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.

40876–40900 of 79631

SevereFDA (Drugs)·D-0929-2018·2018-07-25
Avella Recalls CeFAZolin Bags Due to Potential Leakage and Sterility Concerns
Avella of Deer Valley, Inc. is recalling 2,500 bags of ceFAZolin 2 gm in NS 100mL due to potential bag leakage that compromises sterility.
Product
ceFAZolin 2 gm in NS 100mL. ceFAZolin Sodium (USP) 2gm, 0.9% Sodium Chloride (USP) 100mL. Volume 110 mL. Single dose bag. Avella of Houston 9265 Kirby Dr., Houston, TX 77054 NDC: 42852-604-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2516-2018·2018-07-25
Medtronic Tri-Staple 2.0 Curved Tip Reloads Recalled for Missing Sled Component
Medtronic is recalling Tri-Staple 2.0 Curved Tip Intelligent Reloads because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Product
Tri-Staple 2.0 Curved Tip Intelligent Reload for use with Signia stapling system , Item Code EGIA30CTAV
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0937-2018·2018-07-25
Avella Recalls Midazolam Bags Due to Potential Leakage and Sterility Concerns
Avella of Deer Valley, Inc. is recalling 1,860 bags of Midazolam 1 mg/mL due to potential bag leakage and lack of assurance of sterility.
Product
Midazolam 1 mg/mL (Midazolam HCL (USP) 100 mg, Sodium Chloride, USP QS 100 mL) Volume: 100 mL. Single dose bag. Avella of Houston, 9265 Kirby Dr., Houston TX 77054. NDC 4252-401-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2503-2018·2018-07-25
Endo GIA 45 mm Articulating Medium/Thick Reload Recalled for Missing Sled Component
COVIDIEN MEDTRONIC is recalling Endo GIA 45 mm Articulating Medium/Thick Reloads because a missing sled component may prevent staple formation, leading to bleeding or leakage.
Product
Endo GIA 45 mm Articulating Medium/Thick Reload with Tri-Staple Technology, Item Code EGIA45AMT
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2510-2018·2018-07-25
Medtronic Endo GIA Reloads Recalled for Missing Sled Component
Medtronic is recalling specific Endo GIA 45 mm Extra Thick Black Articulating Reloads because a missing sled component may prevent staple formation, potentially leading to bleeding or leakage.
Product
Endo GIA 45 mm Extra Thick Black Articulating Reload with Tri-Staple Technology, Item Code EGIA45AXT
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0957-2018·2018-07-25
Avella Recalls Midazolam Syringes Due to Sterility Assurance Concerns
Avella of Deer Valley, Inc. is recalling 110 syringes of Midazolam 1 mg/mL due to a lack of assurance of sterility and potential bag leakage.
Product
Midazolam 1 mg/mL (Midazolam HCL (USP) 55 mg, 0.9% Sodium Chloride, (USP) QS 55 mL) Volume: 55mL. Single dose syringe. Advanced Pharma, 9265 Kirby Dr., Houston TX 77054. NDC 15082-401-76
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0958-2018·2018-07-25
Avella Recalls NORepiNEPHrine 16 Bags Due to Sterility Concerns
Avella of Deer Valley, Inc. is recalling 520 bags of NORepiNEPHrine 16 injection due to potential bag leakage and lack of assurance of sterility.
Product
NORepiNEPHrine 16 (NORepiNEPHrine Bitartrate (USP) 16 mg, 5% Dextrose Inj. (USP) 250 mL. Volume: 266 mL. Single dose bag. Avella of Houston, 9265 Kirby Dr. Houston, TX 77054. NDC 42852-834-25
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0953-2018·2018-07-25
Avella Recalls Morphine Bags Due to Potential Leakage and Sterility Concerns
Avella of Deer Valley is recalling 130 bags of Morphine 1 mg/mL due to potential bag leakage and lack of assurance of sterility.
Product
MORphine 1 mg/mL (Morphine Sulfate, USP 250mg, 0.9% Sodium Chloride, USP 250 mL). Volume 255 mL. Single dose bag. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054. NDC 42852-241-25
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2497-2018·2018-07-25
RayStation Software Recalled for Potential Radiation Overdose Risk
RaySearch Laboratories is recalling RayStation treatment planning software versions 4.5 through 8A because a calculation error could lead to significant radiation overdosage during therapy.
