State

Kansas product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42651–42675 of 79631

HighFDA (Devices)·Z-0906-2018·2018-03-14
Synthes Recalls 2.5 mm Titanium Calibrated Reaming Rods Due to Sterility Concerns
Synthes (USA) Products LLC is recalling 63 units of 2.5 mm Titanium Calibrated Reaming Rods because potential gaps in the package seal may have compromised product sterility.
Product
2.5 mm Titanium Calibrated Reaming Rod, 850 mm, Part Number: 359.083S Reaming Rods are intended for guiding of reamers during orthopedic surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0899-2018·2018-03-14
Heartland Coca-Cola Recalls Cans with Sharp Edges
Heartland Coca-Cola Bottling Company is recalling specific cans of Coca-Cola, Original Taste, because sharp edges were observed that could cause cuts to consumers' mouths.
Product
Coca-Cola, Original Taste, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
Category
Food
Distribution
6 states
HighFDA (Food)·F-0891-2018·2018-03-14
Heartland Coca-Cola Recalls Diet Coke Lime Cans Due to Sharp Edges
Heartland Coca-Cola Bottling Company is recalling Diet Coke Lime cans because sharp edges were observed, posing a risk of cuts to consumers' mouths.
Product
Diet Coke Lime, 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-0851-2018·2018-03-14
Bausch & Lomb Recalls LaserEdge Ophthalmic Knives Due to Dull Blades
Bausch & Lomb Inc is voluntarily recalling 1,236,749 LaserEdge ophthalmic knives because an atypical volume of complaints indicates dull blades. The recall affects products lacking specific electro-polish and penetration force testing.
Product
LASEREDGE Knives, CRESCENT BLADE STRAIGHT BEVEL UP STR (6/BOX), REF/PRODUCT CODE E7500, STERILE, Rx Only Product Usage: The LaserEdge Knives are intended for ophthalmic surgery. There is no therapeutic use and they are available to surgeons for use in procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0849-2018·2018-03-14
DePuy Concorde Lift Torque Limiting Handle Recalled for Breakage Risk
DePuy Orthopaedics is recalling 130 Concorde Lift Torque Limiting Handles due to a potential for intra-operative breakage of driver tips.
Product
Concorde Lift Torque Limiting Handle. Must be used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0904-2018·2018-03-14
Synthes Reaming Rods Recalled for Potential Sterility Seal Defects
Synthes (USA) Products LLC is recalling 960 sterile 3.0 mm Reaming Rods because package seal defects may compromise sterility.
Product
3.0 mm Reaming Rod, with straight ball tip, 950 mm, sterile, Part Number: 351.76S Reaming Rods are intended for guiding of reamers during orthopedic surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0884-2018·2018-03-14
Emerald Glazed Walnuts Recalled for Undeclared Nuts
Snyder's-Lance is voluntarily recalling 6.5 oz Emerald brand Glazed Walnuts due to undeclared peanuts, almonds, cashews, and pecans.
Product
Emerald brand Glazed Walnuts; Net WT. 6.5 OZ; Re-sealable pouch
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0902-2018·2018-03-14
Synthes Recalls 2.5 mm Reaming Rods Due to Potential Sterility Loss
Synthes (USA) Products LLC is recalling 216 units of 2.5 mm Reaming Rods because package seal defects may have compromised sterility.
Product
2.5 mm Reaming Rod, Ball tip with extension, 950 mm, sterile, Part Number: 351.707S Reaming Rods are intended for guiding of reamers during orthopedic surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0893-2018·2018-03-14
Heartland Coca-Cola Recalls Mello Yola Cans Due to Sharp Edges
Heartland Coca-Cola Bottling Company is recalling Mello Yola citrus-flavored soda cans because sharp edges on the cans could cut consumers' mouths.
Product
Mello Yello, Citrus Flavored Soda, 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-0905-2018·2018-03-14
Synthes 2.5 mm Guide Rods Recalled for Potential Sterility Loss
Synthes (USA) Products LLC is recalling 21 sterile 2.5 mm Guide Rods due to potential package seal defects that may compromise sterility.
Product
2.5 mm Guide Rod, with smooth tip, 950 mm, sterile, Part Number: 355.042S Reaming Rods are intended for guiding of reamers during orthopedic surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0911-2018·2018-03-14
VITROS DAT Performance Verifier I recalled due to labeling issue
Ortho-Clinical Diagnostics is recalling 349 units of VITROS DAT Performance Verifier I because the storage labeling is incorrect, which may cause lower than expected test results.
Product
VITROS Chemistry Products DAT Performance Verifier I in vitro diagnostic
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0858-2018·2018-03-14
Bausch & Lomb Recalls LaserEdge Ophthalmic Knives Due to Dull Blades
Bausch & Lomb is voluntarily recalling 1,236,749 LaserEdge ophthalmic knives nationwide due to an atypical volume of complaints regarding dull blades.
Product
LASEREDGE Knives, 19 GAUGE MVR BLADE (6/BOX), REF/PRODUCT CODE E7519, STERILE, Rx Only Product Usage: The LaserEdge Knives are intended for ophthalmic surgery. There is no therapeutic use and they are available to surgeons for use in procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0896-2018·2018-03-14
Medtronic Recalls Unimplanted SynchroMed II Pumps Due to Motor Stall Risk
Medtronic is recalling unimplanted SynchroMed II Model 8637 pumps to address a design flaw that can cause motor stalls due to corrosion.
