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.

35451–35475 of 79559

HighFDA (Devices)·Z-2053-2019·2019-07-31
MOOG Curlin Infusion Administration Set Recalled for Filter Leaks
Zevex Incorporated is recalling MOOG Curlin Infusion Administration Sets because they leaked at the filter. The affected sterile sets were distributed to six US states.
Product
MOOG Curlin Infusion Administration Set, REF 340-4130, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter, packaged 20 sets/carton, sterile. Product Usage: Administration set to be used with the Moog Curlin Infusion Pump. The pump can be used for…
Category
Medical Device
Distribution
6 states
HighFDA (Drugs)·D-1511-2019·2019-07-31
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
HighFDA (Devices)·Z-2041-2019·2019-07-31
Cardinal Health Recalls Monoject Hypodermic Needles Due to Sterility Concerns
Cardinal Health is recalling Monoject Standard Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.
Product
Monoject Standard Hypodermic Needle, 27 G x 1-1/4" Item code: 8881200508
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1595-2019·2019-07-31
FoodScience Recalls Mislabeled Omega 3 Dietary Supplement
FoodScience Corporation is recalling 256 bottles of DaVinci Laboratories Omega 3-1,000 dietary supplements due to mislabeling and an undeclared allergen.
Product
DaVinci Laboratories of Vermont Omega 3-1,000 in a white bottle labeled as Dim Plex, 60 count UPC Code 026664273161
Category
Food
Distribution
18 states
HighFDA (Devices)·Z-2003-2019·2019-07-31
Terumo Sur-vet Needle Recall Due to Potential Loss of Package Integrity
Terumo Medical Corporation is recalling 563,000 Sur-vet Needles because a potential loss of package integrity may compromise the sterility of the product.
Product
Terumo Sur-vet Needle, 25G x 5/8", Product Code 100280
Category
Medical Device
Distribution
12 states
HighFDA (Devices)·Z-1996-2019·2019-07-31
Stanley Healthcare Recalls Arial 54315 Network Manager Due to Outages
Stanley Healthcare is recalling 137 Arial 54315 Network Managers because they caused outages in the Arial nurse call system.
Product
STANLEY Healthcare Arial 54315 Network Manager
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1599-2019·2019-07-31
Flowers Foods Recalls Dinner Rolls Due to Potential Plastic Contamination
Flowers Foods is recalling Laura Lynn and Wonder dinner rolls because they may contain small pieces of hard plastic introduced during production.
Product
Dinner Rolls sold under the brand names of Laura Lynn UPC 86854 06669 0 & Wonder 12 CT UPC 72250 07421 6 24 CT UPC 72250 01169 3
Category
Food
Distribution
18 states
HighFDA (Devices)·Z-2004-2019·2019-07-31
Terumo 18G Needles Recalled for Potential Loss of Package Integrity
Terumo Medical Corporation is recalling 810,000 18G needles due to a potential loss of package integrity that may compromise sterility.
Product
Terumo Needle, 18G x 1", Product Code NN1825R
Category
Medical Device
Distribution
12 states
HighFDA (Devices)·Z-2009-2019·2019-07-31
Philips BrightView SPECT Recalled for Uncommanded Handcontroller Motion
Philips Medical Systems is recalling 696 BrightView SPECT units because the handcontroller may move spontaneously or continue moving after buttons are released.
Product
BrightView SPECT, Model Number 882480
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2022-2019·2019-07-31
Siemens AXIOM Artis dBA X-ray Generator Recall for Power Supply Issue
Siemens is recalling 85 AXIOM Artis dBA units because a power supply tolerance issue may cause the X-ray generator to fail during procedures.
Product
AXIOM Artis dBA, Model Number 7555357
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2038-2019·2019-07-31
Cardinal Health Recalls Monoject Hypodermic Needles Due to Sterility Barrier Defect
Cardinal Health 200, LLC is recalling specific lots of Monoject Standard Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.
Product
Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code: 8881200037
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2050-2019·2019-07-31
Cardinal Health Recalls Monoject Blunt Cannula Due to Sterility Barrier Defect
Cardinal Health 200, LLC is recalling Monoject Blunt Cannulas due to a manufacturing defect that could compromise the product's sterility barrier.
Product
Monoject Blunt Cannula, 19 G x 1-1/2" (1.067 mm x 3.8 cm) Item code: 8881202355
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1514-2019·2019-07-31
Baxter Recalls Sodium Chloride Injection Due to Sterility Concerns
Baxter Healthcare is recalling 139,680 containers of 0.9% Sodium Chloride Injection due to a lack of assurance of sterility and potential for bags to leak.
Product
SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1581-2019·2019-07-31
Lupin Recalls Lisinopril and Hydrochlorothiazide Tablets Due to Foreign Object
Lupin Pharmaceuticals is recalling 11,832 bottles of Lisinopril and Hydrochlorothiazide tablets because a foreign tablet was found in the product.
