State

Kansas product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46676–46700 of 79639

HighFDA (Devices)·Z-2134-2017·2017-05-31
Cardinal Health Recalls Jackson-Pratt Hemaduct Silicone Round Drains
Cardinal Health is recalling specific lots of Jackson-Pratt Hemaduct Silicone Round Drains because the product seal may be compromised, potentially increasing the risk of infection.
Product
Jackson-Pratt Hemaduct Silicone Round Drain, 10FR W/10FR Trocar. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems are sterile single use devices. The wound drainage system consist of a wound drain and a fluid collection reservoir. The wound drain…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2140-2017·2017-05-31
Cardinal Health Recalls Jackson-Pratt Wound Drains Due to Sterility Concerns
Cardinal Health is recalling specific lots of Jackson-Pratt PVC Round Drains because the product seal may be compromised, potentially increasing the risk of infection.
Product
Jackson-Pratt PVC Round Drain, 10FR W/Trocar. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems are sterile single use devices. The wound drainage system consist of a wound drain and a fluid collection reservoir. The wound drain is a radio-opaque…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2122-2017·2017-05-31
Cardiovascular Systems Recalls Orbital Atherectomy System Saline Infusion Pumps
Cardiovascular Systems Inc. is recalling 1,396 Saline Infusion Pumps that may switch to stand-by during use, requiring a reset to continue treatment.
Product
CSI, Orbital Atherectomy System (OAS) Saline Infusion Pump, Rx only, Part Number: 7-10014, Model Number: SIP-3000.
Category
Medical Device
Distribution
44 states
HighFDA (Devices)·Z-2143-2017·2017-05-31
Cardinal Health Recalls Jackson-Pratt Silicone Flat Drains Due to Sterility Concerns
Cardinal Health 200, LLC is recalling Jackson-Pratt Silicone Flat Drains because the product seal may be compromised, potentially compromising sterility and increasing the risk of infection.
Product
Jackson-Pratt Silicone Flat Drain, 7mm, Full Ducts. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems are sterile single use devices. The wound drainage system consist of a wound drain and a fluid collection reservoir. The wound drain is a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2164-2017·2017-05-31
Datascope Recalls Intra-Aortic Balloon Catheters Due to Tip Seal Leak Failures
Datascope is voluntarily removing 996 units of SENSATION PLUS Intra-Aortic Balloon Catheters due to internal pressure testing failures related to tip seal leaks.
Product
SENSATION PLUS¿ 8Fr. 50cc Intra-Aortic Balloon Catheter with Insertion Kit & STATLOCK¿ Product Code/Part Number: 0684-00-0576-01U is a cardiac assist device which support the heart's left ventricle by increasing coronary perfusion and reducing the work of the left ventricle.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2146-2017·2017-05-31
Cardinal Health Recalls Jackson-Pratt Silicone Round Drains Due to Seal Compromise
Cardinal Health 200, LLC is recalling Jackson-Pratt Silicone Round Drains because the product seal may be compromised, potentially compromising sterility and increasing infection risk.
Product
Jackson-Pratt Silicone Round Drain, 10FR. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems are sterile single use devices. The wound drainage system consist of a wound drain and a fluid collection reservoir. The wound drain is a radio-opaque section…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2157-2017·2017-05-31
Beckman Coulter UniCel DxH 800 Recalled for Potential Data Errors
Beckman Coulter is recalling UniCel DxH 800 systems because a software issue may cause erroneous white blood cell differential results.
Product
UniCel DxH 800 Coulter Cellular Analysis System, Catalog No. 629029, B24465, B24802, B66445, B68304, B63322.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2158-2017·2017-05-31
Beckman Coulter UniCel DxH 600 Recall for Erroneous WBC Differential Results
Beckman Coulter is recalling UniCel DxH 600 systems due to a software issue that may cause erroneous white blood cell differential results.
Product
UniCel DxH 600 Coulter Cellular Analysis System, Catalog No. B23858.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2243-2017·2017-05-31
Rich Products Recalls Pizza Dough Balls Due to E. coli 0121 Risk
Rich Products Corp is recalling 7 oz pizza dough balls because the flour used may be contaminated with E. coli 0121.
