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.

Which agencies issued them

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.

44751–44775 of 79639

HighFDA (Devices)·Z-3059-2017·2017-08-30
Custom Assemblies Recalls Custom Surgical Kits with Defective BD Needles
Custom Assemblies Inc is recalling 2,155 custom surgical kits because they contain BD SafetyGlide needles with loose polypropylene particulate in the fluid path.
Product
Various custom surgical kits manufactured for CMS, CUSTOM MEDICAL SPECIALTIES, INC.: (a) CMS-4153-R2 MPM Biopsy TRAY (b) CMS-5832-R1 Custom Safety Mammo Biopsy Tray (c) CMS-4108 Multipurpose Safety Tray (d) CMS-3141-R6 Custom Ultrasound Tray (e) CMS-2891-R1 Custom Safety…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·17V538000·2017-08-30
REV Recalls 2018 Fleetwood and Holiday Rambler Motorhomes for Wiring Defect
REV is recalling 2018 Fleetwood Jamboree and Holiday Rambler Vesta motorhomes because improperly stripped generator wires may cause an electrical short and fire.
Product
FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER JAMBOREE, VESTA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3066-2017·2017-08-30
Shippert Medical Technologies Recalls Tissu-Trans SFILL 360 Due to Seal Integrity
Shippert Medical Technologies is recalling Tissu-Trans SFILL 360 devices because the seal integrity of the sterile packages cannot be assured.
Product
Tissu-Trans SFILL 360, 3-TT-SFILL 360. Product Usage: Intended for fat transfer and liposuction.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3049-2017·2017-08-30
Alcon ORA System Recall for Incorrect IOL Power Measurements
Alcon is recalling 429 ORA Systems with VerifEye+ Carts due to a software error that may cause incorrect intraocular lens power measurements during cataract surgery.
Product
ORA System with VerifEye+ Cart, Catalog Number 8065998307 For use during intraocular lens surgery
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3061-2017·2017-08-30
Shippert Medical Technologies Recalls Tissu-Trans Filtron 250 Due to Seal Integrity
Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 250 because the seal integrity of the sterile packages cannot be assured.
Product
Tissu-Trans Filtron 250, 3-TT-FILTRON 250. Product Usage: Intended for fat transfer and liposuction.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3052-2017·2017-08-30
Medtronic Curved Suction 70 Recalled for Verification Failure
Medtronic is recalling 149 Curved Suction 70 ENT instruments because they fail required pre-use verification checks.
Product
Medtronic Curved Suction 70 9733450 EM ENT, reusable, Rx. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. The suction devices are part of a family of reusable ENT instruments that are used with the StealthStationTM AxiEM surgical navigation system.…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3063-2017·2017-08-30
Shippert Medical Technologies Recalls Tissu-Trans Filtron 1000 Due to Seal Integrity
Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 1000 because the seal integrity of the sterile packages cannot be assured.
Product
Tissu-Trans Filtron 1000, 3-TT-FILTRON 1000. Product Usage: Intended for fat transfer and liposuction.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3064-2017·2017-08-30
FDA Recalls Tissu-Trans Filtron 2000 Due to Sterile Seal Integrity Concerns
Shippert Medical Technologies is recalling 5,188 units of Tissu-Trans Filtron 2000 because the sterile package seal integrity cannot be assured.
Product
Tissu-Trans Filtron 2000, 3-TT-FILTRON 2000. Product Usage: Intended for fat transfer and liposuction.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3065-2017·2017-08-30
Shippert Medical Technologies Recalls Tissu-Trans MEGA 1500 Due to Seal Integrity
Shippert Medical Technologies is recalling Tissu-Trans MEGA 1500 devices because the seal integrity of the sterile packages cannot be assured.
Product
Tissu-Trans MEGA 1500, 3-TT-MEGA 1500. Product Usage: Intended for fat transfer and liposuction.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3058-2017·2017-08-30
Medtronic ENT Navigation Suction Devices Recalled for Verification Failure
Medtronic Navigation is recalling six kits of ENT suction devices because they fail required pre-use verification checks.
Product
Medtronic ENT Prgm 9734636 Add Fusion Nav AxiEM, reusable, Rx. This kit includes 9733908 (which includes 9733452 containing 9733449, Straight Suction, 9733450, 70 deg Curved Suction, and 9733451, 90 deg Curved Suction). The firm name on the label is Medtronic Navigation, Inc.…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·17V539000·2017-08-30
New Flyer Transit Bus Seat Belt Buckle Recall
New Flyer is recalling 2015-2017 transit buses because the driver's seat belt buckle may be stuck, preventing the belt from latching.
Product
NEW FLYER — NEW FLYER MD30, XD40, XN40, MD35
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-3400-2017·2017-08-30
Shatto Milk Ice Cream Sandwiches Recalled for Undeclared Allergens
Shatto Milk Company is recalling 140 bags of ice cream sandwiches due to undeclared milk and wheat allergens.
Product
Sugary, Sugar Cookie And Strawberry Ice Cream Sammich, packaged in 4 oz plastic bags. Shatto Milk Company, Osborn, MO.
Category
Food
Distribution
1 state
HighFDA (Food)·F-3397-2017·2017-08-30
Shatto Milk Co Recalls Buzzzz Honey Butter for Undeclared Milk Allergen
