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.

35251–35275 of 50504

  • HighNHTSA·16V526000·2016-07-11

    Honda Recalls 2016 Civic 2-Door Vehicles for Taillight Defect

    Honda is recalling 2016 Civic 2-Door vehicles because a damaged circuit board may cause side marker lights to fail, reducing visibility.

    Product
    HONDA — HONDA CIVIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V523000·2016-07-11

    MANAC Recalls 2016-2018 Trailers Due to Spring Brake Valve Defect

    MANAC is recalling 2016 Flatbed and 2017-2018 Van trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.

    Product
    MANAC — MANAC VAN TRAILER, FLATBED
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V519000·2016-07-08

    Audi Recalls 2017 Q7 Models Due to Air Bag Software Defect

    Volkswagen is recalling 2017 Audi Q7 vehicles because a software issue may cause frontal air bags to deploy with excessive force, increasing injury risk.

    Product
    AUDI — AUDI Q7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V518000·2016-07-08

    GM Recalls 2014-2016 Chevrolet SS and Caprice for Seat Belt Defect

    General Motors is recalling 2014-2016 Chevrolet SS and Caprice Police Pursuit vehicles because the driver's seat belt tensioner cable may separate, increasing injury risk in a crash.

    Product
    CHEVROLET — CHEVROLET CHEVEROLET SS, CAPRICE POLICE PURSUIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V520000·2016-07-08

    Porsche Recalls 2015 918 Spyder Vehicles Due to Seat Belt Bolt Issue

    Porsche is recalling 306 model year 2015 918 Spyder vehicles because incorrect screws may have been used on seat belt mounts, increasing injury risk in a crash.

    Product
    PORSCHE — PORSCHE 918 SPYDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V513000·2016-07-07

    Renegade Vienna and Villagio Recalled for Valve Stem Air Leak Risk

    Kibbi is recalling 2014-2016 Renegade Vienna and Villagio vehicles because valve stem extensions may loosen, causing slow air leaks and increasing the risk of tire failure and a crash.

    Product
    RENEGADE — RENEGADE VILLAGIO, VIENNA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V514000·2016-07-07

    Jayco Recalls 2017 Jay Flight SLX Travel Trailers for Incorrect Weight Labels

    Jayco is recalling 32 model year 2017 Jay Flight SLX travel trailers because incorrect weight labels may allow operators to overload the vehicle, increasing crash risk.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FLIGHT SLX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V515000·2016-07-07

    Lodi Recalls 2013-2016 Dominator Trucks Due to Crane Cover Defect

    Lodi is recalling 2013-2016 Dominator trucks with IMT cranes because a valve bank cover may crack and fall off, creating a road hazard.

    Product
    LODI — LODI DOMINATOR-PROPANE, DOMINATOR IV, DOMINATOR II, DOMINATOR III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16221·2016-07-07

    Kawasaki Recalls Mule Pro Side-by-Side Vehicles Due to Floor Cover Injury Risk

    Kawasaki is recalling about 25,000 Mule Pro side-by-side vehicles because the front floor cover can be punctured by foreign objects, posing an injury hazard to riders.

    Product
    Mule Pro side-by-side recreational off-highway vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·16216·2016-07-06

    Keenford Recalls iMoto Hoverboards Due to Fire and Explosion Risks

    Keenford Limited is recalling about 84,000 iMoto self-balancing scooters because their lithium-ion batteries can overheat, smoke, catch fire, or explode.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2064-2016·2016-07-06

    CareFusion Alaris System PC Unit Recall for Incorrect Patient Weight Data

    CareFusion 303, Inc. is recalling 69,693 Alaris System PC Units because the RESTORE feature may incorrectly populate patient weight for specific infusion modules.

    Product
    Alaris System PC Unit Model 8015 with software versions 9.17 and 9.19; Central programming, monitoring and power supply component for the Alaris System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2053-2016·2016-07-06

    Nephron Recalls Sodium Chloride Inhalation Solution Due to Sterility Concerns

    Nephron Pharmaceuticals is recalling 11,208 cartons of Sodium Chloride Inhalation Solution because internal dye tests failed to confirm vial integrity.

