State

Kentucky product recalls

72,984 recalls have nationwide distribution and so reach Kentucky. 7,165 additional recalls listed Kentucky specifically in their distribution scope.

What the numbers show

Total: 7,165
Critical: 1,399
Severe: 1,694
Most recent: 2026-09-09

Of the 7,165 recalls naming Kentucky we have scored against our rubric, 1,399 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,694 (24%) are Severe.

Which agencies issued them

These figures cover only the 7,165 recalls whose distribution notice names Kentucky specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5951–5975 of 80149

SevereFDA (Devices)·Z-2167-2025·2025-08-06
Hamilton coaxial breathing circuits may have a crack in blue tubing
Coaxial breathing circuit sets for HAMILTON-C1, T1 and MR1 ventilators are being recalled because the blue tubing that delivers fresh gas may be cracked, which can cause rebreathing of exhaled gases. 2,560 units affected.
Product
Breathing circuit set, coaxial, 1.80 m, with flow sensor and expiratory valve set, REF: 260128, used with HAMILTON-C1, HAMILTON-T1 and HAMILTON-MR1 ventilators.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0332-2025·2025-08-06
Sheehan Brothers spicy chicken sandwiches recalled over undeclared sesame
Sheehan Brothers Vending Spicy Chicken Sandwiches, 6.5 oz, are being recalled because of undeclared sesame. 600 individual units are affected.
Product
Sheehan Brothers Vending Spicy Chicken Sandwich, 6.5 oz (184g), individually wrapped in plastic, UPC: 100000222539
Category
Food
Distribution
3 states
SevereFDA (Devices)·Z-2158-2025·2025-08-06
SafeStar 90 Plus breathing filters show a slow rising CO2 curve
SafeStar 90 Plus bidirectional breathing system filters are being recalled following reports of a slow increase of the CO2 curve when the gas sample is taken from the filter's gas sampling port. 669,838 units affected.
Product
SafeStar 90 Plus Filter. Bidirectionally breathing system filter.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2164-2025·2025-08-06
Automated Impella Controllers may not detect a connected Impella pump
The Automated Impella Controller, used with left heart support blood pumps, is being recalled because of a potential issue with the controller not detecting an Impella pump when it is connected. 11,031 units affected.
Product
Automated Impella Controller (AIC), used in left heart support blood pump, including the following: 1. Impella Controller, Packaged, AU; Product Code: 0042-0000-AU. 2. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 3. Impella Controller, Packaged, EU; Pr
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0334-2025·2025-08-06
Sheehan Brothers pepperoni pizza mini subs recalled over undeclared sesame
Sheehan Brothers Vending Pepperoni Pizza Mini Subs, 4.8 oz, are being recalled because of undeclared sesame. 614 individual units are affected.
Product
Sheehan Brothers Vending Pepperoni Pizza Mini Sub, 4.8 oz (136g), in a brown paper boat and individually wrapped in plastic, UPC: 100000222584
Category
Food
Distribution
3 states
SevereFDA (Food)·H-0333-2025·2025-08-06
Sheehan Brothers Italian mini subs recalled over undeclared sesame
Sheehan Brothers Vending Italian Mini Subs, 6.1 oz, are being recalled because of undeclared sesame. 696 individual units are affected.
Product
Sheehan Brothers Vending Italian Mini Sub, 6.1 oz (174g), in a brown paper boat and individually wrapped in plastic, UPC: 100000952412
Category
Food
Distribution
3 states
SevereFDA (Devices)·Z-2159-2025·2025-08-06
SafeStar 55 Plus breathing filters show a slow rising CO2 curve
SafeStar 55 Plus bidirectional breathing system filters are being recalled following reports of a slow increase of the CO2 curve when the gas sample is taken from the filter's port. 9,885,139 units affected.
Product
SafeStar 55 Plus Filter. Bidirectionally breathing system filter.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2160-2025·2025-08-06
HME TwinStar HEPA Plus filters show a slow rising CO2 curve
HME TwinStar HEPA Plus bidirectional breathing system filters are being recalled following reports of a slow increase of the CO2 curve when the gas sample is taken from the filter's port. 1,019,782 units affected.
Product
HME TwinStar HEPA Plus Filter. Bidirectionally breathing system filter.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0331-2025·2025-08-06
Sheehan Brothers vending cheeseburgers recalled over undeclared sesame
Sheehan Brothers Vending Cheeseburgers, 4.7 oz, are being recalled because of undeclared sesame. 824 individual units are affected.
Product
Sheehan Brothers Vending Cheeseburger, 4.7 oz (132g), individually wrapped in plastic, UPC: 100000952375
Category
Food
Distribution
3 states
SevereFDA (Food)·H-0335-2025·2025-08-06
Sheehan Brothers chili cheese coneys recalled over undeclared sesame
Sheehan Brothers Vending Chili Cheese Coneys, 4.3 oz, are being recalled because of undeclared sesame. 377 individual units are affected.
Product
Sheehan Brothers Vending Chili Cheese Coney, 4.3 oz (120g), in a red and white paper boat and individually wrapped in plastic, UPC: 100000222027
Category
Food
Distribution
3 states
SevereFDA (Devices)·Z-2161-2025·2025-08-06
SafeStar 60A Plus breathing filters show a slow rising CO2 curve
