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.

27776–27800 of 50462

  • HighFDA (Devices)·Z-2988-2018·2018-09-12

    GE Vivid E95 Ultrasound System Recalled for Power Cord Shock Risk

    GE Medical Systems is recalling 12,426 Vivid E95 ultrasound systems because the power cord may break and expose electrical conductors, creating a shock hazard.

    Product
    GE Vivid E95 ultrasound system Product The device is intended for use by a qualified physician for ultrasound evaluation of Fetal; Abdominal (including renal and GYN); Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1942-2018·2018-09-12

    Caito Foods Recalls Vegetable Garden Salad Due to Cyclospora Contamination

    Caito Foods LLC is recalling Delish Vegetable Garden Salad because an ingredient tested positive for Cyclospora. The product was distributed in Michigan, Indiana, and California.

    Product
    Delish Vegetable Garden Salad, 10.5 oz. UPC 49022542426
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2987-2018·2018-09-12

    GE Vivid E90 Ultrasound System Recalled for Electrical Shock Risk

    GE Medical Systems is recalling Vivid E90 ultrasound systems because the power cord may break and expose electrical conductors, posing a risk of shock.

    Product
    GE Vivid E90 ultrasound system Product Usage: Vivid E80 / E90 / E95 ultrasound system is general-purpose ultrasound systems, specialized for use in cardiac imaging. It is intended for use by, or under the direction of a qualified physician for ultrasound imaging and analysis…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2984-2018·2018-09-12

    GE LOGIQ 9 Ultrasound System Recalled for Power Cord Shock Risk

    GE Medical Systems is recalling 12,426 LOGIQ 9 ultrasound systems because the power cord may break and expose electrical conductors, creating a shock hazard.

    Product
    GE LOGIQ 9 ultrasound system Product Usage: The device is intended for use by a qualified physician for ultrasound evaluation of Fetal; Abdominal; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1935-2018·2018-09-12

    Caito Foods Recalls Small Garden Salad Due to Cyclospora Contamination

    Caito Foods LLC is recalling Small Garden Salad because an ingredient tested positive for Cyclospora. The product was distributed in Michigan, Indiana, and California.

    Product
    Small Garden Salad, 9.3 oz. UPC 0081851402182
    Category
    Food
    Distribution
    3 states
  • HighFDA (Devices)·Z-2976-2018·2018-09-12

    Medline Recalls Art-Line Surgery Packs Due to Non-Sterile Component

    Medline is recalling 3,000 Art-Line Surgery Packs because a non-sterile CHG disk was attached to the outside of the sterile packaging, posing a potential infection risk.

    Product
    Art-Line Surgery Pack-LF, STERILE, 40 packs each per case.
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Devices)·Z-2986-2018·2018-09-12

    GE Vivid E80 Ultrasound System Recalled for Power Cord Shock Risk

    GE Medical Systems is recalling Vivid E80, E90, and E95 ultrasound systems because the power cord may break and expose electrical conductors, creating a shock hazard.

    Product
    GE Vivid E80 ultrasound system Vivid E80 / E90 / E95 ultrasound system is general-purpose ultrasound systems, specialized for use in cardiac imaging. It is intended for use by, or under the direction of a qualified physician for ultrasound imaging and analysis of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1951-2018·2018-09-12

    Sammy Salsa Smok'n Chipotle Recalled for Potential Cyclospora Contamination

    Sammy Food Products LLC is recalling 17 cases of Smok'n Chipotle salsa due to potential Cyclospora contamination from cilantro.

    Product
    Sammy Salsa Smok'n Chipotle, packaged in 14 oz. plastic container, 6 units per case. UPC # 00868422000134. The label is read in parts: "***INGREDIENTS: ***Fresh Tomatoes, Fresh Onions, Fresh Chile Peppers, Fresh Cilantro, Fresh Garlic, Fresh Lime, Whole Peeped Tomatoes…
    Category
    Food
    Distribution
    2 states
  • HighFDA (Devices)·Z-2983-2018·2018-09-12

    GE LOGIQ E9 Ultrasound System Recalled for Power Cord Shock Risk

    GE Medical Systems is recalling 12,426 LOGIQ E9 ultrasound systems because the power cord side may break, exposing electrical conductors and creating a risk of electric shock.

    Product
    GE LOGIQ E9 ultrasound system Product Usage: The device is intended for use by a qualified physician for ultrasound evaluation of Fetal; Abdominal; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2985-2018·2018-09-12

    GE Vivid E9 Ultrasound System Recalled for Power Cord Shock Risk

    GE Medical Systems is recalling 12,426 Vivid E9 ultrasound systems because the power cord may break and expose electrical conductors, posing a risk of electric shock.

    Product
    GE Vivid E9 ultrasound system Product Usage: GE Vivid E9 ultrasound system is a general purpose ultrasound system for use in cardiac imaging. It is intended for use by, or under direction of a qualified physician for ultrasound imaging and analysis of Fetal; Abdominal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·18220·2018-09-11

    Emerson Recalls RIDGID Wet/Dry Vacuums Due to Shock Hazard

    Emerson Tool Company is recalling RIDGID wet/dry vacuums because the on/off switch can dislodge, exposing energized wiring and posing a shock hazard.

    Product
    RIDGID® NXT HD06000 and HD09000 wet/dry vacuums
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V607000·2018-09-11

    Mercedes-Benz Recalls 2018 AMG S63 and S65 for Lane Keeping Software Defect

    Mercedes-Benz is recalling 2018 AMG S63 and S65 vehicles because the Active Lane Keeping Assist software may fail to intervene during unintended lane departures above 65 mph.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG S63, AMG S65
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18E089000·2018-09-11

    Sunright Recalls Rodia Motorcycle Helmets Due to Chin Strap Defect

    Sunright is recalling Rodia RHD200 and RHD200V motorcycle helmets because the chin strap may stretch in a crash, allowing the helmet to separate from the rider's head.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18766·2018-09-11

    John Deere Recalls Gator Utility Vehicles Due to Throttle Crash Hazard

    John Deere is recalling about 4,700 Gator utility vehicles because powertrain hardware can come loose, causing the throttle to stick and preventing the operator from stopping the vehicle.

    Product
    John Deere XUV590 and XUV590 S4 Gator™ utility vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V611000·2018-09-11

    Coach and Equipment Transit Buses Recalled for Wheelchair Lift Defect

    Coach and Equipment is recalling certain transit buses because a wheelchair lift component may fail, allowing the platform to rise too high and increasing injury risk.

    Product
    COACH AND EQUIPMENT — COACH AND EQUIPMENT PHOENIX, METRO LITE, CONDOR LT, PEGASUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V610000·2018-09-11

    Mercedes-Benz Recalls 2018 GLC Models for Incorrect Turn Signal Color

    Mercedes-Benz is recalling 2018 GLC models because the front turn signals may be pink or violet instead of the required color, potentially reducing visibility to other drivers.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 350 E, GLC 300, AMG GLC43
    Category
    Vehicle
    Distribution
    Distributed nationwide