Product
RayStation stand-alone software treatment planning system, RayStation 4.5, RayStation 4.7, RayStation 4.9 (RayPlan 1), RayStation 5, RayStation 6 (RayPlan 2), RayStation 7 (RayPlan 7) and RayStation 8A (RayPlan 8A) Product Usage: RayStation is a software system designed for…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0955-2018·2018-07-25
Avella Recalls Midazolam Syringes Due to Potential Sterility Issues
Avella of Deer Valley, Inc. is recalling specific lots of Midazolam 1 mg/mL syringes due to a lack of assurance of sterility and potential bag leakage.
Product
Midazolam 1 mg/mL (Midazolam HCL USP 30 mg, 0.9% Sodium Chloride, USP QS 30 mL) Volume: 30 mL. Single dose syringe. For: Methodist Willowbrook Hospital, By: Advanced Pharma, 9265 Kirby Dr., Houston TX 77054. NDC 15082-401-63
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2505-2018·2018-07-25
Medtronic Endo GIA Reloads Recalled for Missing Sled Component
Medtronic is recalling specific Endo GIA 60 mm reloads because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Product
Endo GIA 60 mm Extra Thick Black Articulating Reload with Tri-Staple Technology, Item Code EGIA60AXT
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0956-2018·2018-07-25
Avella Recalls Midazolam Bags Due to Potential Leakage and Sterility Concerns
Avella of Deer Valley is recalling 220 bags of Midazolam 0.5mg/mL due to potential bag leakage and lack of assurance of sterility.
Product
Midazolam 0.5mg/mL (Midazolam HCL (USP) 50 mg, 0.9% Sodium Chloride, USP QS 100 mL) Volume: 100 mL. Single dose bag. For: Coral Gables Hospital, By: Advanced Pharma, 9265 Kirby Dr., Houston TX 77054. NDC 15082-408-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0935-2018·2018-07-25
Avella Recalls Hydromorphone Syringes Due to Sterility Assurance Concerns
Avella of Deer Valley, Inc. is recalling 275 single-dose hydromorphone syringes nationwide due to a lack of assurance of sterility caused by potential bag leakage.
Product
HYDROmorphone 1 mg/mL (HYDROmorphone HCL (USP) 50 mg, 0.9% Sodium Chloride (USP) QS 50 mL) Volume: 50mL. Single dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX. NDC 42852-222-65
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2470-2018·2018-07-25
Ion Beam Applications Recalls Proteus 235 Nozzles Due to Crushing Risk
Ion Beam Applications is recalling 14 Proteus 235 nozzles because they may allow gantry rotation or proton irradiation when accessories are not correctly positioned, posing a risk of crushing or mistreatment.
Product
Proteus 235, Universal Nozzle with snout 300x400; PBS dedicated nozzle with snout XL Product Usage: Device is designed to produce and deliver proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation. The PTS…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0928-2018·2018-07-25
Avella Recalls Ropivacaine Pumps Due to Potential Sterility Compromise
Avella of Deer Valley is recalling 40 Ropivacaine OnQ pumps due to potential bag leakage that compromises sterility.
Product
0.2% ROPivacaine - OnQ Pump, (ROPivacaine HCL (USP) 1100mg, 0.9% Sodium Chloride (USP) QS 550 ml, single dose pump. For: Vidant Medical Center, By: Avella of Houston, 9265 Kirby Dr., Houston, TX 77056. NDC: 42852-661-02
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0950-2018·2018-07-25
Avella Recalls Hydromorphone Injection Bags Due to Sterility Concerns
Avella of Deer Valley, Inc. is recalling 660 bags of Hydromorphone injection due to potential leakage that compromises sterility.
Product
HYDROmorphone 0.2mg/mL. (Hydromorphone HCL (USP) 20 mg, 0.9% Sodium Chloride (USP) QS 100 mL) Volume: 100mL. Single dose bag. Advanced Pharma, 9265 Kirby Dr., Houston,077054 TX. NDC 15082-221-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0931-2018·2018-07-25
Avella Recalls Epinephrine Bags Due to Potential Leakage and Sterility Concerns
Avella of Deer Valley is recalling 420 bags of Epinephrine 4 mg in 5% Dextrose due to potential leakage that compromises sterility.
