State

Kansas product recalls

73,737 recalls have nationwide distribution and so reach Kansas. 5,821 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total: 5,821
Critical: 1,053
Severe: 1,485
Most recent: 2026-10-28

Of the 5,821 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 1,485 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,821 recalls whose distribution notice names Kansas specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32951–32975 of 79558

HighFDA (Devices)·Z-0770-2020·2020-01-08
Carl Zeiss PLEX Elite 9000 Recalled for Electrical Shock Hazard
Carl Zeiss Meditec is recalling 151 PLEX Elite 9000 Swept-Source OCT devices because a design fault may expose operators to hazardous voltage when contacting the metal enclosure.
Product
The PLEX Elite 9000, a Swept-Source OCT [SS-OCT] - Product Usage: The PLEX Elite 9000 Swept-Source OCT [SS-OCT] is a non- contact, high resolution, wide field of view tomographic and biomicroscopic imaging device intended for in-vivo viewing, axial cross-sectional and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0748-2020·2020-01-08
Roche Recalls Accu-Chek Guide Blood Glucose Monitoring Systems Due to Power Issues
Roche Diabetes Care is recalling Accu-Chek Guide Blood Glucose Monitoring Systems due to potential power issues that may affect device performance.
Product
Blood Glucose Monitoring System, Model Number 07400926001 ACCU-CHEK GUIDE RETAIL KIT MG/DL - Product Usage: The Accu-Chek Guide Blood Glucose Monitoring System is intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and upper arm…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0752-2020·2020-01-08
Roche Recalls Accu-Chek Guide Blood Glucose Monitoring Systems Due to Power Issues
Roche Diabetes Care is recalling Accu-Chek Guide Blood Glucose Monitoring Systems due to potential power issues. The recall affects 452,392 units distributed in the US and internationally.
Product
Blood Glucose Monitoring System, Model Number 08313202001 ACCU CHEK GUIDE HCP SAMPLE LAUNCH BOX - Product Usage: The Accu-Chek Guide Blood Glucose Monitoring System is intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and upper…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0764-2020·2020-01-08
Villa Sistemi Medicali Recalls Apollo X-ray Tables Due to Chain Failure Risk
Villa Sistemi Medicali is recalling three Apollo X-ray tables because the angulation chain may fail early due to metal fatigue.
Product
Apollo, Model Numbers 9784100231, 9784120131, 9784130131 - Product Usage: Apollo table is a remote controlled X-ray system suitable for radiography and fluoroscopy examinations. The system is stationary mounted. The movements of the table and the tube stand are motorized and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0763-2020·2020-01-08
Villa Sistemi Medicali Recalls Juno DRF X-Ray Systems Due to Chain Failure
Villa Sistemi Medicali is recalling 46 Juno DRF x-ray systems because the angulation chain may fail early due to metal fatigue.
Product
Juno DRF, Model Number 709020 - Product Usage: General. multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0767-2020·2020-01-08
Medtronic Recalls O-arm O2 Imaging Systems Due to Belt Loosening
Medtronic is recalling 90 O-arm O2 Imaging Systems because a manufacturing issue may cause the gantry tractor motor drive belt to loosen, potentially rotating 3D images relative to the patient's physical position.
Product
O-arm" O2 Imaging System, Product Number/CFN: BI-700-02000
Category
Medical Device
Distribution
27 states
HighFDA (Devices)·Z-0681-2020·2020-01-08
DeWALT and Stanley Laser Distance Measurers Recalled for Excessive Radiation
Stanley Black & Decker is recalling specific DeWALT and Stanley laser distance measurers because they may emit laser radiation exceeding Class II safety limits.
Product
The products involved are DeWALT laser distance measurers, model numbers DW0165, DW0165S, DW0330S and Stanley Fatmax FMHT77506. These products were produced for DeWALT and Stanley by a contract manufacturer.