Product
LISINOPRIL AND HYDROCHLOROTHIAZIDE — LISINOPRIL AND HYDROCHLOROTHIAZIDE (LISINOPRIL AND HYDROCHLOROTHIAZIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1597-2019·2019-07-31
Flowers Bratwurst Buns Recalled for Potential Hard Plastic Contamination
Flowers Foods is recalling Flowers Bratwurst Buns 12 CT because they may contain small pieces of hard plastic introduced during production.
Product
Flowers Bratwurst Buns 12 CT UPC 7 22500 40792
Category
Food
Distribution
18 states
HighFDA (Food)·F-1598-2019·2019-07-31
Publix Brown and Serve Rolls Recalled for Potential Plastic Contamination
Flowers Foods is recalling Publix 12 CT Brown & Serve Rolls due to the potential presence of small pieces of hard plastic introduced during production.
Product
Publix 12 CT Brown & Serve Rolls 12 CT UPC 41415 31190 9
Category
Food
Distribution
18 states
HighFDA (Devices)·Z-2057-2019·2019-07-31
CooperSurgical LEEP Precision System Foot Pedal Function Defect Recall
CooperSurgical is recalling LEEP Precision Integrated Systems because the foot pedal may fail to operate the cut, coagulate, or blend functions.
Product
LEEP Precision Integrated System 120V & LEEP Precision Generator, Model Nos. LP-10-120 & LP-20-120
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2047-2019·2019-07-31
Cardinal Health Recalls Monoject 201 Vet Pak Hypodermic Needles
Cardinal Health is recalling Monoject 201 Vet Pak Hypodermic Needles due to a manufacturing defect that could compromise the sterility barrier.
Product
Monoject" 201 Vet Pak Hypodermic Needle, 16 ga x 1-1/2 Item code: 8881201654
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1512-2019·2019-07-31
FDA Recalls Temozolomide Capsules Due to Cross-Contamination Risk
Deva Holding AS is recalling Temozolomide Capsules because manufacturing deviations allowed for possible cross-contamination with beta-lactam products.
Product
TEMOZOLOMIDE — TEMOZOLOMIDE (TEMOZOLOMIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-1600-2019·2019-07-31
Flowers Enriched Rolls Recalled for Potential Hard Plastic Contamination
Flowers Foods is recalling 1,467 packages of Flowers Enriched Rolls because they may contain small pieces of hard plastic introduced during production.
Product
Flowers Enriched Rolls UPC 70210 00686 4
Category
Food
Distribution
18 states
HighFDA (Devices)·Z-2046-2019·2019-07-31
Cardinal Health Recalls Monoject 201 Vet Pak Hypodermic Needles
Cardinal Health is recalling specific lots of Monoject 201 Vet Pak Hypodermic Needles due to a manufacturing defect that could compromise the product's sterility barrier.
Product
Monoject 201 Vet Pak Hypodermic Needle, 18 ga x 1-1/2 Item code: 8881201548
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2049-2019·2019-07-31
Cardinal Health Recalls Monoject Blunt Cannula Due to Sterility Barrier Defect
Cardinal Health 200, LLC is recalling Monoject Blunt Cannulas due to a manufacturing defect that could compromise the product's sterility barrier.
Product
Monoject Blunt Cannula, 16 G x 1-1/2" (1.651 mm x 3.8 cm) Item code: 8881202322
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1607-2019·2019-07-31
Krystal Sandwich Slider Buns Recalled for Potential Plastic Contamination
Flowers Foods is recalling Krystal 24 Sheet Sandwich Slider Buns because they may contain small pieces of hard plastic introduced during production.
Product
Krystal 24 Sheet Sandwich Slider Buns
Category
Food
Distribution
18 states
HighFDA (Devices)·Z-2051-2019·2019-07-31
Cardinal Health Recalls Monoject Blunt Cannula Due to Sterility Barrier Defect
Cardinal Health 200, LLC is recalling Monoject Blunt Cannula, 20 G x 1-1/2" (Item code: 8881202363), because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.
Product
Monoject Blunt Cannula, 20 G x 1-1/2" (0.902 mm x 3.8 cm) Item code: 8881202363
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2054-2019·2019-07-31
MOOG Curlin Infusion Administration Sets Recalled for Filter Leaks
Zevex Incorporated is recalling specific lots of MOOG Curlin Infusion Administration Sets because they leaked at the filter.
Product
MOOG Curlin Infusion Administration Set, REF 340-4130-V, Non-DEHP Tubing with Non-Vented Bag Spike and Vented 0.2 Micron Filter with add-on check valve, packaged 20 sets/carton, sterile. The firm name on the label is ZEVEX, Inc., Salt Lake City, UT.
Category
Medical Device
Distribution
6 states