The Recall Desk

State

Kansas product recalls

73,817 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.

These figures cover only the 5,822 recalls whose distribution notice names Kansas specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46576–46600 of 79639

  • SevereUSDA FSIS·067-2017·2017-06-09

    Tyson Recalls Breaded Chicken Products Due to Undeclared Milk Allergen

    Tyson Foods is recalling approximately 2.5 million pounds of ready-to-eat breaded chicken products because they may contain undeclared milk, a known allergen.

    Product
    Tyson Foods, Inc. — Tyson Foods Inc. Recalls Ready-To-Eat Breaded Chicken Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·068-2017·2017-06-09

    Gourmet Boutique Recalls Breaded Chicken Products Due to Undeclared Milk Allergen

    Gourmet Boutique LLC is recalling approximately 294,744 pounds of ready-to-eat breaded chicken products because they may contain undeclared milk, a known allergen.

    Product
    Gourmet Boutique, LLC — Gourmet Boutique LLC Recalls Ready-To-Eat Breaded Chicken Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V371000·2017-06-09

    Chrysler Recalls 2017 Pacifica Plug-In Hybrids for Inverter Defect

    Chrysler is recalling 2017 Pacifica Plug-In Hybrids because a power inverter defect may cause the vehicle to stop moving, increasing crash risk.

    Product
    CHRYSLER — CHRYSLER PACIFICA PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·061-2017·2017-06-08

    Maid-Rite Recalls Beef Products Due to Undeclared Milk Allergen

    Maid-Rite Specialty Foods is recalling approximately 174,000 pounds of beef products because they contain undeclared milk, a known allergen.

    Product
    Maid-Rite Specialty Foods, Inc — Maid-Rite Specialty Foods, LLC. Recalls Beef Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·17V369000·2017-06-08

    Supreme Signature Van and Kold King Recall for Rear Reflector Height

    Supreme is recalling 2007-2017 Signature Van and Kold King vehicles because rear reflex reflectors may be mounted too high, failing federal safety standards and increasing crash risk.

    Product
    SUPREME — SUPREME SIGNATURE VAN, KOLD KING
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17175·2017-06-08

    GT Mountain Bicycles Recalled Due to Handlebar Crack Hazard

    Cycling Sports Group is recalling about 1,000 GT mountain bicycles because the handlebars can crack, posing a fall hazard to consumers.

    Product
    GT mountain bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V368000·2017-06-07

    Porsche Recalls Panamera and Cayenne Models for Engine Stall Risk

    Porsche is recalling specific 2010-2012 Panamera and 2011 Cayenne vehicles because loose camshaft controllers may cause the engine to stall, increasing crash risk.

    Product
    PORSCHE — PORSCHE PANAMERA S, PANAMERA 4S, PANAMERA TURBO, PANAMERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0877-2017·2017-06-07

    SCA Pharmaceuticals Recalls Cefazolin Sodium Bags Due to Leaking

    SCA Pharmaceuticals is recalling 70 bags of cefazolin sodium due to leaks at the seam, which compromises the product's sterility.

    Product
    ceFAZolin sodium added to 100 mL 0.9% Sodium Chloride injectable, 3g, Total Approximate Volume 115 mL, Single Dose Container bag, Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0524-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0879-2017·2017-06-07

    SCA Pharmaceuticals Recalls Phenylephrine Injectable Bags Due to Leaking

    SCA Pharmaceuticals is recalling 30 bags of Phenylephrine HCL injectable solution because the bags are leaking at the seam, compromising sterility.

    Product
    PHENYLephrine HCL in 0.9% Sodium Chloride injectable, 10 mg (Final Concentration = 0.1 mg per mL) Total Volume 100 mL, Single Dose Container bag, Preservative Free (Contains Sulfites), Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC: 70004-0810-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0871-2017·2017-06-07

    SCA Pharmaceuticals Recalls Morphine Sulfate Injectable Bags Due to Leaking

    SCA Pharmaceuticals is recalling 56 bags of morphine sulfate in 0.9% Sodium Chloride injectable because the bags are leaking at the seam, compromising sterility.

    Product
    morphine sulfate in 0.9% Sodium Chloride injectable, 1 mg per mL, Total Volume 100 mL, Single Dose Container bag, (Total morphine Dose 100 mg/ 100 mL), Preservative Free (Contains Sulfites), Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205, NDC 70004-0100-55
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0870-2017·2017-06-07

    SCA Pharmaceuticals Recalls Morphine Sulfate Injectable Bags Due to Leaking

    SCA Pharmaceuticals is recalling 80 bags of morphine sulfate injectable solution because the bags are leaking at the seam, compromising sterility.

