

    Philips Medical Systems is recalling 184 Brilliance 64 CT systems worldwide due to a software error involving the filament on timer.

    Product
    Brilliance 64 728231 Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysis and display equipment, patient and…
    Category
    Medical Device
    Distribution
    46 states
  • HighNHTSA·16V896000·2016-12-14

    DRV Recalls 2017 Full House Trailers Due to Door Hinge Weld Defect

    DRV Suites is recalling 2017 Full House recreational trailers because rear cargo door hinge welds may be insufficient, causing the door to swing down with excessive force.

    Product
    DRV — DRV FULL HOUSE
    Category
    Vehicle
    Distribution
    Distributed nationwide