Shatto Milk Co is recalling Buzzzz Honey Butter because the product fails to disclose the presence of milk, a major food allergen.
Product
Buzzzz Honey Butter, packaged in 8 oz plastic tubs. Plant # 29-685 Osborn, MO.
Category
Food
Distribution
1 state
HighFDA (Food)·F-3395-2017·2017-08-30
Shatto Milk Co Recalls Plain Ol' Butter for Undeclared Milk Allergen
Shatto Milk Co is recalling Plain Ol' Butter because the packaging fails to disclose the presence of milk, a major allergen.
Product
Plain Ol' Butter, packaged in 8 oz plastic tubs. Plant # 29-685 Osborn, MO.
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-3069-2017·2017-08-30
Medtronic Recalls Deep Brain Stimulation Lead Kits Due to Depth Stop Defect
Medtronic is recalling Deep Brain Stimulation lead kits because the depth stop may not secure properly, potentially causing the lead to be placed beyond the intended target.
Product
DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation (DBS) lead kits, models 3387/3387S, 3389/3389S, and 3391/3391S, The lead kit contains one DBS lead in addition to multiple accessories used in DBS lead implant procedures. Among these accessories is the DBS lead…
Category
Medical Device
Distribution
47 states
HighFDA (Food)·F-3409-2017·2017-08-30
Grandma's Herbs Cholesterol Support Recalled for Undeclared Soy Lecithin
Grandma's Herbs is recalling Cholesterol Support dietary supplements because they contain undeclared soy lecithin, a common allergen.
Product
"Because They Work" GRANDMA'S HERBS CHOLESTEROL SUPPORT, Dietary Supplement, 100 Capsules 480 mg. Packaging: PET plastic bottles, UPC# 714938 00046
Category
Food
Distribution
Distributed nationwide
HighCPSC·17215·2017-08-30
Dr. Brown's Natural Bottle and Dish Soap Recalled for Bacteria Risk
Handi-Craft is recalling Dr. Brown's Natural Bottle & Dish Soap because it may contain harmful bacteria. No injuries have been reported.
Product
Dr. Brown's Natural bottle and dish soap
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-3456-2017·2017-08-30
Lakeside Foods Recalls IQF Green Beans Due to Listeria Risk
Lakeside Foods, Inc. is recalling 1,856 cases of IQF green beans in 17 states due to potential Listeria monocytogenes contamination.
Product
IQF Green Beans, Keep Frozen. 11 varieties, packaged under the following brands and sizes: 1) Bountiful Harvest French Style Green Beans, 1 - 10lb carton/case; 2) GFS French Style Green Beans, 12 32oz (2lb) poly bags per case; 3) Bountiful Harvest Cut Green Beans, 1 20lb…
Category
Food
Distribution
17 states
HighFDA (Devices)·Z-3051-2017·2017-08-30
Medtronic ENT Suction Devices Recalled for Verification Failure
Medtronic Navigation is recalling 277 reusable ENT suction instruments because they fail pre-use verification checks. The devices are used with the StealthStation AxiEM surgical navigation system.
Product
Medtronic Straight Suction 9733449 EM ENT, reusable, Rx. The firm name on the label is Medtronic Navigation, Inc., Louisville, CO. The suction devices are part of a family of reusable ENT instruments that are used with the StealthStationTM AxiEM surgical navigation system. The…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-3398-2017·2017-08-30
Shatto Milk Co Recalls Unsalted Butter for Undeclared Milk Allergen
Shatto Milk Co is recalling 303 tubs of Cookin' Unsalted Butter because the product fails to disclose the presence of milk.
Product
Cookin' Unsalted Butter, packaged in 8 oz plastic tubs. Plant # 29-685 Osborn, MO.
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-3050-2017·2017-08-30
Alcon ORA System Recall for Incorrect IOL Power Measurements
Alcon is recalling 367 ORA Systems with VerifEye because a software error may cause incorrect intraocular lens power measurements during cataract surgery.
Product
ORA System with VerifEye, Catalog Number 8065998300 For use during intraocular lens surgery
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-3396-2017·2017-08-30
Shatto Milk Co Recalls Aromatic Garlic Butter for Undeclared Milk Allergen
Shatto Milk Co is recalling Aromatic Garlic Butter because the product fails to disclose the presence of milk, a major allergen.
Product
Aromatic Garlic Butter, packaged in 8 oz plastic tubs. Plant # 29-685 Osborn, MO.
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-3060-2017·2017-08-30
Shippert Medical Technologies Recalls Tissu-Trans Filtron 100 Due to Seal Integrity
Shippert Medical Technologies is recalling Tissu-Trans Filtron 100 units because the seal integrity of the sterile packages cannot be assured.
Product
Tissu-Trans Filtron 100, 3-TT-FILTRON 100. Product Usage: Intended for fat transfer and liposuction.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-3402-2017·2017-08-30
Shatto Milk Ice Cream Sandwiches Recalled for Undeclared Allergens
Shatto Milk Company is recalling 140 bags of ice cream sandwiches because they contain undeclared milk and wheat.
Product
Brownie, Chocolate Brownie and Vanilla, Ice Cream Sammich, packaged in 5 oz plastic bags. Shatto Milk Company, Osborn, MO.
Category
Food
Distribution
1 state
HighFDA (Food)·F-3401-2017·2017-08-30
Shatto Milk Ice Cream Sammich Recalled for Undeclared Allergens
Shatto Milk Company is recalling 126 bags of Ice Cream Sammich products due to undeclared milk and wheat allergens.
Product
Oatmeal, Oatmeal Raisin Cookie And Caramel Sea Salt, Ice Cream Sammich, packaged in 5 oz plastic bags. Shatto Milk Company, Osborn, MO.
Category
Food
Distribution
1 state