Product
7 OZ PIZZA DOUGH BALL, PRODUCT CODE 11267, UPC 0 00 49800 1267 4, NET CASE WT 12.9 KG (28 LB 7 OZ), UNIT NET WT: 198 G (7 OZ), COUNT: 65 --- PROCESSED IN CANADA, DIST. BY RICH PRODUCTS CORPORATION, BUFFALO, N.Y. 14213 U.S.A.
Category
Food
Distribution
34 states
HighFDA (Devices)·Z-2147-2017·2017-05-31
Cardinal Health Recalls Jackson-Pratt Silicone Round Drains Due to Sterility Concerns
Cardinal Health 200, LLC is recalling specific lots of Jackson-Pratt Silicone Round Drains because the product seal may be compromised, potentially increasing the risk of infection.
Product
Jackson-Pratt Silicone Round Drain, 15FR. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems are sterile single use devices. The wound drainage system consist of a wound drain and a fluid collection reservoir. The wound drain is a radio-opaque section…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2117-2017·2017-05-31
Medtronic Recalls MRI-Conditional Cardiac Resynchronization Therapy Devices
Medtronic is recalling specific MRI-conditional CRT-D devices due to an unexpected transient mode switch behavior detected during systems testing.
Product
Amplia MRI Quad CRT-0 SureScan Claria MRI Quad CRT-D SureScan Compia MRI Quad CRT-D SureScan
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2139-2017·2017-05-31
Cardinal Health Recalls Jackson-Pratt Hemaduct Silicone Round Drains
Cardinal Health 200, LLC is recalling Jackson-Pratt Hemaduct Silicone Round Drains because the product seal may be compromised, potentially compromising sterility and increasing infection risk.
Product
Jackson-Pratt Hemaduct Silicone Round Drain, 10FR W/Trocar. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems are sterile single use devices. The wound drainage system consist of a wound drain and a fluid collection reservoir. The wound drain is a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-2244-2017·2017-05-31
Rich Products Recalls Artisan Crust Pizza Dough Due to E. coli Risk
Rich Products Corp is recalling Artisan Crust Pizza Dough because the flour used may be contaminated with E. coli O121.
Product
ARTISAN CRUST PIZZA DOUGH 24/18, PRODUCT CODE 11413, UPC 1 00 49800 11413 2, NET CASE WT: 27 LB (12.2 KG), UNIT NET WT: 18 OZ (1 LB 2 OZ) (510G), COUNT: 24 --- PROCESSED IN CANADA DIST. BY RICH PRODUCTS CORPORATION, BUFFALO, N.Y. 14213 U.S.A.
Category
Food
Distribution
34 states
HighFDA (Devices)·Z-2131-2017·2017-05-31
Cardinal Health Recalls Jackson-Pratt Hemaduct Cardiothoracic Silicone Round Drains
Cardinal Health is recalling specific lots of Jackson-Pratt Hemaduct Cardiothoracic Silicone Round Drains because the product seal may be compromised, potentially compromising sterility and increasing infection risk.
Product
Jackson-Pratt Hemaduct Cardiothoracic Silicone Round Drain,19FR. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems are sterile single use devices. The wound drainage system consist of a wound drain and a fluid collection reservoir. The wound drain…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·17V353000·2017-05-31
Terex Advance Recalls 2017 Front Discharge Concrete Mixers Due to Tank Welds
Terex Advance is recalling 2017 Front Discharge Concrete Mixers because welds on the 250-gallon water tank filler neck may fail, posing an injury risk.
Product
TEREX ADVANCE — TEREX ADVANCE FRONT DISCHARGE CONCRETE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2145-2017·2017-05-31
Cardinal Health Recalls Jackson-Pratt Silicone Round Drains Due to Seal Compromise
Cardinal Health 200, LLC is recalling Jackson-Pratt Silicone Round Drains because the product seal may be compromised, potentially compromising sterility and increasing infection risk.