    Product
    morphine sulfate in 0.9% Sodium Chloride injectable, 1 mg per mL, Total Volume 100 mL, Single Dose Container bag, (Total morphine Dose 100 mg/ 100mL), Preservative Free (Contains Sulfites), Rx only, SCA Pharmaceuticals, 8821 Knoedl Ct, Little Rock, AR 72205, NDC 70004-0100-32.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0874-2017·2017-06-07

    SCA Pharmaceuticals Recalls Fentanyl Injectable Bags Due to Sterility Concerns

    SCA Pharmaceuticals is recalling fentanyl citrate injectable bags because they are leaking at the seam, which compromises sterility.

    Product
    fentaNYL (as citrate) in 100mL 0.9% Sodium Chloride injectable,20 mcg per mL, Single Dose Container bag, (Total fentanyl Dose 2,000 mcg/100 mL) Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-203-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0878-2017·2017-06-07

    SCA Pharmaceuticals Recalls Leaking Magnesium Sulfate Injectable Bags

    SCA Pharmaceuticals is recalling 40 bags of Magnesium Sulfate injectable solution due to seam leaks that compromise sterility.

    Product
    MAGNESIUM Sulfate added to 100 mL 0.9% Sodium Chloride injectable, 4g, Total Approximate Volume 108 mL (does not include mfg. overfill) Single Dose Container bag, Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC: 70004-0737-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0875-2017·2017-06-07

    SCA Pharmaceuticals Recalls Hydrocodone Injectable Bags Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 87 bags of Hydromorphone HCL injectable solution because the bags are leaking at the seam, compromising sterility.

    Product
    HYDROmorphone HCL in 0.9% Sodium Chloride injectable, 0.2 mg per ml, Total Volume 100mL, Single Dose Container bag, (Total HYDROmorphone Dose 20 mg per 100 mL) Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0300-55
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0876-2017·2017-06-07

    SCA Pharmaceuticals Recalls Leaking Cefazolin Sodium Injectable Bags

    SCA Pharmaceuticals is recalling 240 bags of cefazolin sodium injectable due to seam leaks that compromise sterility.

    Product
    ceFAZolin sodium added to 100 mL 0.9% Sodium Chloride injectable, 2g, Total Approximate Volume 100 mL, Single Dose Container bag, Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0522-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0872-2017·2017-06-07

    SCA Pharmaceuticals Recalls Fentanyl Injection Bags Due to Seam Leaks

    SCA Pharmaceuticals is recalling 118 bags of fentanyl injection due to seam leaks that compromise sterility. The product was distributed nationwide in the USA.

    Product
    fentaNYL (as citrate) in 0.9% Sodium Chloride injectable,10 mcg per mL, Total Volume 100 mL, Single Dose Container bag, (Total fentanyl Dose 1,000 mcg/100 mL) Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0229-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0873-2017·2017-06-07

    SCA Pharmaceuticals Recalls Fentanyl Injection Bags Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 370 bags of fentanyl injection solution because the bags were leaking at the seam, compromising sterility.

    Product
    fentaNYL (as citrate) in 0.9% Sodium Chloride injectable,10 mcg per mL, Total Volume 100 mL, Single Dose Container bag, (Total fentanyl Dose 1,000 mcg/100 mL) Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0202-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2283-2017·2017-06-07

    Trident Battered Cod Recalled Due to Potential Plastic Contamination

    Trident Seafoods is recalling frozen Battered Cod Diamonds because they may contain small pieces of plastic.

    Product
    Trident Item # 474568, Irregulars Battered Cod 3 oz Battered Diamonds, food service packages, frozen, Net wt. 10 lbs.
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-2179-2017·2017-06-07

    GE Healthcare Recalls Patient Steps on RFX, Legacy, and Precision 500D Systems

    GE Healthcare is recalling 2,380 patient steps for RFX, Legacy, and Precision 500D systems because they may detach from the table, posing a fall risk.

    Product
    Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2176-2017·2017-06-07

    AbbVie Recalls 673 PEG Kits Due to Sterility Concerns

    AbbVie Inc. is voluntarily recalling 673 PEG kits because they may not be sterile. The recall covers lots distributed nationwide and internationally.

    Product
    AbbVie PEG, PEG Kit 20FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2217-2017·2017-06-07

    Cardinal Digital Bariatric Scales Recalled Due to Seat Failure Risk

    Cardinal Scale Mfg Co is recalling 975 digital bariatric scales because a seat may fail unexpectedly, posing an injury risk.

    Product
    Cardinal, Digital Bariatric Scale 1) model 6876, Cap 600 and 2) model 6868 Cap 1000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2277-2017·2017-06-07

    Trident Multi-Grain Alaskan Cod Recalled for Plastic Contamination

    Trident Seafoods is recalling 12 oz. packages of Multi-Grain Alaskan Cod because they may contain small pieces of plastic.

    Product
    Trident Item # 421048, Multi-Grain Alaskan Cod, Frozen, RETAIL packages, Net wt. 12 oz. UPC 0 28029 21048 4 The retail label is read in parts: "***Trident SEAFOODS***Multi-Grain Alaskan Cod***NET WT. 12 OZ.***". The retail case label is read in parts: "***Trident…
    Category
    Food
    Distribution
    26 states