Product
Medtronic Synchromed II Model 8637 supplied in 20mL and 40 mL reservoir size and a catheter. Product Usage: The implantable Model 8637 SynchroMed II programmable pump is part of an infusion system that stores and delivers a prescribed drug to a specific site. The implanted…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0850-2018·2018-03-14
Philips Network Firewall Recall Due to Defective Clock Component
Philips is recalling 332 network firewalls used with IntelliVue systems due to a defective clock component that may cause loss of connection.
Product
Philips Network Firewall (Cisco ASA 5506), Model # 867098
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0848-2018·2018-03-14
DePuy Concorde Lift Driver Shaft Recalled for Potential Breakage
DePuy Orthopaedics is recalling 130 units of the Concorde Lift Driver Shaft AO due to a potential for intra-operative breakage of driver tips.
Product
Concorde Lift Driver Shaft AO. Used with supplemental internal spinal fixation systems that have been cleared for use in the lumbar spine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0898-2018·2018-03-14
Heartland Coca-Cola Recalls Orange Fanta Cans Due to Sharp Edges
Heartland Coca-Cola Bottling Company is recalling Orange Fanta cans because sharp edges on the cans could cause cuts to consumers' mouths.
Product
Orange Fanta, Orange soda, Naturally flavored, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-0892-2018·2018-03-14
Bausch & Lomb Recalls LaserEdge Ophthalmic Knives Due to Dull Blade Complaints
Bausch & Lomb Inc Irb is voluntarily recalling LASEREDGE Knives intended for ophthalmic surgery because of an atypical volume of complaints regarding dull blades.
Product
LASEREDGE Knives, 2.0MMX2.2MM TRAPEZOID ANGLED GUARDED (6/BOX), REF/PRODUCT CODE E7601G, STERILE, Rx Only Product Usage: The LaserEdge Knives are intended for ophthalmic surgery. There is no therapeutic use and they are available to surgeons for use in procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0918-2018·2018-03-14
Zimmer Biomet Flexible Shaft Instruments Recalled for Infection Risk
Zimmer Biomet is recalling 457 Flexible Shaft instruments because they may not clean adequately, posing a risk of infection.
Product
Flexible Shaft hip and anatomical shoulder instrument used for preparation of bone in Trauma, Hip and Shoulder surgeries.; Model Number: 75.80.04
Category
Medical Device
Distribution
32 states
HighFDA (Food)·F-0904-2018·2018-03-14
Fresca Citrus Soda Recalled Due to Sharp Can Edges
Heartland Coca-Cola Bottling Company is recalling Fresca Original Citrus Sparkling Flavored Soda cans because sharp edges were observed that could cause cuts to consumers' mouths.
Product
Fresca, Original Citrus Sparkling Flavored Soda, 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
Category
Food
Distribution
6 states
HighFDA (Food)·F-0905-2018·2018-03-14
Heartland Coca-Cola Recalls Strawberry Fanta Cans Due to Sharp Edges
Heartland Coca-Cola Bottling Company is recalling Strawberry Fanta cans because sharp edges were observed, posing a risk of cuts to consumers' mouths.
Product
Strawberry Fanta, Strawberry Flavored Soda, 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-0910-2018·2018-03-14
Roche cobas 8000 Modular Analyzer Recall for Operator Injury Prevention
Roche Diagnostics is recalling 245 cobas 8000 c 502 modules to add a warning to the manual, preventing operator injury during maintenance.
Product
cobas 8000 Modular Analyzer Series; Part Numbers: 1. 05964067001 cobas 8000 c 502 module
Category
Medical Device
Distribution
51 states
HighFDA (Food)·F-0900-2018·2018-03-14
Coca-Cola Zero Sugar Cans Recalled for Sharp Edges
Heartland Coca-Cola Bottling Company is recalling specific lots of Coca-Cola Zero Sugar cans due to sharp edges that could cause mouth cuts.
Product
Coca-Cola, Zero Sugar, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
Category
Food
Distribution
6 states
HighFDA (Food)·F-0907-2018·2018-03-14
Dr Pepper Cans Recalled Due to Sharp Edges Causing Potential Cuts
Heartland Coca-Cola Bottling Company is recalling Dr Pepper 12 oz cans because sharp edges were observed, posing a risk of cuts to consumers' mouths.
Product
Dr Pepper, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of Dr Pepper Company, Plano, TX
Category
Food
Distribution
6 states
HighCPSC·18122·2018-03-14
Radio Flyer Recalls Electric Wagons Due to Unintentional Motor Activation
Radio Flyer is recalling about 5,000 eWagons because improper wiring can cause the motor to activate unintentionally, posing an injury hazard.
Product
Children's eWagons
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-0896-2018·2018-03-14
Heartland Coca-Cola Recalls Caffeine Free Coke Zero Cans Due to Sharp Edges
Heartland Coca-Cola Bottling Company is recalling Caffeine Free Coke Zero cans because sharp edges were observed that could cause cuts to consumers' mouths.
Product
Caffeine Free Coke Zero, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA
Category
Food
Distribution
6 states