State

Kansas product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35501–35525 of 79559

ModerateFDA (Devices)·Z-2077-2019·2019-07-31
Getinge Recalls Seven PulsioFlex Monitoring Systems Due to Error Messages
Getinge US Sales LLC is recalling seven PulsioFlex Monitoring Systems because they display an internal error message requiring restart or service.
Product
PulsioFlex Monitoring System, Part Number: 6882747, Model Number: PC400 3 R0. Usage: The PulsioFlex Monitoring System is indicated in patients where cardiovascular and circulatory volume status monitoring is necessary. If a patient s biometric data are entered, the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2082-2019·2019-07-31
Medical Intelligence Recalls iGuide System Software Due to False Verification Alerts
Medical Intelligence Medizintechnik GmbH is recalling iGuide System software versions 2.2.0, 2.2.1, and 2.2.2 because the Constant Correlation Check may incorrectly demand verification scans.
Product
IGuide System, software versions: 2.2.0, 2.2.1, 2.2.2 Product Usage: Linear Accelerator. The intended use of the device is the control of accurate patient positioning with assistance of a 30 Tracking System in a radiotherapy environment.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2014-2019·2019-07-31
Siemens AXIOM Artis MP X-ray Generator Recall for Power Supply Issue
Siemens is recalling 24 AXIOM Artis MP units because a power supply tolerance issue may cause generator failure, preventing X-ray procedures.
Product
AXIOM Artis MP, Model Number 5904466
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1992-2019·2019-07-31
Abbott C4 In Vitro Diagnostic Assay Recall for Instruction Manual Updates
Abbott Laboratories is recalling 8,037 C4 in vitro diagnostic assay kits to update the Instructions for Use (IFU) regarding reagents and specimen handling.
Product
C4 is an in vitro diagnostic assay for the quantitative determination of C4 in human serum or plasma. Antigen in the sample bonds to the specific antibody in the reagent, forming an immune complex. The immune complex causes an increase in light scattering, measured by reading…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2000-2019·2019-07-31
Terumo Sur-vet Needle Recall Due to Potential Sterility Compromise
Terumo Medical Corporation is recalling 638,000 Sur-vet Needles due to a potential loss of package integrity that may compromise sterility.
Product
Terumo Sur-vet Needle, 22G x 3/4", Product Code 100215
Category
Medical Device
Distribution
12 states
ModerateFDA (Devices)·Z-2007-2019·2019-07-31
Becton Dickinson Recalls 3mL Luer-Lok Syringes With Incorrect Scale Markings
Becton Dickinson is recalling 3mL Luer-Lok syringes because the scale markings were printed incorrectly, resulting in missing or partially printed numbers and lines.
Product
3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573
Category
Medical Device
Distribution
13 states
ModerateFDA (Drugs)·D-1502-2019·2019-07-31
Pharma-Natural Recalls Lid O Creme Due to Manufacturing Violations
Pharma-Natural Inc. is recalling Lid O Creme topical analgesic cream because it was manufactured with current good manufacturing practice violations, including lack of process validation.
Product
Lid O Creme (Lidocaine HCL 4% and Menthol 1%) Topical Analgesic Cream, 2.5 Oz (71 g) roll on bottle, Manufactured & Distributed by: Pharma Natural, Inc. Hialeah, FL 33016, NDC 63788-111-25.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2012-2019·2019-07-31
Siemens AXIOM Artis FC X-ray Generator Recall for Power Supply Defect
Siemens is recalling five AXIOM Artis FC units due to a power supply tolerance issue that may cause generator failure and prevent X-ray imaging.
Product
AXIOM Artis FC, Model Number 5904433
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1509-2019·2019-07-31
Temozolomide Capsules Recalled for Potential Cross-Contamination with Beta-Lactam Products
Deva Holding AS is recalling Temozolomide capsules due to manufacturing deviations that allowed possible cross-contamination with beta-lactam products.
Product
TEMOZOLOMIDE — TEMOZOLOMIDE (TEMOZOLOMIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1494-2019·2019-07-31
Pharma-Natural Recalls Army Health Pain Reliever Roll-On for CGMP Violations
Pharma-Natural Inc. is recalling Army Health Pain Reliever Roll-On bottles due to manufacturing process violations. The product was distributed in Florida and Texas.
Product
ARMY HEALTH With CURCUMIN (Menthol 3.00%) Pain Reliever Roll-On, 2.5 FL OZ (73ML) roll on bottle, Manufactured exclusively for: Crossover Telecom, LLC., P.O. Box 520248, Miami, FL 33122, UPC 8 50993 00408 6.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2034-2019·2019-07-31
Siemens Artis zeego X-ray Generator Recall for Power Supply Tolerance Issue
Siemens Medical Solutions is recalling 117 Artis zeego units due to a power supply tolerance issue that can cause generator failure and prevent X-ray imaging.
Product
Artis zeego, Model Number 10280959
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2062-2019·2019-07-31
Merge PACS Software Recalled for Mammography Image Display Errors
Merge Healthcare is recalling specific versions of Merge PACS software because mammography images may not display in the correct reverse chronological order.
Product
Merge PACS versions 7.3, 7.3.1, 8.0 and 8.0.1
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2032-2019·2019-07-31
Siemens Artis zee floor MN X-ray generator recall
Siemens is recalling 23 Artis zee floor MN units due to a power supply tolerance issue that may cause generator failure and prevent X-ray imaging.
Product
Artis zee floor MN, Model Number 10094142
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1495-2019·2019-07-31
FDA Recalls Oliver's Harvest CBD+Lidocaine Cream for Manufacturing Violations
Pharma-Natural Inc. is recalling Oliver's Harvest CBD+Lidocaine HCL 4% Pain Relief Cream due to current good manufacturing practice violations, including lack of process and cleaning validation.