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0749-2020·2020-01-08
Roche Recalls Accu-Chek Guide Blood Glucose Meters Due to Power Issues
Roche Diabetes Care is recalling 21,094 Accu-Chek Guide Blood Glucose Monitoring Systems due to potential power issues. The recall covers units distributed in the US and 34 other countries.
Product
Blood Glucose Monitoring System, Model Number 07400942001 ACCU-CHEK GUIDE METER ONLY MG/DL US - Product Usage: The Accu-Chek Guide Blood Glucose Monitoring System is intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and upper…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0750-2020·2020-01-08
Roche Recalls Accu-Chek Guide Blood Glucose Monitoring Systems
Roche Diabetes Care is recalling specific Accu-Chek Guide Blood Glucose Monitoring Systems due to potential power issues.
Product
Blood Glucose Monitoring System, Model Number 08453071001 ACCU-CHEK GUIDE RETAIL KIT FCN MG/DL US - Product Usage: The Accu-Chek Guide Blood Glucose Monitoring System is intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0751-2020·2020-01-08
Roche Recalls Accu-Chek Guide Blood Glucose Monitoring Systems Due to Power Issues
Roche Diabetes Care is recalling 355,400 Accu-Chek Guide Blood Glucose Monitoring Systems due to potential power issues. The recall covers units distributed in the US and 33 other countries.
Product
Blood Glucose Monitoring System, Model Number 08453063001 ACCU-CHEK GUIDE SAMPLE KIT FCN MG/DL US - Product Usage: The Accu-Chek Guide Blood Glucose Monitoring System is intended to quantitatively measure glucose in fresh capillary whole blood from the fingertip, palm, and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0448-2020·2020-01-08
Sara Lee Frozen Pumpkin Spice Latte Pie Recalled for Undeclared Red Dye
Sara Lee Frozen Foods is recalling Chef Pierre Pumpkin Spice Latte Pies because they contain undeclared FD & C Red 40 dye.
Product
Chef Pierre 37 Ounce Pumpkin Spice Latte Pie, in foil pie pan with dome lid, frozen, 4 pies per wholesale case, with SKU number 09368 and UPC number 032100093682
Category
Food
Distribution
16 states
ModerateFDA (Drugs)·D-0647-2020·2020-01-08
Akorn Recalls Myorisan 20mg Capsules Due to Mispackaging Error
Akorn, Inc. is recalling Myorisan (isotretinoin) 20mg capsules because some cartons contained 40mg blister cards. The error was found in a customer complaint.
Product
MYORISAN (isotretinoin capsules, USP), 20mg, packaged in 30-count Capsules (3 x 10 Prescription Packs) per box, Rx only, Distributed by: VersaPharm Inc. - An Akorn Company, Lake Forset, IL 60045; NDC 61748-302-13.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0761-2020·2020-01-08
Abbott i-STAT cTnI Cartridges Recalled for Quality Check Code Issues
Abbott Point Of Care Inc. is recalling i-STAT cTnI cartridges because they may generate a higher than expected number of quality check codes.
Product
i-STAT cTnI cartridge
Category
Medical Device
Distribution
34 states
LowFDA (Devices)·Z-0771-2020·2020-01-08
Nidek Specular Microscope Recalled for Electromagnetic Noise Exceeding Standards
Nidek, Inc. is recalling 13 Specular Microscopes, Model CEM-530, because their electromagnetic noise exceeded the upper limit of the Electromagnetic Compatibility Standard.
Product
NIDEK Specular Microscope, Model CEM-530 - Product Usage: The device provides noncontact, high magnification image capture of endothelium enabling observation of the size and shape of cells. Information such as the number of endothelial cells, cell density, and cell area is…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0635-2020·2020-01-08
Lupin Recalls Bimatoprost Ophthalmic Solution Due to Impurity Specifications
Lupin Pharmaceuticals is recalling 2,130 bottles of Bimatoprost Ophthalmic Solution because an out-of-specification impurity was detected.
