The Recall Desk

State

Kansas product recalls

73,738 recalls have nationwide distribution and so reach Kansas. 5,821 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total
5,821
Critical
1,053
Severe
1,485
Most recent
2026-10-28

Of the 5,821 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 1,485 (26%) are Severe.

These figures cover only the 5,821 recalls whose distribution notice names Kansas specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

34801–34825 of 79559

  • HighFDA (Devices)·Z-2382-2019·2019-09-04

    Bard Equistream Hemodialysis Catheter Recalled for Tip Damage

    Bard Peripheral Vascular Inc is recalling Equistream XK hemodialysis catheters because the molded tip may break or become damaged during placement.

    Product
    EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5913420, 16F, Straight, 42cm length, BARD, UDI: 00801741013881
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Food)·F-2108-2019·2019-09-04

    PreGel Lemon 50 Recalled for Undeclared Milk Allergen

    PreGel America, Inc. is recalling PreGel Lemon 50 because a complaint indicated the presence of undeclared milk, which is not listed on the ingredient statement.

    Product
    PreGel Lemon 50 4.4 lb (2kg) bag, Ingredients: dextrose, citric acid, mono and diglycerides of fatty acids, propane -1,2-diol esters of fatty acids, maltodextrins, carboxymethylcellulose, guar gum, flavors, dehydrated lemon juice, xanthan gum Manufactured by: PreGel America…
    Category
    Food
    Distribution
    28 states
  • HighFDA (Devices)·Z-2383-2019·2019-09-04

    Bard GlidePath Hemodialysis Catheter Recalled for Tip Breakage

    Bard Peripheral Vascular Inc is recalling GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.

    Product
    GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5393190, 14.5F, Straight, 19cm length, BARD, UDI: 00801741012174
    Category
    Medical Device
    Distribution
    53 states
  • HighCPSC·19776·2019-09-04

    John Deere Recalls XUV835 Gator Utility Vehicles Due to Throttle Hazard

    John Deere is recalling about 19,730 XUV835 Gator utility vehicles because the throttle cable sheathing can melt, causing the throttle to stick and posing a crash hazard.

    Product
    John Deere XUV835 Gator utility vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2399-2019·2019-09-04

    Siemens SOMATOM go.Now CT Systems Recalled for Injector Holder Risk

    Siemens is recalling SOMATOM go.Now CT systems because the injector holder could fall off with the injector and storage box.

    Product
    SOMATOM go.Now; Models #11061610 & 11061618 Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2371-2019·2019-09-04

    Bard Hemodialysis Catheter Recalled Due to Tip Breakage During Placement

    Bard Peripheral Vascular Inc is recalling 1,356 EQUISTREAM Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during the placement procedure.

    Product
    EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet, REF/Product code:5903190, 14.5F, Straight ,19cm length, BARD, UDI# 00801741013690
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-2389-2019·2019-09-04

    Bard GlidePath Hemodialysis Catheter Recalled for Tip Breakage

    Bard Peripheral Vascular Inc is recalling 104 units of GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.

    Product
    GlidePath Long-Term Hemodialysis Catheter, REF/Product code:5396280, 14.5F, Alphacurve, 28cm length, BARD, UDI: 00801741012266
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-2375-2019·2019-09-04

    Bard Equistream Hemodialysis Catheter Recalled for Molded Tip Defects

    Bard Peripheral Vascular Inc is recalling 39 units of Equistream Long-Term Hemodialysis Catheters because the molded tip may break or become damaged during placement.

    Product
    EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet, REF/Product code:5904270, 14.5F, Straight ,27cm length, BARD, UDI: 00801741013775
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-2404-2019·2019-09-04

    Siemens SOMATOM go.Top CT Scanner Recall for Falling Injector Holder

    Siemens is recalling 12 SOMATOM go.Top CT scanners because the injector holder could fall off. The devices are distributed in 20 US states.

    Product
    SOMATOM go.Top; Models #11061640 Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2422-2019·2019-09-04

    Stryker Endotrac EPF/EGR Triangle Blade Recall for Compromised Sterile Seal

    Stryker GmbH is recalling 21 Endotrac EPF/EGR Triangle Blades because the sterile bag seal integrity may be compromised, posing a risk of contamination.

    Product
    Endotrac EPF/EGR Triangle Blade, Angled, Catalog Number 3054A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2373-2019·2019-09-04

    Bard Equistream Hemodialysis Catheter Recall Due to Tip Breakage

    Bard Peripheral Vascular Inc is recalling 161 units of Equistream Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.

    Product
    EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet, REF/Product code:5903270, 14.5F, Straight ,27cm length, BARD, UDI: 00801741013713
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-2413-2019·2019-09-04

    Stryker Endotrac ECTR Push Blade Recalled for Sterile Bag Seal Integrity

    Stryker GmbH is recalling 476 Endotrac ECTR Push Blades because the sterile bag seal integrity may be compromised, potentially affecting sterility.

