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.

27801–27825 of 50462

  • HighCPSC·18219·2018-09-11

    Jimco Recalls Bistro Chairs Due to Seat Breakage and Fall Hazard

    Jimco is recalling about 16,000 outdoor folding bistro chairs because the seats can break, posing a fall hazard. Consumers should stop using the chairs and contact the company for a refund.

    Product
    Bistro chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V613000·2018-09-11

    Ferrara Recalls 2017-2019 Emergency Vehicles for Brake Light Defect

    Ferrara is recalling 2017-2019 emergency vehicles because Whelen accessory brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.

    Product
    FERRARA — FERRARA INTRUDER, CINDER, ULTRA, IGNITER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18218·2018-09-11

    BlueStar and Big Chill Gas Ranges Recalled for Burn Hazard

    Prizer-Painter Stove Works is recalling BlueStar and Big Chill gas ranges and wall ovens because the convection fan can cause gas ignition and burns.

    Product
    BlueStar and Big Chill gas ranges and wall ovens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V606000·2018-09-11

    E-One Recalls 2017-2019 Emergency Vehicles Due to Brake Light Wiring Defect

    E-One is recalling 2017-2019 Typhoon, Cyclone II, and Quest II emergency vehicles because Whelen accessory brake lights may illuminate without the brake pedal being pressed.

    Product
    E-ONE — E-ONE TYPHOON, CYCLONE II, QUEST II
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V609000·2018-09-11

    Mercedes-Benz Recalls 2018 AMG E63S Due to Seat Adjustment Defect

    Mercedes-Benz is recalling 2018 AMG E63S vehicles because the front passenger seat may adjust beyond its intended limit, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG E63S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V592000·2018-09-10

    Ford Recalls 120V Charge Cords for Fire Risk

    Ford is recalling 120V convenience charge cords for 2012-2015 C-Max, Fusion, and Focus Electric vehicles because they lack thermistors, creating a fire risk.

    Product
    FORD — FORD FUSION HYBRID, FOCUS ELECTRIC, C-MAX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V603000·2018-09-10

    Turtle Top Transit Buses Recalled for Wheelchair Lift Cam Failure

    Turtle Top is recalling 2013-2018 Odyssey, VanTerra, and Terra Transit buses because a wheelchair lift cam may fail, allowing the platform to rise too high.

    Product
    TURTLE TOP — TURTLE TOP VANTERRA, ODYSSEY, TERRA TRANSIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V602000·2018-09-08

    REV Recalls 2017-2018 Ambulances with Whelen Brake Light Wiring Defect

    REV Ambulance Group is recalling 2017-2018 ambulances equipped with Whelen accessory brake lights that may illuminate without the brake pedal being pressed.

    Product
    MARQUE — MARQUE, MCCOY MILLER, ROAD RESCUE TYPE III, TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V586000·2018-09-07

    GM Recalls 2015 SUVs and Trucks for Electric Power Steering Software Issue

    General Motors is recalling 2015 Chevrolet, GMC, and Cadillac vehicles because electric power steering assist may momentarily be lost and then suddenly return, increasing crash risk.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE, TAHOE, SUBURBAN, YUKON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V594000·2018-09-07

    AEV Traumahawk Ambulances Recalled for Brake Light Wiring Defect

    Halcore Group is recalling 2017-2018 AEV Traumahawk ambulances because Whelen accessory brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.

    Product
    AEV — AEV TRAUMAHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V593000·2018-09-06

    Nissan Recalls 2019 Infiniti QX50 for Knee Air Bag Cover Defect

    Nissan is recalling 2019 Infiniti QX50 vehicles because the passenger-side knee air bag cover may separate unexpectedly in cold crashes, increasing injury risk.

    Product
    INFINITI — INFINITI QX50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1913-2018·2018-09-05

    Howard Calcagno Farms Recalls Spinach Due to Cyclospora Contamination Risk

    Howard Calcagno Farms is recalling spinach shipped in cardboard boxes labeled with the firm's name in Aurora, Oregon, due to a potential for contamination with Cyclospora cayetanensis.

