State

Kansas product recalls

20,322 recalls have nationwide distribution and so reach Kansas. 0 additional recalls listed Kansas specifically in their distribution scope.

About recalls in Kansas

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Kansas consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

11926–11950 of 20322

SevereFDA (Devices)·Z-2368-2023·2023-08-23
Dialysis Catheter Recalled Due to Excessive Lubricant Causing Center Lumen Obstruction
Covidien is recalling MAHURKAR dialysis catheters due to excessive silicone-based lubricant coating the center lumen tip, which may cause partial or complete obstruction, delaying treatment or causing thrombosis.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 16 cm, Curved Extensions, IC Tray REF: 8888101002HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2372-2023·2023-08-23
FDA Recalls MAHURKAR Dialysis Catheters Over Obstruction Defect Risk
Covidien's MAHURKAR dialysis catheters are recalled due to excessive lubricant on the catheter tip causing partial or complete obstruction. This risks delaying treatment and may cause blood clots, hemolysis, or embolism.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Straight Extensions, IC Tray REF: 8888102004HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2387-2023·2023-08-23
Dialysis Catheters Recalled by FDA for Tip Obstruction Risk
Covidien is recalling MAHURKAR acute dialysis catheters because the center lumen tip may be occluded by excessive silicone-based lubricant. Obstruction could delay treatment or cause embolism and thrombosis.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 16 cm, Curved Extensions, Kit REF: 8888345611HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2388-2023·2023-08-23
Dialysis Catheter Recall Due to Center Lumen Occlusion
Covidien is recalling MAHURKAR Triple Lumen Acute Dialysis Catheters due to excessive lubricant blocking the center lumen, which may delay dialysis and cause blood clots. The recall affects 6,949 units distributed in the US and worldwide.
Product
MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, Kit" REF: 8888345629
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2377-2023·2023-08-23
Acute Dialysis Catheters Recalled for Catheter Tip Occlusion
Covidien recalls 519 MAHURKAR acute dialysis catheters (Lot 2200400292) due to excessive silicone lubricant coating the catheter tip that may cause partial or full occlusion and treatment delays.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Straight Extensions, PASS Tray REF: 8888104004HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2406-2023·2023-08-23
Alcon Constellation Procedure Pak recalled due to plastic debris risk
Alcon is recalling the Constellation Procedure Pak due to reports of patient injury from plastic debris. The debris can result from over-tightening the device with the included plastic wrench.
Product
Constellation Procedure Pak
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2382-2023·2023-08-23
Mahurkar Dialysis Catheter Center Lumen Occlusion, FDA Class I Recall
Covidien's Mahurkar dialysis catheters are recalled due to center lumen occlusion from excessive silicone lubricant, risking treatment delay and serious vascular complications.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 16 cm, Curved Extensions REF: 8888345512HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2379-2023·2023-08-23
Dialysis Catheters Recalled Due to Excessive Lubricant Causing Obstruction
Covidien is recalling MAHURKAR dialysis catheters that may have excessive lubricant coating the catheter tip, potentially causing dangerous blockages that delay treatment or lead to serious complications.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Straight Extensions, Kit REF: 8888340629HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2385-2023·2023-08-23
Acute Dialysis Catheter Recalled for Potential Lumen Obstruction and Embolism Risk
Covidien is recalling MAHURKAR acute dialysis catheters for excessive silicone lubricant causing lumen obstruction that may delay treatment and lead to hemolysis, embolism, or thrombosis.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 13 cm, Curved Extensions, Kit REF: 8888345603HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2411-2023·2023-08-23
Alcon Custom Pak Intraocular Lens Packages Recalled for Plastic Debris Risk
Alcon Custom Pak intraocular lens packages are recalled due to reports of patient injury during surgical procedures caused by plastic debris from over-tightening with the included plastic wrench.
Product
Alcon Custom Pak
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2408-2023·2023-08-23
Infinity FMS Pak surgical device recalled for plastic debris hazard
Alcon is recalling the Infinity FMS Pak surgical device after reports of patient injuries during procedures caused by plastic debris from over-tightening the included wrench. The recall affects 51,054 units distributed worldwide.
Product
Infinity FMS Pak
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2367-2023·2023-08-23
Covidien MAHURKAR Dialysis Catheter Recalled for Lumen Occlusion Risk
Covidien is recalling dialysis catheters with excessive lubricant in the center lumen, which may cause occlusion, obstruct blood flow, and delay treatment.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 13 cm, Curved Extensions, IC Tray REF:8888101001HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2370-2023·2023-08-23