Product
Oliver's Harvest CBD+Lidocaine HCL 4% Pain Relief (Lidocaine HCL 4%) Topical Analgesic Cream, 4 OZ (113.4 g) bottle with pump, Distributed by: Coast to Coast Natural, Inc., Wellington, FL 33414, NDC 63766-119-04.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1988-2019·2019-07-31
Abbott Immunoglobulin A Diagnostic Assay Recalled for Instruction Manual Errors
Abbott Laboratories is recalling 12,995 Immunoglobulin A diagnostic kits because the instructions for use contained errors in the reagents and specimen handling sections.
Product
Immunoglobulin A is an in vitro diagnostic assay for the quantitative determination of immunoglobulin A in human serum or plasma. Antigen in the sample bonds to the specific antibody in the reagent, forming an immune complex. The immune complex causes an increase in light…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1994-2019·2019-07-31
Abbott Apolipoprotein B Assay Recalled for Instruction Manual Updates
Abbott Laboratories is recalling 2,273 Apolipoprotein B in vitro diagnostic kits because the Instructions for Use (IFU) required updates to reagent and specimen handling sections.
Product
Apolipoprotein B is an in vitro diagnostic assay for the quantitative determination of apolipoprotein B in human serum or plasma. Antibodies to apolipoprotein B combine with apolipoprotein B in the sample to form insoluble immune complexes. The immune complexes cause an…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2008-2019·2019-07-31
Becton Dickinson Recalls 3mL Safety-Lok Syringes Due to Incorrect Scale Markings
Becton Dickinson is recalling 428,800 3mL Safety-Lok Syringes because the scale markings were printed incorrectly, resulting in missing or partially printed numbers and lines.
Product
3mL Safety-Lok Syringe, Catalog Number 309606, UDI 30382903096061
Category
Medical Device
Distribution
13 states
ModerateFDA (Devices)·Z-2020-2019·2019-07-31
Siemens AXIOM Artis dFC X-ray Generator Recall for Power Supply Issue
Siemens is recalling 148 AXIOM Artis dFC units because a power supply defect may cause the X-ray generator to fail during procedures.
Product
AXIOM Artis dFC, Model Number 7412807
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1493-2019·2019-07-31
Pharma-Natural Recalls AbeeMed Cream Due to Manufacturing Violations
Pharma-Natural Inc. is recalling AbeeMed cream because it was manufactured with current good manufacturing practice violations, including a lack of process and cleaning validation.
Product
AbeeMed cream (Menthol 1.48% and Histamine DHCL 0.05%), 2 OZ jar, Manufactured exclusively for: Cas, P.O. Box 520248, Miami, FL 33152, UPC 8 50993 00402 4.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1501-2019·2019-07-31
Lido E.R. Lidocaine Cream Recalled for Manufacturing Violations
Pharma-Natural Inc. is recalling Lido E.R. Lidocaine Cream due to current good manufacturing practice violations, including lack of process and cleaning validation.
Product
Lido E.R. (Lidocaine HCL 4%) Pain Relieving Topical Analgesic Cream, 4 oz (113 g) jar, Distributed by Diabetic Supply of Suncoast, Inc., P.O. Box 2102, Vega Alta, PR 00692, NDC 63788-115-04.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1990-2019·2019-07-31
Abbott Immunoglobulin M Diagnostic Assay Recalled for Instruction Manual Errors
Abbott Laboratories is recalling 9,586 Immunoglobulin M diagnostic kits because the instructions for use contained errors in the reagents and specimen handling sections.
Product
Immunoglobulin M is an in vitro diagnostic assay for the quantitative determination of immunoglobulin M in human serum or plasma. Antigen in the sample bonds to the specific antibody in the reagent, forming an immune complex. The immune complex causes an increase in light…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1995-2019·2019-07-31
Abbott Transferrin Assay Recalled for Instruction Manual Updates
Abbott Laboratories is recalling 22,359 Transferrin in vitro diagnostic kits to update the Instructions for Use (IFU) regarding reagents and specimen handling.
Product
Transferrin is an in vitro diagnostic assay for the quantitative determination of transferrin in human serum or plasma. Antigen in the sample bonds to the specific antibody in the reagent, forming an immune complex. The immune complex causes an increase in light…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1516-2019·2019-07-31
Amneal Recalls Methylergonovine Maleate Tablets Due to Foreign Tablet Presence
Amneal Pharmaceuticals is recalling specific lots of Methylergonovine Maleate tablets because a Promethazine tablet was found in a bottle.
Product
Methylergonovine Maleate USP 0.2 mg Tablets a) 12 count (NDC 69238-1605-02) and b) 28 count bottles (NDC 69238-1605-08)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1497-2019·2019-07-31
Pharma-Natural Recalls GENCONTUSS Cough Syrup Due to Manufacturing Violations
Pharma-Natural Inc. is recalling 3,000 bottles of GENCONTUSS cough syrup because it was manufactured with current good manufacturing practice violations.
Product
GENCONTUSS — GENCONTUSS (CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1506-2019·2019-07-31
Pharma-Natural Recalls NEOGEN-D Cough Syrup Due to Manufacturing Violations
Pharma-Natural Inc. is recalling 2,052 bottles of NEOGEN-D cough syrup because the product was manufactured with current good manufacturing practice violations, including a lack of process and cleaning validation.
Product
NEOGEN-D (Dextromethorphan HBr, 30 mg; Guaifenesin, 200 mg; Phenylephrine HCl, 7.5 mg) in each 5 mL tsp, Raspberry Flavor, 16 fl oz (473 mL) bottle, Manufactured in the USA for Kramer Novis, San Juan, PR 00917, NDC 52083-699-16.
Category
Drug
Distribution
Distributed nationwide