The Recall Desk

State

Kansas product recalls

73,827 recalls have nationwide distribution and so reach Kansas. 5,822 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total
5,822
Critical
1,053
Severe
1,486
Most recent
2026-11-04

Of the 5,822 recalls naming Kansas we have scored against our rubric, 1,053 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,486 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,822 recalls whose distribution notice names Kansas specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52451–52475 of 79649

  • ModerateFDA (Devices)·Z-1942-2016·2016-06-15

    DePuy Synthes Recalls Norian Drillable Inject Due to Labeling Error

    DePuy Synthes is voluntarily recalling Norian Drillable Inject 3 CC-Sterile because the internal pouch may be labeled with the incorrect powder volume, though the actual contents are correct.

    Product
    Norian Drillable Inject 3 CC-Sterile; catalog # 07.704.003S Intended for bony voids or defects of the extremities and pelvis that are not intrinsic to the stability of the bony structure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1944-2016·2016-06-15

    Synthes Recalls Norian Drillable Inject Due to Labeling Error

    Synthes (USA) Products LLC is recalling Norian Drillable Inject 10 CC-Sterile units because the internal rotary pouch may be labeled with the incorrect powder volume, though the actual contents are correct.

    Product
    Norian Drillable Inject 10 CC-Sterile; catalog # 07.704.010S Intended for bony voids or defects of the extremities and pelvis that are not instrinsic to the stability of the bony structure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1698-2016·2016-06-15

    Ellipse ND: YAG Laser Applicator Recalled for Missing Calibration Instructions

    Ellipse A/S is recalling 25 Ellipse ND: YAG Laser applicators because they lack required instructions for calibration procedures and schedules.

    Product
    Ellipse ND: YAG Laser applicator for Ellipse Nordlys system Medical Laser Products.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1933-2016·2016-06-15

    Beckman Coulter Cholesterol Reagent Recalled for False Low Results

    Beckman Coulter is recalling Cholesterol OSR6x16 reagent because Dipyrone may cause erroneous, false low results in cholesterol assays.

    Product
    Cholesterol, Catalog No. OSR6x16 Product Usage:Cholesterol OSR6x16 is intended as a System reagent for the quantitative determination of Cholesterol concentrations in human serum on Beckman Coulter AU analyzers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1920-2016·2016-06-15

    Synthes Recalls 1.5 mm Rapid Resorbable Orbital Floor Plates Due to Labeling Errors

    Synthes (USA) Products LLC is recalling 14 units of 1.5 mm Rapid Resorbable Orbital Floor Plates because outer package expiration dates may exceed subcomponent dates.

    Product
    1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 35 mm - Sterile, Rapid Resorbable Fixation System. 1.5 mm Rapid Resorbable Orbital Floor Plate with Bending Template. Intended for use in fracture repair and reconstructive procedures of the craniofacial skeleton in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1930-2016·2016-06-15

    Beckman Coulter Lipase Reagent Recalled for Potential False Low Results

    Beckman Coulter is recalling Lipase OSR6x30 reagent because Dipyrone may cause erroneous false low results in lipase assays.

    Product
    Lipase, Catalog No. OSR6x30 Product Usage: Lipase OSR6x30 is intended as a System reagent for the quantitative determination of Lipase activity in human serum on Beckman Coulter AU analyzers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1918-2016·2016-06-15

    Synthes Recalls 22 Rapid Resorbable Orbital Floor Plates Due to Labeling Errors

    Synthes (USA) Products LLC is recalling 22 units of 1.5 mm Rapid Resorbable Orbital Floor Plates because outer package expiration dates may exceed subcomponent dates.

    Product
    1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 24 mm - Sterile, Rapid Resorbable Fixation System. 1.5 mm Rapid Resorbable Orbital Floor Plate with Bending Template. Intended for use in fracture repair and reconstructive procedures of the craniofacial skeleton in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0977-2016·2016-06-15

    Bayer Recalls Coppertone Sunscreen Lotion for Undeclared Oxybenzone

    Bayer Health Care LLC is recalling 37,512 bottles of Coppertone Sunscreen Lotion, Clearly Sheer, Broad Spectrum SPF 50, because the product contains undeclared Oxybenzone.