Dialysis catheter recalled due to potential tip occlusion risk
Covidien is recalling MAHURKAR dialysis catheters that may have excessive lubricant in the catheter tip, potentially causing obstruction. This could delay treatment or cause serious blood complications including thrombosis or embolism.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Curved Extensions, IC Tray REF: 8888101004HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2380-2023·2023-08-23
FDA Recalls Mahurkar Dialysis Catheter for Potential Tip Obstruction Risk
Covidien's Mahurkar acute dialysis catheters may have excessive silicone lubricant causing tip obstruction. This could delay treatment or cause serious complications including blood clots and embolism.
Product
MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter, 24 cm, Straight Extensions, Kit REF: 8888340637
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2410-2023·2023-08-23
Phaco Standalone Tips Recalled Due to Plastic Debris Risk
Alcon is recalling 444,372 units of Phaco Standalone Tips worldwide because the plastic wrench included with the product can generate plastic debris when over-tightened, potentially injuring patients.
Product
Phaco Standalone Tips
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2369-2023·2023-08-23
Dialysis Catheter Recalled Due to Silicone Lubricant Obstruction Risk
Covidien LP is recalling 5,373 MAHURKAR dialysis catheters because excessive silicone lubricant can occlude the catheter lumen, potentially causing treatment delays or blood clotting complications.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, IC Tray REF: 8888101003HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2391-2023·2023-08-23
Dialysis Catheter Recalled for Center Lumen Occlusion Risk
Covidien LP is recalling 3,965 MAHURKAR dialysis catheters due to excessive lubricant causing center lumen occlusion. This may obstruct blood flow or cause hemolysis and blood clots.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Curved Extensions, Kit REF: 8888345637HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2389-2023·2023-08-23
MAHURKAR Dialysis Catheter Recalled for Center Lumen Obstruction Risk
Covidien LP recalled 15,209 MAHURKAR dialysis catheters due to excessive lubricant in the center lumen, which may cause catheter occlusion, reduce blood flow, or lead to hemolysis and blood clots.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, Kit REF: 8888345629HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2373-2023·2023-08-23
Dialysis Catheter Recall Due to Potential Lumen Occlusion
Covidien LP is recalling MAHURKAR dialysis catheters due to excess silicone lubricant that can block the central lumen, potentially delaying treatment or causing serious complications.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 13 cm, Curved Extensions, PASS Tray REF: 8888103001HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2371-2023·2023-08-23
Dialysis Catheters Recalled for Catheter Obstruction from Excessive Silicone Lubricant
Covidien is recalling 1,875 MAHURKAR dialysis catheters with lot numbers 2204000239 and 2227800110 due to excessive silicone lubricant causing catheter obstruction. The obstruction may delay treatment or cause hemolysis and thrombosis.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Straight Extensions, IC Tray REF: 8888102003HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2376-2023·2023-08-23
Mahurkar Dialysis Catheters Recalled for Center Lumen Obstruction
Covidien is recalling 1,099 MAHURKAR dialysis catheters worldwide due to excessive silicone lubricant that can block the center lumen, potentially delaying treatment.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Straight Extensions, PASS Tray REF: 8888104003HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2381-2023·2023-08-23
MAHURKAR Dialysis Catheter Recalled for Excessive Lubricant Causing Occlusion
The MAHURKAR dialysis catheter is recalled because excessive silicone lubricant can obstruct the center lumen, potentially delaying critical dialysis treatment.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 24 cm, Straight Extensions, Kit REF: 8888340637HP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2401-2023·2023-08-23
UroPass Ureteral Access Sheaths Recalled for Dilator Tip Breakage
Olympus is recalling UroPass Ureteral Access Sheaths because dilator tips may break during surgical procedures or while in the package. The recall affects 9,520 units manufactured in 2018 and 2019.
Product
UroPass Ureteral Access Sheaths, 5 pieces/box
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2407-2023·2023-08-23
Centurion FMS Pak Recalled Due to Patient Injury Risk from Plastic Debris
Alcon Research recalls the Centurion FMS Pak following reports of patient injury during procedures. Plastic debris can result from over-tightening with the included plastic wrench.
Product
Centurion FMS Pak
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2414-2023·2023-08-23
FreeStyle Libre 2 Readers may fail to activate new sensors
FreeStyle Libre 2 Readers may display an 'Incompatible Sensor' error when attempting to activate a new sensor after incomplete 14-day wear, potentially preventing new sensor activation and causing delayed glucose monitoring.
Product
FreeStyle Libre 2 Readers, REF: 71951-01 and 71953-01, used with FreeStyle Libre 2 System
Category
Medical Device
Distribution
Distributed nationwide