    Product
    Sodium Chloride Inhalation Solution, USP 3%, 60 x 4 mL Sterile Unit-Dose Vials per carton, Rx Only, NDC 0487-9003-60. A vial contains sterile, preservation-free, clear, colorless, aqueous solution as labeled for induction of sputum production where specimen collection is…
    Category
    Medical Device
    Distribution
    36 states
  • HighFDA (Devices)·Z-2056-2016·2016-07-06

    Hospira Symbiq Infusion Pumps Recalled for False Occlusion Alarms

    Hospira is recalling Symbiq Two Channel Infusers due to frequent false occlusion alarms that may delay or interrupt patient therapy.

    Product
    Symbiq Two Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids Device is a general purpose infusion pump designed to deliver fluids, solutions, medications, agents, nutritionals, electrolytes, blood and blood products for parenteral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16217·2016-07-06

    Hype Wireless Recalls Self-Balancing Scooters Due to Fire Hazard

    Hype Wireless is recalling about 25,000 Roam brand self-balancing scooters because their lithium-ion batteries can overheat, posing a risk of smoking, fire, or explosion.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2092-2016·2016-07-06

    Smith & Nephew Legion Hinge Knee Femoral Assembly Recall

    Smith & Nephew is recalling Legion Hinge Knee femoral assemblies because the cement application surface is below specification.

    Product
    LEGION(TM) HK FEMORAL ASSEMBLY, SIZE 4 LEFT, A/P 58.5 MM, M/L 66 MM, REF 71421374 The LEGION Hinge Knee System is indicated for: 1. Rheumatoid arthritis. 2. Post-traumatic arthritis, osteoarthritis, or degenerative arthritis in older patients whose age, weight and activity…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2104-2016·2016-07-06

    Medical Depot Recalls Aluminum Crutches Due to Tip Failure

    Medical Depot Inc. is recalling 123,125 pairs of Universal Quick Adjust aluminum crutches because the metal tips may fail and detach from the ground.

    Product
    Universal Quick Adjust under the following labels: 1) Aluminum crutch, adult, 1 pair per case, 2) Aluminum crutch, tall adult, 1 pair per case Aid the user in walking while relieving weight from one foot or leg.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16208·2016-07-06

    PTX Performance Products Recalls Airwalk Hoverboards Due to Fire Hazard

    PTX Performance Products is recalling about 4,900 Airwalk self-balancing scooters because the lithium-ion batteries can overheat, posing a risk of fire or explosion.

    Product
    Self-balancing scooters/hoverboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2069-2016·2016-07-06

    Pentax Confocal GI Scope Recall Due to Lodged Accessories

    Pentax Medical is recalling 17 Confocal GI Scopes because operational and therapeutic accessories can become lodged in the instrument channel.

    Product
    Confocal GI Scope Intended to provide optical visualization of an therapeutic access to the Gastrointestinal Tract. This anatomy includes, but is not restricted to, the organs, tissues and subsystems: Esophagus, Stomach and Duodenum, and Large Bowel to the Cecum. The instrument…
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-1591-2016·2016-07-06

    Eban's BAKEHOUSE Crispy Pecan Shortbread Cookies Recalled for Coconut Allergen Mislabeling

    Eban Bakery is recalling Crispy Pecan Shortbread Cookies because the label failed to list coconut in the 'Contains' section, despite it being in the ingredients.

    Product
    Product is labeled as "eban's BAKEHOUSE CRISPY PECAN SHORTBREAD COOKIES Net Weight 8.5 oz (241g) " . The cookies are packaged 6 per container. The container is a plastic tub with lid and tamper proof band.
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2085-2016·2016-07-06

    Medtronic Recalls Sagittal Saw Devices Due to Potential Fluid Leakage

    Medtronic is recalling 368 Sagittal Saw devices because testing identified a potential for fluid leakage into the motor during use.

    Product
    Saw Sagittal Catalog Number: ES 300; Saw Sagittal Refurbished Catalog Number: ES300-R; Saw Saggital, Finger Catalog Number: ES310; Saw Saggital, Finger Refurbished Catalog Number: ES310-R; Used to dissect bone in surgical applications.
    Category
    Medical Device
    Distribution
    20 states