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.

34026–34050 of 50502

  • HighFDA (Devices)·Z-0521-2017·2016-11-23

    ICU Medical Recalls SafeSet Reservoir Kits Due to Potential Leak

    ICU Medical is recalling 10 units of SafeSet Reservoir and blood sampling kits containing Transpac IV transducers due to a potential for leak.

    Product
    SAFESET" KIT W/03ML FLUSH DEVICE FOR HOLMES REG. M.C., Item No. 46097-30 The Transpac Disposable Straight Pressure Transducer (DSPT) is an extravascular pressure transducer that interfaces between a catheter and pressure monitor by converting changes in pressure into electrical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0523-2017·2016-11-23

    ICU Medical Recalls Transpac IV Transducer Kits Due to Leak Risk

    ICU Medical is recalling 70 units of Transpac IV transducer kits due to a potential leak in the SafeSet Reservoir system.

    Product
    QUAD TRANSDUCER KIT WITH 03ML FLUSH DEVICE FOR LUBBOCK HEART HOSP., Item No. 46097-36 The Transpac Disposable Straight Pressure Transducer (DSPT) is an extravascular pressure transducer that interfaces between a catheter and pressure monitor by converting changes in pressure…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·17714·2016-11-22

    BRP Recalls 2017 Can-Am Maverick X3 Side-by-Side Off-Road Vehicles

    BRP is recalling about 2,380 model year 2017 Can-Am Maverick X3 side-by-side off-road vehicles because a steering defect can cause loss of control and crashes.

    Product
    Side-by-side off-road vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V846000·2016-11-22

    Forest River Recalls 2017 XLR Trailers for Incorrect Federal Placard

    Forest River is recalling certain 2017 XLR Toyhauler trailers because they may have an incorrect Federal Placard that fails to indicate a third axle.

    Product
    FOREST RIVER — FOREST RIVER XLR TOYHAULER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·112-2016·2016-11-22

    Omni Custom Meats Recalls Roasted Chicken Quarters Due to Undeclared Soy Allergen

    Omni Custom Meats is recalling approximately 191,695 pounds of marinated Roasted Chicken Quarters because the product contains soy, an undeclared allergen.

    Product
    Omni Custom Meats, Inc. — Omni Custom Meats, Inc Recalls Roasted Chicken Quarters Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·16V847000·2016-11-22

    Nissan Recalls 2016 Titan XD Trucks for Fuel Tank Ventilation Defect

    Nissan is recalling 12,112 model year 2016 Titan XD diesel vehicles because a fuel tank breather tube may not be properly connected, causing inaccurate fuel gauge readings.

    Product
    NISSAN — NISSAN TITAN XD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V844000·2016-11-21

    GM Recalls 2016 Buick Cascada for Power Window Safety Standard Violation

    General Motors is recalling 2016 Buick Cascada vehicles because an incorrect roof control module may allow windows to close automatically or remotely, increasing injury risk.

    Product
    BUICK — BUICK CASCADA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V842000·2016-11-21

    Hyundai Recalls Tucson and Santa Fe for Trailer Hitch Wiring Defect

    Hyundai is recalling 2016-2017 Tucson and 2017 Santa Fe vehicles because a trailer hitch wiring malfunction may cause brake lights to stay on, confusing other drivers.

    Product
    HYUNDAI — HYUNDAI TUCSON, SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V843000·2016-11-21

    Hyundai Recalls 2007-2008 Entourage Vehicles for Hood Latch Defect

    Hyundai is recalling 2007-2008 Entourage vehicles because the secondary hood latch may corrode and fail to engage, increasing crash risk if the hood opens while driving.

    Product
    HYUNDAI — HYUNDAI ENTOURAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V838000·2016-11-18

    Navistar Recalls IC Bus CE and BE Models for Heater Hose Defect

    Navistar is recalling 157 IC Bus CE and BE transit buses because a heater hose may split, leaking hot coolant into the driver's foot area.

    Product
    IC BUS — IC BUS CE, BE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V839000·2016-11-18

    Maserati Recalls 2017 Models for Backup Camera Software Defect

    Maserati is recalling 7,481 model year 2017 Quattroporte, Ghibli, and Levante vehicles because the backup camera may disable in freezing temperatures, increasing crash risk.

    Product
    MASERATI — MASERATI QUATTROPORTE, GHIBLI, LEVANTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V837000·2016-11-18

    Navistar Recalls IC Bus School Buses Due to Heater Hose Defect

    Navistar is recalling specific IC Bus school buses because a heater hose may split, leaking hot coolant into the driver's foot area and increasing the risk of burns or crashes.

    Product
    IC BUS — IC BUS CESB, CASB, CE, BE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·108-2016·2016-11-17

    Pork Barbeque Products Recalled for Undeclared Soy Allergen

    Morty Pride Meats, Inc. is recalling about 237,891 pounds of pork barbeque products because the labels do not declare soy, an allergen present in the Worcestershire sauce used to make them. The products were sold in North Carolina and South Carolina.

    Product
    Morty Pride Meats, Inc. — Morty Pride Meats, Inc. Recalls Pork Barbeque Products Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·16V834000·2016-11-17

    Thor Motor Coach Recalls 2014-2016 Tuscany Motorhomes for Fire Risk

    Thor Motor Coach is recalling 528 Tuscany motorhomes because water leaks into the keyless entry module, causing electrical shorts that increase fire risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TUSCANY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0390-2017·2016-11-16

    Maquet Accessory Adapter Recalled Due to Head Rest Slipping Hazard

    Maquet Medical Systems USA is recalling Accessory Adapter part number 600525A0 because a head rest mounted to the device slipped out of the mounting rail.

    Product
    Accessory Adapter Part number 600525A0 Product Usage: designed for the mounting of MAQUET accessories with the dovetail guide interface immediately before, during and after surgical interventions as well as for examination and treatment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0362-2017·2016-11-16

    Hospira Symbiq Infusion Pump Recall for White Screen Safety Shutdown

    Hospira is recalling Symbiq Two Channel Infusers that may display a white screen, causing the device to stop infusion and sound an alarm, which can delay or interrupt therapy.

    Product
    Symbiq Two Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids. List number 16027. Note that Hospira retired this pump June 30, 2015. The Hospira Symbiq Infusion System is intended for the delivery of fluids, solutions, drugs, agents…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0285-2017·2016-11-16

    Koffee Kup Hamburger Buns Recalled for Plastic Contamination

    Koffee Kup Bakery is recalling hamburger buns in multiple states due to potential plastic pieces.

    Product
    Koffee Kup Hamburger Buns- White, Wheat, Seeded -3 1/2" 4", 5", packaged 16 oz. 18, oz, 20 oz, 25 oz, 29 oz
    Category
    Food
    Distribution
    12 states
  • HighFDA (Food)·F-0417-2017·2016-11-16

    Fruit 66 Tropical Punch Recalled Due to Swelling Cans

    1 Epic, LLC is recalling specific lots of Fruit 66 Tropical Punch because swelling cans may cause lids to pop off, posing an injury risk.

    Product
    Fruit 66 Tropical Punch, 8 FL OZ (240 mL) 100% Juice Non-Carbonated. Flavored 100% Juice Blend from concentrate with other natural Flavors and added Ingredients. UPC 98341-00108.
    Category
    Food
    Distribution
    14 states