The Recall Desk

State

Kansas product recalls

72,940 recalls have nationwide distribution and so reach Kansas. 5,723 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total
5,723
Critical
1,045
Severe
1,228
Most recent
2026-09-02

Of the 5,723 recalls naming Kansas we have scored against our rubric, 1,045 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,228 (21%) are Severe.

Which agencies issued them

These figures cover only the 5,723 recalls whose distribution notice names Kansas specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3701–3725 of 78663

  • HighFDA (Devices)·Z-1042-2026·2026-01-21

    Angioplasty balloon catheters recalled over inflation and deflation difficulty

    Boston Scientific is recalling 21 Coyote over-the-wire PTA balloon dilatation catheters over the potential for inflation and deflation difficulty during use in the peripheral vasculature.

    Product
    Boston Scientific Coyote OVER-THE-WIRE PTA Balloon Dilation Catheter, 4F, 1) 2.5mm x120mm, 150 cm, UPM/Model No. REF H74939186251210; 2) 3.5mm x120mm, 150 cm, UPM/Model No. REF H74939186351210; Catheter, Angioplasty, Peripheral, Transluminal
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1093-2026·2026-01-21

    Cell wash solution recalled over fungal contamination of an affected lot

    Hologic is recalling 3,728 units of ThinPrep CytoLyt Solution over fungal contamination of the affected lot with Parengyodontium album.

    Product
    ThinPrep¿ CytoLyt¿ Solution. Buffered Cell Wash Solution.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0282-2026·2026-01-21

    Carmex lip balm recalled over insanitary conditions at a distribution center

    Gold Star Distribution is recalling Carmex over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.

    Product
    Carmex a) jar, 12 count, UPC: 083078123154, 083078113155; b) Tube, PEG, 12 count, UPC: 083078123147, 083078113148
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1092-2026·2026-01-21

    Patient positioning systems recalled over stereotactic radiosurgery tolerance errors

    C-RAD Positioning is recalling 189 Catalyst and Catalyst+ systems because the system may indicate a patient as correctly positioned at the isocenter when it is outside tolerance.

    Product
    Brand Name: Catalyst+ Product Name: Catalyst, Catalyst+ Model/Catalog Number: SP001-0026, SP003-0002 Software Version: cSRS module in combination with cMotion module Product Description: GMDN: 40893 Patient positioning device, diagnostic imaging/radiotherapy, laser Component
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0401-2026·2026-01-21

    SMV BodyTrack nuclear medicine systems recalled over a potential detector fall

    GE HealthCare is recalling 12 units of the SMV BodyTrack nuclear medicine system, because systems moved without adequate detector support may suffer a detector fall.

    Product
    Jumbo RAW SHRIMP, All Natural, Chemical Free, No artificial ingredients, NET WT. 32 OZ (2 LB) 907g UPC: 1 93968 00697 6
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0287-2026·2026-01-21

    Ground cinnamon recalled over elevated levels of lead

    Eureka Inc is recalling 32 cases of ground cinnamon in 100g clear plastic containers over elevated levels of lead.

    Product
    Toothpaste: a) COLGATE, TOOTHPASTE, WHITENING, 2.5oz, 24ct; UPC: 035000511065; b) COLGATE, TOOTHPASTE, Regular, 2.5oz, 24ct, UPC: 035000511058; c) COLGATE, TOOTHPASTE, TRIPLE, 2.5oz, 24ct, UPC: 035000512109; d) COLGATE, TOOTHPASTE, MINT ZING, 24CT, 2.5oz, UPC: 035000744609; COLGA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0283-2026·2026-01-21

    Shrimp paste recalled after the product tested high for lead

    Gusto Group is recalling 7 cases of Klong Kone shrimp paste after the product tested high for lead.

    Product
    Personal Care, Vaporizing Chest Rub, 4 oz, 12 count, UPC 048155903319
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0285-2026·2026-01-21

    Petroleum jelly recalled over insanitary conditions at a distribution center

    Gold Star Distribution is recalling Petroleum jelly over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.

    Product
    Petroleum jelly: a) Vaseline Petroleum Jelly, 1.75, 12CT, UPC: 6001085120946; b) Vaseline Men Cooling Petroleum Jelly, 100ML, 12CT, UPC: 60022141; c) Vaseline Vitamin E, Petroleum Jelly, 100ML, 12CT, UPC: 6001085121028; MEN FRESH PETROLEUM JELLY, 100ML, 12CT, UPC: 60022127; d) Lu
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1079-2026·2026-01-21

    Azurion interventional systems recalled over nine identified software issues

    Philips Medical Systems Nederland is recalling 990 Azurion R3.0 systems over nine identified software issues, including loss of X-ray after a pedal tap and continuous restart.