Product
Bimatoprost Ophthalmic Solution, 0.03%, For Use in the Eyes Only, Sterile, Rx Only, 7.5 mL bottle, Manufactured by: Lupin Limited, Pithampur (M.P.), INDIA, NDC: 68180-429-03.
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·20V005000·2020-01-06
Micro Bird Recalls 2015-2019 T-Series Buses for Fire Risk
Micro Bird is recalling 2015-2019 T-Series school buses because an oversized circuit breaker may cause wire overheating and fire.
Product
MICRO BIRD — MICRO BIRD T-SERIES TRANSIT BUS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V004000·2020-01-06
Micro Bird Recalls CT-Series Shuttle Buses Due to Fire Risk
Micro Bird is recalling 2015-2019 CT-Series shuttle buses because an oversized breaker may cause wire overheating and fire. Owners should contact the manufacturer for a free replacement.
Product
MICRO BIRD — MICRO BIRD CT-SERIES
Category
Vehicle
Distribution
Distributed nationwide
CriticalNHTSA·20V001000·2020-01-02
Subaru and Saab Vehicles Recalled for Air Bag Inflator Defect
Subaru is recalling specific 2003-2014 models and Saab 9-2X vehicles because passenger air bag inflators may explode due to humidity, posing a risk of serious injury or death.
Product
SUBARU — SUBARU, SAAB OUTBACK, BAJA, IMPREZA, LEGACY
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20E001000·2020-01-02
Takata Frontal Air Bag Inflators Recalled for Explosion Risk
Takata is recalling specific non-desiccated frontal air bag inflators used as interim remedies. These inflators may explode due to propellant degradation, posing a risk of serious injury or death.
Product
AIR BAGS:FRONTAL recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V003000·2020-01-02
Subaru and Saab Recall Vehicles Due to Air Bag Inflator Defect
Subaru is recalling specific 2003-2014 models and Saab 9-2X vehicles because passenger air bag inflators may explode, posing a risk of serious injury or death.
Product
SUBARU — SUBARU, SAAB OUTBACK, BAJA, IMPREZA, LEGACY
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V002000·2020-01-02
Subaru and Saab Recall Vehicles Due to Air Bag Inflator Defect
Subaru and Saab are recalling specific model years because passenger air bag inflators may explode due to humidity, posing a risk of serious injury.
Product
SUBARU — SUBARU, SAAB FORESTER, OUTBACK, BAJA, IMPREZA
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·PHA-01022020·2020-01-02
USDA Alerts on Sun Foods Egg Products Linked to Listeria Outbreak
USDA issued a public health alert for Sun Foods egg products containing ingredients from an FDA recall due to possible Listeria monocytogenes contamination.
Product
Sun Foods — FSIS Issues Public Health Alert for Products Associated with the FDA Almark Foods Recall Due to Possible Listeria Monocytogenes Contamination
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-0417-2020·2020-01-01
FDA Recalls Okami California Rolls for Listeria Contamination Risk
Fuji Food Products is recalling Okami brand 8pc California Rolls due to potential Listeria monocytogenes contamination. Consumers should not eat the product.
Product
Okami brand 8pc California Roll, SKU 28101
Category
Food
Distribution
31 states
CriticalFDA (Food)·F-0422-2020·2020-01-01
FDA Recalls Okami Spicy Supreme California Rolls for Listeria Risk
Fuji Food Products is recalling Okami brand 8pc Spicy Supreme California Rolls due to potential Listeria monocytogenes contamination.
Product
Okami brand 8pc Spicy Supreme California Roll, SKU 28104
Category
Food
Distribution
31 states
CriticalFDA (Food)·F-0414-2020·2020-01-01
Trader Joe's Tempura Shrimp Crunch Roll Recalled for Listeria Risk
Fuji Food Products is recalling Trader Joe's 8pc Tempura Shrimp Crunch Roll due to potential Listeria monocytogenes contamination.
Product
Trader Joe's 8pc Tempura Shrimp Crunch Roll, 8.5oz, SKU 513289
Category
Food
Distribution
31 states