Product
EPINEPHrine (USP) 4 mg, 5% Dextrose For Inj. (USP) 250 mL Volume: 254 mL single dose bag. For: Peninsular Regional Medical Center. By: Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054. NDC 15082-855-25.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0951-2018·2018-07-25
Avella Recalls Magnesium Sulfate Bags Due to Sterility Concerns
Avella of Deer Valley, Inc. is recalling 25 bags of Magnesium Sulfate in Sodium Chloride due to potential leakage and lack of sterility assurance.
Product
MAGnesium 1gm in NS 100 mL (MAGnesium SULfate (USP) 1 gm, 0.9% Sodium Chloride (USP) 100 mL). Volume: 102 mL. Single dose bag. For: Salt Lake Regional Med Ctr By: Avella of Houston, 9256 Kirby Dr., Houston, TX 77054. NDC: 42852-906-10
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2444-2018·2018-07-25
NewDeal ADVANSYS TTC Medical Devices Recalled for Infection Risk
NewDeal SA is recalling ADVANSYS TTC medical devices because they may cause superficial or deep infections requiring antibiotic treatment or device removal.
Product
ADVANSYS TTC, Model Numbers: 181011S, 181012S, 181013S, 181014S, 181001S, 181002S, 181003S & 181004S
Category
Medical Device
Distribution
19 states
SevereFDA (Drugs)·D-0963-2018·2018-07-25
Avella Recalls Ephedrine Sulfate Syringes Due to Sterility Concerns
Avella of Deer Valley is recalling 10,500 ephedrine sulfate syringes nationwide due to potential bag leakage and lack of sterility assurance.
Product
ePHEDrine Sulfate, USP 25 mg in 0.9% Sodium Chloride, USP QS 5mL. Volume 5 mL Single dose syringe. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054 NDC 42852-805-67
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0932-2018·2018-07-25
Avella Recalls Epinephrine Bags Due to Potential Leakage and Sterility Concerns
Avella of Deer Valley, Inc. is recalling 700 bags of Epinephrine (USP) 4 mg due to potential leakage that compromises sterility.
Product
EPINEPHrine (USP) 4 mg, 0.9% Sodium Chloride (USP) 250 mL Volume: 254 mL single dose bag. Avella of Houston, 9265 Kirby Dr., Houston, TX 77054. NDC 42852-823-25.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0941-2018·2018-07-25
Avella Recalls Vancomycin Bags Due to Potential Leakage
Avella of Deer Valley is recalling 1,352 bags of Vancomycin 1.25gm in D5W 250 mL due to potential leakage that compromises sterility.
Product
Vancomycin 1.25gm in D5W 250 mL. ( Vancomycin HCL (USP) 1.25 gm, 5% Dextrose Inj. (USP) 250 mL) Volume: 262 mL. Single dose bag. Avella Specialty Pharmacy, 24416N 19th Avenue, Phoenix, AZ 85085. NDC 42852-617-25
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0946-2018·2018-07-25
Avella Recalls Fentanyl and Ropivacaine Cassettes Due to Sterility Concerns
Avella of Deer Valley is recalling 100 fentanyl and ropivacaine cassettes due to potential bag leakage and lack of sterility assurance.
Product
fentaNYL 2 mcg/mL, 0.125% ROPivacaine, Fentanyl Citrate, USP 300 mcg, Ropivacaine HCL PF, USP 187.5 mg, 0.9% Sodium Chloride, USP QS 150 mL. Volume: 150 mL. Single dose cassette For: Methodist Dallas Medical Center. By: Advanced Pharma, 9265 Kirby Dr., Houston, TX 77054. NDC…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2513-2018·2018-07-25
Medtronic Tri-Staple 2.0 Reloads Recalled for Missing Sled Component
Medtronic is recalling Tri-Staple 2.0 Intelligent Reloads because a missing sled component may prevent staple formation, leading to bleeding or leakage.
Product
Tri-Staple 2.0 Intelligent Reload for use with Signia stapling system 30 mm Medium/Thick, Item Code SIG30AMT
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2504-2018·2018-07-25
Medtronic Endo GIA Reloads Recalled for Missing Sled Component
Medtronic is recalling specific Endo GIA 60 mm reloads because a missing sled component may prevent staple formation, potentially causing bleeding or leakage.
Product
Endo GIA 60 mm Articulating Medium/Thick Reload with Tri-StapleTechnology, Item Code EGIA60AMT
Category
Medical Device
Distribution
Distributed nationwide