State

Kentucky product recalls

73,219 recalls have nationwide distribution and so reach Kentucky. 7,195 additional recalls listed Kentucky specifically in their distribution scope.

What the numbers show

Total: 7,195
Critical: 1,409
Severe: 1,707
Most recent: 2026-10-02

Of the 7,195 recalls naming Kentucky we have scored against our rubric, 1,409 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,707 (24%) are Severe.

Which agencies issued them

These figures cover only the 7,195 recalls whose distribution notice names Kentucky specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15526–15550 of 80414

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-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-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-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
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
SevereNHTSA·23T005000·2023-08-23
Yokohama Recalls 504C Tires Due to Sidewall Air Leak Risk
Yokohama is recalling 6,992 specific 504C tires because a defective splice may allow air to leak into the sidewall, potentially causing a crash.
Product
TIRES:SIDEWALL recall
Category
Vehicle
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-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-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-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-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-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-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-2374-2023·2023-08-23
Dialysis Catheter Recall: Center Lumen Occlusion Due to Excessive Lubricant
Covidien LP is recalling MAHURKAR 12 Fr dialysis catheters due to center lumen occlusion from excessive lubricant. The defect may cause treatment delays and serious complications including embolism and thrombosis.
Product
MAHURKAR 12 Fr High Pressure Triple Lumen Acute Dialysis Catheter, 20 cm, Curved Extensions, PASS Tray REF: 8888103002HP
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2390-2023·2023-08-23
Dialysis Catheter Occlusion Recall Due to Excessive Lubricant Coating
Covidien recalls 647 MAHURKAR dialysis catheters due to center lumen occlusion caused by excessive silicone lubricant. The blockage may delay treatment or increase risks of blood clots.
Product
MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter, 24 cm, Curved Extensions, Kit REF: 8888345637
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2409-2023·2023-08-23
Legion FMS Pak Surgical Instruments Recalled for Patient Injury from Plastic Debris
Alcon is recalling Legion FMS Pak surgical instruments due to reports of patient injuries caused by plastic debris generated from over-tightening with the included plastic wrench.
Product
Legion FMS Pak
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2386-2023·2023-08-23
MAHURKAR dialysis catheters recalled for center lumen occlusion risk
Covidien LP recalls MAHURKAR dialysis catheters due to excessive silicone lubricant on the catheter tip, which can obstruct the center lumen. This may delay treatment and cause serious blood complications including embolism and thrombosis.
Product
MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter, 16 cm, Curved Extensions, Kit" REF: 8888345611
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2378-2023·2023-08-23
Dialysis catheter recall: excessive lubricant causes center lumen obstruction
A dialysis catheter product is being recalled due to excessive lubricant coating in the center lumen, which may cause full or partial obstruction. The blockage could delay treatment and increase risk of blood clots and hemolysis.
Product
MAHURKAR 12 Fr Triple Lumen Acute Dialysis Catheter, 20 cm, Straight Extensions, Kit REF: 8888340629
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-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-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-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