State

Kansas product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55876–55900 of 79655

HighFDA (Devices)·Z-0156-2016·2015-10-28
Smith & Nephew MOSAICPLASTY Harvesting System Recalled for Packaging Breach
Smith & Nephew is recalling MOSAICPLASTY DP- Disposable Harvesting Systems because a breach in the packaging compromised the device's sterility.
Product
Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 4.5 mm, Sterile Part Number: 7209235 Intended Use: For arthroscopic (knee and ankle) and open osteochondral grafting fix for osteochondral (cartilage) defects.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0049-2016·2015-10-28
JBN Chocolate Whey Superior Recalled for Undeclared Milk Allergen
Nutrition Resource Services, Inc. is recalling JBN Chocolate Whey Superior because the product is not labeled as containing milk, a major allergen.
Product
JBN (Just Be Natural) Chocolate Whey Superior NET WT. 29.6 oz. (1.85 lb) 840g and NET WT. 88.9 oz. (5.55 lb) 2,520g - DIETARY SUPPLEMENT, packaged in plastic bottles, UPC codes: 655455020112, 655455001692, MANUFACTURED BY NRS -Nutrition Resource Services, Inc. DISTRIBUTED BY…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0039-2016·2015-10-28
JBN Growtein Protein Powder Recalled for Unlabeled Milk Allergen
Nutrition Resource Services is recalling JBN Growtein Growth Protein because whey-based products are not labeled as containing milk.
Product
JBN (Just Be Natural) Growtein Growth Protein Vanilla Cream NET WT. 97 oz. (6 lb) 2750g - DIETARY SUPPLEMENT packaged in plastic bottles, UPC code: 655455001661, MANUFACTURED BY NRS -Nutrition Resource Services, Inc. DISTRIBUTED BY JBN - Just Be Natural; INGREDIENTS: Whey…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0044-2016·2015-10-28
JBN Unflavored Whey Isolate Recalled for Undeclared Milk Allergen
Nutrition Resource Services, Inc. is recalling JBN Unflavored 100% Whey Isolate because the product is not labeled as containing milk, posing a risk to individuals with milk allergies.
Product
JBN (Just Be Natural) Unflavored 100% WHEY ISOLATE Enhanced Performance Nutrition; UPC code: 655455017594, MANUFACTURED BY NRS -Nutrition Resource Services, Inc. DISTRIBUTED BY JBN -Just Be Natural NET WT. 27.5 oz. (1.72 lb) 780g - DIETARY SUPPLEMENT; packaged in plastic…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0054-2016·2015-10-28
Hospira Recalls Amidate Etomidate Injection Due to Degradation Impurities
Hospira Inc. is recalling 24,100 syringes of Amidate (Etomidate Injection) because stability testing confirmed out-of-specification degradation products.
Product
Amidate (Etomidate Injection, USP), 40 mg/20 mL (2 mg/mL), LifeShield, 20 mL, Glass Abboject Syringe with male luer lock adapter, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-8060-29
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0143-2016·2015-10-28
ConForMIS iDuo Knee Replacement Recalled for Ethylene Glycol Residue
ConforMIS, Inc. is recalling 12 units of the iDuo Knee Bicompartmental Knee Replacement System because they may contain small amounts of ethylene glycol residue.
Product
ConForMIS iDuo Knee Bicompartmental Knee Replacement System , iDUO G2, Right Medial Catalog Number: M57230600220 (US) M5723INT0600220 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0152-2016·2015-10-28
Smiths Medical Recalls Port-A-Cath Needles Due to Incorrect Labeling
Smiths Medical ASD, Inc. is recalling Port-A-Cath Plastic Hub Needles from Lot 46262 because the lid stock labels contain incorrect part numbers, descriptions, and images.
Product
PORT-A-CATH Plastic Hub Needles, 0.9mm (20G) x 19mm (3/4 in.) 90-degree. REF 21-2287-24 The Plastic hub PORT-A-CATH (PAC) needles are intended to access the implantable portal system for the purpose of infusion or withdrawal of fluids. These PAC needles can be used with…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0147-2016·2015-10-28
ConFormis iTotal Knee Replacement System Recalled for Ethylene Glycol Residue
ConforMIS is recalling 110 units of the iTotal Posterior Stabilized Knee Replacement System because they may contain small amounts of ethylene glycol residue.