    Product
    Philips Azurion Systems R3.0. Includes the following label descriptions and corresponding models: 1. Azurion 3 M12. Model Number: 722229. 2. Azurion 3 M15. Model Number: 722230. 3. Azurion 5 M12. Model Number: 722231. 4. Azurion 5 M20. Model Number: 722232. 5.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0398-2026·2026-01-21

    Non-dairy frozen dessert recalled over foreign material in millions of units

    WhiteWave is recalling 4,665,608 US units of So Delicious Dairy Free Salted Caramel Cluster Cashewmilk non-dairy frozen dessert over foreign material.

    Product
    So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, Non-Dairy Frozen Dessert, One Pint (473 mL). UPC 744473 476138. Manufactured By/For So Delicious Dairy Free Eugene, OR 97402 So Delicious Dairy Free Salted Caramel Cluster Cashewmilk, Non-Dairy Frozen Dessert. Net wt. 50
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0262-2026·2026-01-21

    Aleve recalled over insanitary conditions at a distribution center

    Gold Star Distribution is recalling Aleve over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.

    Product
    Aleve 1's, 60 CT
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0263-2026·2026-01-21

    Alka Seltzer recalled over insanitary conditions at a distribution center

    Gold Star Distribution is recalling Alka Seltzer over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.

    Product
    Alka Seltzer, a) Original, 2 tablets per packet in 58 count box, UPC: 815556020033, 016500514473, b) Plus Cold & Flu, 2 tablets per packet in 36 count box, UPC: 016500594932
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1094-2026·2026-01-21

    Infusion pumps recalled over speakers that may not produce audible alarms

    ICU Medical is recalling 423 Plum Duo Infusion Systems after one lot of defective primary speakers may fail to produce sound, so the pump may not produce audible alarms or alerts.

    Product
    Plum Duo Infusion System, List Number 40002-04-01
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0272-2026·2026-01-21

    Liquid NyQuil recalled over insanitary conditions at a distribution center

    Gold Star Distribution is recalling Liquid NyQuil over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.

    Product
    LIQUID NYQUIL a) regular, 12/8oz; b) cherry, 12/8oz
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0277-2026·2026-01-21

    Tylenol products recalled over insanitary conditions at a distribution center

    Gold Star Distribution is recalling Tylenol over CGMP deviations, citing insanitary conditions including rodent exposure and activity at its distribution center.

    Product
    TYLENOL a) 500 MG., 2'S DISPLAY, 50CT; b) COLD & FLU, 25CT/2S; c) COLD & FLU SEVERE, 2PK, 50CT; d) PM, 50CT; e) SINUS SEVERE, 2PK, 50CT
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1062-2026·2026-01-21

    Allura Xper FD10C systems recalled over a missing cooling unit drip tray

    Philips Medical Systems Nederland is recalling 38 Allura Xper FD10C systems because the drip tray beneath the cooling unit may not have been installed.

    Product
    Product Name: Allura Xper FD10C; Model number: 722001;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1051-2026·2026-01-21

    Pre-op kits recalled because they contain recalled B. Braun administration sets

    Medline is recalling 32 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: 1) DELUXE PRE OP KIT, Medline SKU DYKS2034A; 2) DELUXE PRE OP KIT, Medline SKU DYKS2006B.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1087-2026·2026-01-21

    PALACOS MV bone cement recalled because ampoules may not break

    Heraeus Medical is recalling PALACOS MV pro 40 and PALACOS MV pro 80 bone cement because an unfortunate combination of factors can leave ampoules unbroken, so no appropriate cement dough is formed.

    Product
    Medline medical procedure convenience kits labeled as: 1) WCH BARI-GASTRECTOMY CDS, REF CDS860237AF; 2) ROBOTIC PROCEDURE, REF CDS982128Q; 3) CUH THORACIC, REF CDS984338M; 4) THORACIC PROCEDURE, REF CDS984640I; 5) DAVINCI ROBOTIC PACK-LF, REF DYNJ0525321O; 6) LAP CHO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1077-2026·2026-01-21

    Allura Xper FD20/20 systems recalled over a missing cooling unit drip tray

    Philips Medical Systems Nederland is recalling 8 units of the Allura Xper FD20/20, model 722038, because the drip tray beneath the cooling unit may not have been installed.

    Product
    Allura Xper FD20/20; Model Number: 722038;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1059-2026·2026-01-21

    Neuro angio packs recalled over recalled B. Braun administration sets inside

    Medline is recalling 12 units of kits containing B. Braun IV administration sets, which were recalled because check valve components may become stuck in the open or closed positions.

    Product
    Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as: NEURO ANGIO PACK, Medline kit SKU DYNJ38935
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1043-2026·2026-01-21

    Neurostimulator clinician programmer app recalled over faults during device use

    Medtronic is recalling 7,123 units of the Vanta Clinician Programmer Application after complaints that it does not function as intended during use.

    Product
    A71200 Vanta" Clinician Programmer Application (CP App) version 2.0.2465 and 2.0.2683, Product number A71200. Software is deployed and operated on Samsung tablets (CFN CT900).
    Category
    Medical Device
    Distribution
    Distributed nationwide