    Product
    Spinach was shipped in card board boxes that are labeled with the firm name "Howard Calcagno, Aurora, OR 97002".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2937-2018·2018-09-05

    MedComp Duo-Flow XTP Straight Full Set Recalled for Suture Wing Cracking

    Medical Components, Inc. is recalling Duo-Flow XTP Straight Full Sets because suture wings may crack or break, posing risks of catheter dislocation, bleeding, and air emboli.

    Product
    Duo-Flow XTP Straight Full Set, RMS02105 RMS02108
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1921-2018·2018-09-05

    Howard Calcagno Farms Recalls Italian Parsley Due to Cyclospora Contamination Risk

    Howard Calcagno Farms is recalling 5 dozen of Italian parsley shipped in Oregon due to a potential for contamination with Cyclospora cayetanensis.

    Product
    Italian Parsley was shipped in card board boxes that are labeled with the firm name "Howard Calcagno, Aurora, OR 97002".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1916-2018·2018-09-05

    Howard Calcagno Farms Recalls Red Leaf Lettuce Due to Cyclospora Risk

    Howard Calcagno Farms is recalling Red Leaf Lettuce shipped in Oregon due to a potential for contamination with Cyclospora cayetanensis.

    Product
    Red Leaf Lettuce was shipped in card board boxes that are labeled with the firm name "Howard Calcagno, Aurora, OR 97002".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2947-2018·2018-09-05

    Civco Needle Guide Recall Due to Missing or Inadequate Adhesive

    Civco Medical Instruments is recalling 3 units of CIVCO Needle Guides because missing or inadequate adhesive may fail to hold the cannula in place.

    Product
    CIVCO Needle Guide, REF 676-150, QTY 24, STERILE EO
    Category
    Medical Device
    Distribution
    0 states
  • HighFDA (Food)·F-1917-2018·2018-09-05

    Howard Calcagno Farms Recalls Romaine Lettuce Due to Cyclospora Risk

    Howard Calcagno Farms is recalling romaine lettuce shipped in boxes labeled with the firm name in Aurora, Oregon, due to potential Cyclospora cayetanensis contamination.

    Product
    Romaine Lettuce was shipped in card board boxes that are labeled with the firm name "Howard Calcagno, Aurora, OR 97002".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1927-2018·2018-09-05

    Howard Calcagno Farms Recalls Dill for Potential Cyclospora Contamination

    Howard Calcagno Farms is recalling dill due to a potential for contamination with Cyclospora cayetanensis. The product was distributed in Oregon.

    Product
    Dill was shipped in card board boxes that are labeled with the firm name "Howard Calcagno, Aurora, OR 97002".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2958-2018·2018-09-05

    FDA Recalls Li-ion Battery Packs for BIS Monitoring Systems

    The FDA is recalling Li-ion battery packs used in BIS Vista and BIS View Monitoring Systems due to a Class II safety issue.

    Product
    Li-ion battery packs used in BIS Vista and BIS View Monitoring Systems. Product Number/CFN: 186-0208 UDI-Device Identifier (GTIN/UPN): 10884521130319
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1923-2018·2018-09-05

    Howard Calcagno Farms Recalls Red Chard Due to Cyclospora Contamination Risk

    Howard Calcagno Farms is recalling Red Chard shipped in boxes labeled with the firm's name in Aurora, Oregon, due to potential contamination with Cyclospora cayetanensis.

    Product
    Red Chard was shipped in card board boxes that are labeled with the firm name "Howard Calcagno, Aurora, OR 97002".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Food)·F-1925-2018·2018-09-05

    Howard Calcagno Farms Recalls Bright Light Chard Due to Cyclospora Risk

    Howard Calcagno Farms is recalling Bright Light Chard due to a potential for contamination with Cyclospora cayetanensis. The product was distributed in Oregon.

    Product
    Bright Light Chard was shipped in card board boxes that are labeled with the firm name "Howard Calcagno, Aurora, OR 97002".
    Category
    Food
    Distribution
    1 state
  • HighFDA (Devices)·Z-2955-2018·2018-09-05

    GE Carestation 30 Anesthesia Systems Recalled for Gas Switch Defect

    GE Medical Systems is recalling 252 Carestation 30 anesthesia systems worldwide because a gas switch may unexpectedly change position, potentially causing hypoxia.

    Product
    GE Carestation 30 anesthesia systems
    Category
    Medical Device
    Distribution
    0 states