Product
ConFormis iTotal Posterior Stabilized Knee Replacement System- ITOTAL PS-IPOLY- IMPLANT KIT-LEFT and ITOTAL PS-IPOLY-IMPLANT KIT-RIGHT Catalog Number:TPS1111111
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0137-2016·2015-10-28
Biomet Thinflap System Cases Recalled Due to Lid Opening Difficulty
Biomet Microfixation is recalling 5 Thinflap System Cases because the lids require excessive force to open.
Product
Thinflap System Case The cases hold surgical instrumentation in place during handling and storage.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0134-2016·2015-10-28
Synthes Recalls Spinal Pedicle Fixation Rods Due to Finishing Process Error
Synthes (USA) Products LLC is recalling 492 spinal pedicle fixation rods because they were produced using a bead blast process not identified in the manufacturing specification.
Product
5.0mm Unit Rod 270mm, 5.0mm Unit Rod 290mm, 5.0mm Unit Rod 310mm, 5.0mm Unit Rod 330mm, 5.0mm Unit Rod 350mm, 5.0mm Unit Rod 370mm, 5.0mm Unit Rod 390mm, 5.0mm Unit Rod 410mm, 5.0mm Unit Rod 430mm, 5.0mm Unit Rod 450mm; Orthosis, Spinal, Pedicle fixation Intended to…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0144-2016·2015-10-28
ConFormis iTotal CR Knee Replacement System Recalled for Ethylene Glycol Residue
ConforMIS, Inc. is recalling 3 units of the iTotal CR Knee Replacement System because they may contain small amounts of ethylene glycol residue.
Product
ConFormis iTotal CR Knee Replacement System- ITOTAL CR - IPOLY - IMPLANT KIT UNCAPTURED - LEFT ITOTAL CR - IPOLY - IMPLANT KIT UNCAPTURED - RIGHT Catalog Number: TCR1111111
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0035-2016·2015-10-28
JBN Chocolate Whey Protein Powder Recalled for Missing Milk Labeling
Nutrition Resource Services is recalling JBN Chocolate Confidence Nutritional Support for Bariatric Surgery because the whey protein product is not labeled as containing milk.
Product
JBN (Just Be Natural) Chocolate Confidence Nutritional Support for Bariatric Surgery 25G 100% WHEY ISOLATE; NET WT. 43.4 oz. (2.7 lb) 1,230g - packaged in plastic bottles, UPC code: 655455018225, DIETARY SUPPLEMENT MANUFACTURED BY NRS -Nutrition Resource Services, Inc.…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0146-2016·2015-10-28
ConFormis iTotal CR Knee Replacement System Recalled for Ethylene Glycol Residue
ConforMIS, Inc. is recalling 348 units of the iTotal CR Knee Replacement System because they may contain small amounts of ethylene glycol residue.
Product
ConFormis iTotal CR Knee Replacement System- iTOTAL CR, Right Knee Catalog Number: M57250600020 (US) M5725INT0600020 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0153-2016·2015-10-28
OneTray Sealed Sterilization Containers Recalled for Incorrect Labeling
Innovative Sterilization Technologies LLC is recalling OneTray Sealed Sterilization Containers because the labels list the wrong steam sterilization time.
Product
OneTray Sealed Sterilization Containers Product Usage: A rigid sterilization container used to steam sterilize medical devices
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0149-2016·2015-10-28
Natus neoBLUE 3 Phototherapy System Recalled for Intensity Documentation
Natus Medical is recalling 4,560 neoBLUE 3 Phototherapy systems because the instruction manuals did not accurately reflect the cleared intensity settings.
Product
Natus neoBLUE 3 Phototherapy system or Neonatal Phototherapy, Catalogue Part Number: 010066; Top Assembly Part Number: 001103
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0136-2016·2015-10-28
Biomet Neuro Combo Set Case Lid Requiring Excessive Force Recalled
Biomet Microfixation is recalling 37 Neuro Combo Set Cases because the lids require excessive force to open.