    Product
    Coppertone SUNSCREEN LOTION, CLEARLY SHEER, BROAD SPECTRUM SPF 50, 5 FL OZ (147mL), OTC, Dist by: Bayer HealthCare LLC, Whippany, NJ 07981 --- NDC 11523-7391-1, UPC 00041100005762
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1923-2016·2016-06-15

    Greiner Bio-One Recalls 4 ml FX Sodium Fluoride Tubes

    Greiner Bio-One is recalling 4 ml FX Sodium Fluoride/Potassium Oxalate tubes because they may contain low or no additives, potentially affecting glucose and lactate test results.

    Product
    4 ml FX Sodium Fluoride/Potassium Oxalate tube, Ref 454297 VACUETTE Glycolytic Inhibitor Tubes contain an antiglycolytic agent, sodium fluoride, and an anticoagulant, potassium oxalate. The product is suitable for the analysis of blood glucose and lactate
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1931-2016·2016-06-15

    Beckman Coulter Lactate Reagent Recalled for Potential False Low Results

    Beckman Coulter is recalling Lactate OSR6x93 reagent because Dipyrone may cause erroneous false low results.

    Product
    Lactate, Catalog No. OSR6x93 Product Usage: Lactate OSR6x93 is intended as a System reagent for the quantitative determination of L-Lactate in human plasma and cerebrospinal fluid (CSF) on Beckman Coulter AU analyzers.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1696-2016·2016-06-15

    Philips DuraDiagnost X-ray System Recalled for Image Acquisition Failure

    Philips Healthcare is recalling five DuraDiagnost stationary X-ray systems because the detector may incorrectly signal readiness, causing failed image acquisitions.

    Product
    Philips Healthcare DuraDiagnost stationary X-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V433000·2016-06-14

    PJ Trailers Recalls T1 Trailers Due to Tongue Strength Defect

    PJ Trailers is recalling 2015-2016 T1 single axle tilt trailers because a notch in the steel tongue may compromise its strength, increasing crash risk.

    Product
    PJ TRAILERS — PJ TRAILERS T1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V432000·2016-06-14

    KZRV Recalls 2016-2017 Spree Travel Trailers Due to Fire Risk

    KZRV is recalling 2016-2017 Spree travel trailers because incorrectly installed refrigerator vents may cause overheating and increase the risk of fire.

    Product
    KZRV — KZRV SPREE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V434000·2016-06-14

    Micro Bird Recalls 2015-2016 Transit Buses for Window Shattering Risk

    Micro Bird is recalling 79 model year 2015-2016 transit buses because water accumulation in window frames can cause glass to shatter in freezing conditions.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS, CT-SERIES, MB II TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E057000·2016-06-13

    Triumph Recalls Aftermarket Brake Levers for 2016-2017 Motorcycles

    Triumph is recalling aftermarket adjustable brake levers for specific 2016-2017 motorcycles because they may contact the handlebar, preventing maximum braking force.

    Product
    TRIUMPH — TRIUMPH BONNEVILLE T100 BLACK A3, STREET TWIN, THRUXTON, BONNEVILLE T100 BLACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V427000·2016-06-13

    Vermeer Recalls 2014-2016 TG5000 Trailers Due to Brake Defect

    Vermeer is recalling 2014-2016 TG5000 trailers because incorrect pushrod lengths may cause parking brakes to engage unintentionally, increasing crash risk.

    Product
    VERMEER — VERMEER TG5000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V430000·2016-06-13

    Nissan Recalls Infiniti Q50 Models for Steering System Error

    Nissan is recalling 2014-2016 Infiniti Q50 and Q50 Hybrid vehicles because a steering system error may alter responsiveness and increase crash risk.

    Product
    INFINITI — INFINITI Q50, Q50 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16E056000·2016-06-13

    Wilson Manifolds Recalls Peter Paul Nitrous Solenoid Valves

    Wilson Manifolds is recalling specific Peter Paul 22X01031GM 12/DC solenoid valves due to improper welding that may cause the piston to eject under pressure.

    Product
    FUEL SYSTEM, OTHER:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide