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.

52426–52450 of 79649

HighFDA (Devices)·Z-1922-2016·2016-06-15
Baxter Recalls Actifuse Bone Void Fillers Due to Endotoxin Concerns
Baxter Healthcare is voluntarily recalling Actifuse ABX and MIS System bone void fillers because they may contain endotoxin levels above specification criteria.
Product
Actifuse ABX/Actifuse MIS System A bone void filler intended only for orthopedic applications as a filler for gaps and voids that are not intrinsic to the stability of the bony structure.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1915-2016·2016-06-15
GE Revolution CT Patient Table Recalled for Unintended Motion Risk
GE Healthcare is recalling Revolution CT Patient Tables because the cradle can descend on its own, posing a crushing risk to large patients.
Product
GE Revolution CT The system is intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications. The system is intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission projection data from the same axial…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1418-2016·2016-06-15
Werner Brand Sweet Hot Crunch Mix Recalled for Undeclared Milk Allergen
Werner Gourmet Meat Snacks is recalling Sweet Hot Crunch Mix because the label declares butter but fails to declare milk, a major allergen.
Product
Werner Brand Sweet Hot Crunch Mix, net wt. 2 oz, UPC 7 09972 80120 1. Werner Brand Sweet Hot Crunch Mix, net wt. 6 oz, UPC 7 09972 80100 3. The ingredients statement declared: "***BUTTER TOFFEE PEANUTS (PEANUTS, SUGAR, BUTTER, SALT)***". The label contains…
Category
Food
Distribution
19 states
HighFDA (Devices)·Z-1912-2016·2016-06-15
DePuy Synthes Flexible Shaft Reamers Recalled for Cytotoxicity Failure
Synthes (USA) Products LLC is recalling 244 DePuy Synthes 8.0 mm Flexible Shaft Reamers because they failed biological safety evaluations for cytotoxicity.
Product
DePuy Synthes 8.0 mm Flexible Shaft Reamer, 360 mm, Orthopedic manual surgical instrument. Part number 351.43
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1917-2016·2016-06-15
Zimmer Biomet Recalls Persona Trabecular Metal Tibial Plate Instruments
Zimmer Biomet is recalling specific Persona Trabecular Metal Tibial Plate Instruments and Modular Brackets due to incidents of radiolucent lines and loosening in implants.
Product
Persona Trabecular Metal Tibia; Persona Trabecular Metal Tibial Plate Instruments and Modular Brackets; Used to facilitate the implantation of joint replacement implants.
Category
Medical Device
Distribution
30 states
HighFDA (Devices)·Z-1925-2016·2016-06-15
Berchtold Recalls Surgical Table Cushions Due to Potential Staple Contamination
Berchtold Corp. is recalling 227 HybriGel surgical table cushions because they may contain staples that could appear on patient x-rays.
Product
Surgical Table Cushion (HybriGel Pads) HybrGel Pads are an optional accessory to the Operon Surgical Table. The pads may be attached to the base section with a Velcro fastener. The HybriGel pad shapes and variants can differ depending on the scope of the delivery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1423-2016·2016-06-15
Karlsburger Mesquite Seasoning Mix Recalled for Undeclared Soy Allergen
Karlsburger Foods is recalling 2 lb containers of Mesquite Seasoning Mix because they contain undeclared soy, a major food allergen.
Product
Karlsburger, Mesquite Seasoning Mix & Marinade, Item 46402, Net WT 2 lbs in plastic shaker jars.
Category
Food
Distribution
11 states
HighFDA (Devices)·Z-1937-2016·2016-06-15
Becton Dickinson Recalls 10 mL Syringes Due to Manufacturing Non-Conformities
Becton Dickinson is recalling 811,200 units of 10 mL syringes due to possible adulteration and non-conforming manufacturing practices.
Product
Henry Schein Single Use Syringe Luer-Lock, 10 mL, Intended for use by health care professionals for general purpose fluid aspiration/injection
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V438000·2016-06-15
Mercedes-Benz Recalls 2016 C300 Vehicles for Steering Software Error
Mercedes-Benz is recalling 2016 C300 4Matic vehicles because a software error may cause the electric power steering assist system to shut down, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ C300
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1691-2016·2016-06-15
Sedecal Mobile X-ray System Recalled for Software Defect
Sedecal USA is recalling 145 mobile x-ray systems in the US due to a software defect that may apply adult exposure parameters to newborns.
Product
Sedecal SA Mobile Diagnost w DR x-ray system
Category
Medical Device
Distribution
30 states
HighFDA (Devices)·Z-1936-2016·2016-06-15
Becton Dickinson Recalls 10 mL Syringes Due to Manufacturing Issues
Becton Dickinson is recalling 176,000 units of 10 mL syringes due to possible adulteration and non-conforming manufacturing practices.
Product
Henry Schein Single Use Syringe Luer-Lock, 10 mL, Intended for use by health care professionals for general purpose fluid aspiration/injection
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V439000·2016-06-15
Mercedes-Benz Recalls 2016 SLK and SL Models for Headlight Aim
Mercedes-Benz is recalling certain 2016 SLK and SL models because low-beam headlights may be aimed incorrectly, potentially reducing driver visibility.
Product
MERCEDES-BENZ — MERCEDES-BENZ SLK300, SL63, SL550, SLK350
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·16197·2016-06-15
Sony Recalls VAIO Laptop Battery Packs Due to Fire and Burn Hazards
Sony is recalling Panasonic lithium-ion battery packs for VAIO laptops because they can overheat, posing burn and fire hazards. No injuries have been reported.
Product
Panasonic battery packs used in Sony Electronics laptop computers
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·16V436000·2016-06-15
Nissan Recalls 2016 Leaf and Sentra for Passenger Air Bag Wiring Defect
Nissan is recalling specific 2016 Leaf and Sentra vehicles because a wiring harness connector may disconnect, preventing the passenger air bag from deploying in a crash.
Product
NISSAN — NISSAN LEAF, SENTRA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-1417-2016·2016-06-15
Werner Butter Toffee Peanuts Recalled for Undeclared Milk Allergen
Werner Gourmet Meat Snacks, Inc. is recalling Werner Brand Butter Toffee Peanuts because the labels declared butter but failed to declare milk as an ingredient.
Product
Werner Brand Butter Toffee Peanuts, net wt. 2.25 oz, UPC 7 09972 80113 3 Werner Brand Butter Toffee Peanuts, net wt. 6 oz., UPC 7 09972 80027 3 The ingredients statement declared: Peanuts, Sugar, Butter, Salt. The label contains an advisory statement Allergen…
Category
Food
Distribution
19 states
HighFDA (Drugs)·D-0956-2016·2016-06-15
Novo Nordisk Recalls Norditropin Pens Due to Delivery System Defect
Novo Nordisk is recalling 723 Norditropin FlexPro pens due to a potential assembly fault that may cause the pen to block during the air shot step.
Product
NORDITROPIN — NORDITROPIN (SOMATROPIN)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1914-2016·2016-06-15
Ortho VITROS 5600 System Recalled for Software Timing Anomaly
Ortho-Clinical Diagnostics is recalling VITROS 5600 systems due to a software defect that may cause sample aspiration errors, leading to inaccurate or contaminated test results.
Product
VITROS 5600 Integrated System, Catalog Number 6802413, Unique Device Identifier No. 10758750002740; and VITROS 5600 Integrated System (refurbished), Catalog Number 6802915, Unique Device Identifier No. 10758750007110; IVD.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1913-2016·2016-06-15
Ortho VITROS 3600 Immunodiagnostic System Recalled for Software Timing Anomaly
Ortho-Clinical Diagnostics is recalling VITROS 3600 systems due to a software timing anomaly that may cause the device to aspirate or dispense into unintended samples, potentially leading to erroneous or contaminated results.
Product
VITROS 3600 Immunodiagnostic System, Catalog Number 6802783,for use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1939-2016·2016-06-15
Stryker Recalls Maestro Air Motor Pneumatic Cranial Drill Units
Stryker is recalling 189 Maestro Air Motor pneumatic cranial drill units because grease buildup may cause the orange grease to leak and contaminate surgical wounds.
Product
Maestro Air Motor Pneumatic cranial drill motor. The Maestro Air Pneumatic System is a pneumatically operated surgical instrument system. The pneumatic motor provides power to operate removable rotating surgical cutting tools and their accessories.
Category
Medical Device
Distribution
22 states
ModerateFDA (Devices)·Z-1943-2016·2016-06-15
DePuy Synthes Recalls Norian Drillable Inject Due to Labeling Error
DePuy Synthes is voluntarily recalling Norian Drillable Inject 5 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 5 CC-Sterile; catalog # 07.704.005S 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-1697-2016·2016-06-15
Ellipse ND: YAG Laser Applicator Recalled for Missing Calibration Instructions
Ellipse A/S is recalling 14 Ellipse ND: YAG Laser applicators because they lack required instructions for calibration procedures and schedules.
Product
Ellipse ND: YAG Laser applicator for Ellipse Multiflex Medical Laser Products.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1932-2016·2016-06-15
Beckman Coulter Uric Acid Reagent Recalled for False Low Results
Beckman Coulter is recalling Uric Acid reagent (OSR6x98) because Dipyrone may cause erroneous, false low results in assays.
Product
Uric Acid, Catalog No. OSR6x98 Product Usage:Uric acid OSR6x98 is intended as a System reagent for the quantitative determination of Uric Acid in human serum, heparinized plasma and urine on Beckman Coulter AU analyzers.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1934-2016·2016-06-15
Beckman Coulter Recalls Triglyceride Assay Due to Dipyrone Interference
Beckman Coulter is recalling Triglyceride OSR6x118 assays because Dipyrone may cause false low results.
Product
Triglyceride, Catalog No. OSR6x118 Product Usage:Triglyceride OSR6x118 is intended as an Enzymatic colour test for the quantitative determination of triglyceride in human serum and plasma on Beckman Coulter AU analyzers.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1911-2016·2016-06-15
Integrated Science Systems Recalls Sure Vue Staph Identification Kits
Integrated Science Systems is recalling Sure Vue Staph kits due to customer complaints of weak reactions and false negative results.
Product
Sure Vue Color Staph 150T, Sure Vue Color Staph 300T, Sure Vue SELECT Staph, biokit SELECT Staph 75T The product is used as an aid in the identification of Staphylococcus aureus from Culture
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1919-2016·2016-06-15
Synthes Rapid Resorbable Orbital Floor Plate Recalled for Labeling Errors
Synthes (USA) Products LLC is recalling 19 units of 1.5 mm Rapid Resorbable Orbital Floor Plates due to potential expiration date discrepancies on outer packaging labels.
Product
1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 30 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