Product
Jackson-Pratt Silicone Round Drain, 7FR. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems are sterile single use devices. The wound drainage system consist of a wound drain and a fluid collection reservoir. The wound drain is a radio-opaque section…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2133-2017·2017-05-31
Cardinal Health Recalls Jackson-Pratt Hemaduct Silicone Flat Drains
Cardinal Health 200, LLC is recalling Jackson-Pratt Hemaduct Silicone Flat Drains because the product seal may be compromised, potentially compromising sterility and increasing infection risk.
Product
Jackson-Pratt Hemaduct Silicone Flat Drain, 10mm, Full Ducts W/15FR Trocar. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems are sterile single use devices. The wound drainage system consist of a wound drain and a fluid collection reservoir. The…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2141-2017·2017-05-31
Cardinal Health Recalls Jackson-Pratt Silicone Flat Drains Due to Sterility Concerns
Cardinal Health is recalling specific lots of Jackson-Pratt Silicone Flat Drains because the product seal may be compromised, potentially increasing the risk of infection.
Product
Jackson-Pratt Silicone Flat Drain, 7mm, 3/4 Ducts. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems are sterile single use devices. The wound drainage system consist of a wound drain and a fluid collection reservoir. The wound drain is a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2160-2017·2017-05-31
Stryker Recalls Hoffmann LRF Safety Clips Due to Loosening Risk
Stryker is recalling Hoffmann LRF Safety Clips because they may loosen from the Quick Release mechanism on Transport Struts.
Product
Hoffmann LRF Safety Clip (Bone Transport Strut), 14 x 12 x 5 mm, REF 4933-0-401, NDC (01)07613327131475(10)V07241 Product Usage: Intended for fixation of fractures, joint contractures, fusions, limb lengthening, deformity correction, and bone and soft tissue reconstruction…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2148-2017·2017-05-31
Cardinal Health Recalls Jackson-Pratt Silicone Round Drains Due to Sterility Concerns
Cardinal Health 200, LLC is recalling specific lots of Jackson-Pratt Silicone Round Drains because the product seal may be compromised, potentially increasing the risk of infection.
Product
Jackson-Pratt Silicone Round Drain, 19FR. Sterile, Rx Only. For Single Use Only. Jackson-Pratt Wound Drainage Systems are sterile single use devices. The wound drainage system consist of a wound drain and a fluid collection reservoir. The wound drain is a radio-opaque section…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0824-2017·2017-05-31
Advanced Pharma Recalls Diltiazem HCl Due to Latex Labeling Defect
Advanced Pharma Inc. is recalling all Diltiazem HCl products because they may contain latex but lack proper labeling.
Product
Diltiazem HCl all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0801-2017·2017-05-31
Advanced Pharma Recalls Ropi Epi Clon Injection Due to Latex Labeling
Advanced Pharma Inc. is recalling Ropi/ Epi/ Clon PeriCapsular injection because the product may contain latex and lacks appropriate labeling.
Product
Ropi/ Epi/ Clon PeriCapsular injection all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0866-2017·2017-05-31
Gentell Recalls Moisture Barrier Cream Due to Manufacturing Deviations
Gentell, Inc. is recalling 65 gallons of Shield and Protect Moisture Barrier Cream because it may not meet cGMP requirements.
Product
Shield and Protect Moisture Barrier Cream, 1.1% Clotrimazole, Net Weight 4 oz - 115 g Anti-Fungal, Gentell, Inc., Bristol, PA NDC 61554-232-40
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0846-2017·2017-05-31
Advanced Pharma Recalls Dexmedetomidine HCl Due to Latex Labeling
Advanced Pharma Inc. is recalling all lots of Dexmedetomidine HCl because the product may contain synthetic or natural latex, which is not currently labeled.
Product
Dexmedetomidine HCl all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0821-2017·2017-05-31
Advanced Pharma Recalls Oxytocin Due to Potential Latex Content
Advanced Pharma Inc. is recalling all Oxytocin products due to a labeling issue regarding potential synthetic or natural latex content.
Product
Oxytocin all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
Category
Drug
Distribution
Distributed nationwide