    Product
    Endotrac ECTR Push Blade, Catalog Number 2053-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2370-2019·2019-09-04

    Bard Equistream Hemodialysis Catheter Recalled for Tip Damage

    Bard Peripheral Vascular Inc is recalling 40 units of Equistream Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.

    Product
    EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product code:5905280, 14.5 Fr. Alphacurve Catheter with Standard Kit, 28cm length, BARD, UDI# 00801741013812
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-2364-2019·2019-09-04

    CooperSurgical Recalls TransWarmer Infant Mattresses Due to Burn Risk

    CooperSurgical is recalling TransWarmer Warming Infant Transport Mattresses because some units lack updated instructions prohibiting use with other heat devices, which could cause skin burns.

    Product
    TransWarmer Warming Infant Transport Mattress, Model no. 20421 Product Usage: The TransWarmer¿ Warming Infant Transport Mattress is gel-filled, disposable mattress that provides heat for up to two hours when cold stress is a concern. The patented WarmGel heats up to 104…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2388-2019·2019-09-04

    Bard GlidePath Hemodialysis Catheter Recalled for Tip Breakage

    Bard Peripheral Vascular Inc is recalling 570 units of GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or become damaged during placement.

    Product
    GlidePath Long-Term Hemodialysis Catheter, REF/Product code:5396240, 14.5F, Alphacurve, 19cm length, BARD, UDI: 00801741012259
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-2402-2019·2019-09-04

    Siemens SOMATOM go.All CT Scanner Recall for Falling Injector Holder

    Siemens is recalling 10 SOMATOM go.All CT scanners because the injector holder could fall off. The units are distributed in 20 US states.

    Product
    SOMATOM go.All; Models #11061630 Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·19778·2019-09-04

    John Deere Recalls Frontier Grooming Mowers Due to Entanglement Hazard

    John Deere is recalling Frontier grooming mowers because incorrect driveline assembly can prevent the safety shield from spinning, posing an entanglement injury risk.

    Product
    Frontier FM3012, GM1060, GM1072, GM1084, GM1190, GM3060, and GM3072 grooming mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2393-2019·2019-09-04

    Bard GlidePath Hemodialysis Catheter Recalled for Tip Breakage

    Bard Peripheral Vascular Inc is recalling 91 units of GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.

    Product
    GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet, REF/Product code:5397310, 14.5F, straight, 31cm length, BARD, UDI: 00801741012327
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-2384-2019·2019-09-04

    Bard Hemodialysis Catheter Recalled for Molded Tip Breakage During Placement

    Bard Peripheral Vascular Inc is recalling GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during the placement procedure.

    Product
    GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5393230, 14.5F, Straight, 23cm length, BARD, UDI: 00801741012181
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-2394-2019·2019-09-04

    Bard GlidePath Hemodialysis Catheter Recalled for Tip Breakage

    Bard Peripheral Vascular Inc is recalling 39 units of GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.

    Product
    GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet, REF/Product code:5397350, 14.5F, straight, 35cm length, BARD, UDI: 00801741012334
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-2381-2019·2019-09-04

    Bard Equistream XK Hemodialysis Catheter Recalled for Tip Defect

    Bard Peripheral Vascular Inc is recalling 2 units of Equistream XK hemodialysis catheters because the molded tip may break or be damaged during placement.

    Product
    EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5913310, 16F, Straight, 31cm length, BARD, UDI: 00801741013867
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-2391-2019·2019-09-04

    Bard GlidePath Hemodialysis Catheter Recalled for Tip Breakage

    Bard Peripheral Vascular Inc is recalling GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.

    Product
    GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet, REF/Product code:5397230, 14.5F, straight, 23cm length, BARD, UDI: 00801741012303
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-2376-2019·2019-09-04

    Bard Equistream XK Hemodialysis Catheter Recalled for Tip Breakage

    Bard Peripheral Vascular Inc is recalling Equistream XK Alphacurve Long-Term Hemodialysis Catheters because the molded tip may break or become damaged during placement.

    Product
    EQUISTREAM XK Alphacurve Long-Term Hemodialysis Catheter REF/Product code:5915240, 16F, 24cm length, BARD, UDI: 00801741013904
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-2369-2019·2019-09-04

    Bard Equistream Hemodialysis Catheter Recalled for Tip Breakage

    Bard Peripheral Vascular Inc is recalling 135 units of Equistream Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.

    Product
    EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product code:5905240, 14.5 Fr. Alphacurve Catheter with Standard Kit, 24cm length, BARD, UDI# 00801741013805
    Category
    Medical Device
    Distribution
    53 states
  • HighFDA (Devices)·Z-2400-2019·2019-09-04

    Siemens SOMATOM go.Up CT Systems Recalled for Falling Injector Holder

    Siemens is recalling 18 SOMATOM go.Up CT systems because the injector holder could fall off, posing a risk of injury.

    Product
    SOMATOM go.Up; Models #11061620 Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data
    Category
    Medical Device
    Distribution
    Distributed nationwide