Product
Neuro Combo Set Case The cases hold surgical instrumentation in place during handling and storage.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0135-2016·2015-10-28
Philips MRI Systems Recalled for Incorrect Cross-Reference Lines in Spine Imaging
Philips Medical Systems is recalling specific MRI systems due to a software defect that may cause cross-reference lines to be positioned incorrectly in spine clinical workflows.
Product
All Philips Ingenia, Intera, Achieva and Multiva MR systems using R5.1i and R5.1 .2 version of software. Indicated for use as a diagnostic device. It can produce cross-sectional images, spectroscopic images and/or spectra in any orientation of the internal structure of the…
Category
Medical Device
Distribution
22 states
ModerateFDA (Devices)·Z-0140-2016·2015-10-28
ConForMIS iUNI Knee Replacement Recalled for Ethylene Glycol Residue
ConForMIS is recalling 6 units of the iUNI Unicondylar Knee Replacement System due to potential ethylene glycol residue.
Product
ConForMIS iUNI Unicondylar Knee Replacement System iUNI G2, Right Lateral Catalog Number: M57220600240 (US) M5722INT0600240 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0139-2016·2015-10-28
ConForMIS Knee Replacement System Recalled for Ethylene Glycol Residue
ConforMIS, Inc. is recalling 71 units of the ConForMIS Unicondylar Knee Replacement System iUNI G2, Left Medial due to potential small amounts of ethylene glycol residue.
Product
ConForMIS Unicondylar Knee Replacement System iUNI G2, Left Medial Catalog Number: M57220600210(US) M5722INT0600210 (OUS)
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0053-2016·2015-10-28
Donnatal Prescription Drug Recalled for Incorrect Ingredient Labeling
Rx PAK is recalling Donnatal tablets because the label incorrectly lists Scopolamine Hydrocodone instead of Scopolamine Hydrobromide.
Product
DONNATAL — DONNATAL (PHENOBARBITAL, HYOSCYAMINE SULFATE, ATROPINE SULFATE, SCOPOLAMINE HYDROBROMIDE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·15V712000·2015-10-27
Ford Recalls 2009-2010 Edge and Lincoln MKX for Fuel Tank Leak
Ford is recalling 2009-2010 Edge and Lincoln MKX vehicles in 22 states and D.C. because salt water corrosion may cause the fuel tank to leak, increasing fire risk.
Product
FORD — FORD, LINCOLN EDGE, MKX
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V709000·2015-10-27
Mercedes-Benz Recalls 2016 GLE450 and GLE63 Due to Drive Shaft Bolt Issue
Mercedes-Benz is recalling 2016 GLE450 and GLE63 coupes because rear drive shaft bolts may loosen, causing the shaft to separate and the vehicle to stall.
Product
MERCEDES-BENZ — MERCEDES-BENZ GLE450, AMG GLE63
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V708000·2015-10-27
Fontaine Recalls 2014-2016 Revolution Flat Trailers for Structural Weld Cracks
Fontaine Trailer Company is recalling 2014-2016 Revolution flat trailers because structural welds may crack, potentially causing a crash.
Product
FONTAINE — FONTAINE REVOLUTION
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V711000·2015-10-27
Mercedes-Benz Recalls Vehicles Due to Air Bag Control Unit Corrosion
Mercedes-Benz is recalling 2008-2010 C300, C350, C63, and GLK350 vehicles because the air bag control unit may corrode and malfunction, potentially causing air bags to deploy unexpectedly or fail to deploy.
Product
MERCEDES BENZ — MERCEDES BENZ, MERCEDES-BENZ C63, GLK350, C300, C350
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·16018·2015-10-27
LaRose Recalls Peanuts Flying Ace Ride-On Toys for Choking Hazard
LaRose Industries is recalling Peanuts Flying Ace ride-on toys because blue hubcaps can detach, posing a choking hazard to young children.
Product
Peanuts Flying Ace Ride-On Toys
Category
Consumer Product
Distribution
Distributed nationwide