SafeStar 60A Plus bidirectional breathing system filters are being recalled following reports of a slow increase of the CO2 curve when the gas sample is taken from the filter's port. 374,700 units affected.
Product
SafeStar 60A Plus Filter. Bidirectionally breathing system filter.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V502000·2025-08-06
2018–2025 International and IC Bus vehicles recalled for fire risk
International Motors is recalling certain 2018–2025 International 4000 Series, MV, 1300 FBC, and IC Bus TC and CECB vehicles. A leaking brake pressure switch assembly may cause an electrical short circuit that increases fire risk while driving or parked.
Product
IC BUS — IC BUS, INTERNATIONAL CECB, MV, 1300FBC, 4000 SERIES 4300
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V503000·2025-08-06
IC Bus CESB School Buses Brake Pressure Switch Fire Risk Recall
International Motors is recalling certain 2016–2024 IC Bus CESB school buses because the brake pressure switch assembly may leak brake fluid into electrical components, causing a short circuit and fire risk while driving or parked.
Product
IC BUS — IC BUS CESB
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·H-0336-2025·2025-08-06
Sheehan Brothers BBQ riblet sandwiches recalled over undeclared sesame
Sheehan Brothers Vending BBQ Riblet Sandwich with Coleslaw, 8 oz, is being recalled because of undeclared sesame. 209 individual units are affected.
Product
Sheehan Brothers Vending BBQ Riblet Sandwich with Coleslaw, 8 oz (226g), in a plastic tray/2 oz cup and individually wrapped in plastic, UPC: 100000222744
Category
Food
Distribution
3 states
HighFDA (Devices)·Z-2211-2025·2025-08-06
Philips Ingenia Elition X gradient coils may act as heat source
Ingenia Elition X MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 632 units are affected.
Product
Ingenia Elition X Model Numbers (REF): (1) 781358, (2) 782107, (3) 782119, (4) 782136, (5) 782151 (China ONLY);
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2235-2025·2025-08-06
LVP dual Y-site administration sets have potential for external cassette leaks
LVP Primary Administration Sets, Dual-Inlet, Low-Sorbing, Needle-Free Port, Dual Y-Site, are being recalled because of the potential for external cassette leaks. 348,150 units are affected.
Product
LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Dual Y-Site (Qty 25). Product Code: SET-0032-25.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2205-2025·2025-08-06
Philips Ingenia 1.5T S gradient coils may act as heat source
Ingenia 1.5T S MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 136 units are affected.
Product
Ingenia 1.5T S Model Number (REF): 781347;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2178-2025·2025-08-06
HarmonyAIR E-Series monitor yokes may detach from the spring arm
Dual Flat Panel Monitor accessories for HarmonyAIR E-Series Surgical Lighting Systems are being recalled because the yoke assembly may detach from the spring arm. 59 units are affected.
Product
Dual Flat Panel Monitor (DFPM) accessories for HarmonyAIR E-Series Surgical Lighting Systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2214-2025·2025-08-06
Philips MR 7700 gradient coils may act as a heat source
MR 7700 systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 82 units are affected.
Product
MR 7700 Model Numbers (REF): (1) 782120, (2) 782153;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2226-2025·2025-08-06
Blood MacConkey biplates may carry Listeria monocytogenes surface contamination
Blood/MacConkey Biplates, product number R02049, are being recalled because the products may contain surface and subsurface contamination of Listeria monocytogenes. 611 units are affected.
Product
Blood/MacConkey Biplate 100/PK, Product Number R02049
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2221-2025·2025-08-06
Volcano Visions IVUS catheters can entangle with the guide wire
Volcano Visions Digital IVUS Catheters are being recalled following reports of catheter and guide wire entanglement during radial-to-peripheral procedures, which may require surgical removal. 233,817 units affected.
Product
Volcano Visions Digital IVUS Catheter: PV.014P (Platinum), REF:85910P; PV.014P RX, REF: 014R; and PV.018, REF: 86700, 86700J used with Instructions for use.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2208-2025·2025-08-06
Philips Ingenia Ambition S gradient coils may act as heat source
Ingenia Ambition S MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 611 units are affected.
Product
Ingenia Ambition S Model Numbers (REF): (1) 781359, (2) 782108, (3) 782133 (China ONLY), (4) 782139;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2207-2025·2025-08-06
Philips Ingenia 3.0T CX gradient coils may act as heat source
Ingenia 3.0T CX MR systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 350 units are affected.
Product
Ingenia 3.0T CX Model Numbers (REF): (1) 781271, (2) 782105;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2232-2025·2025-08-06
LVP dual-inlet administration sets have potential for external cassette leaks
LVP Primary Administration Sets, Dual-Inlet, Low-Sorbing, Needle-Free Port, Y-Site, are being recalled because of the potential for external cassette leaks. 19,225 units are affected.
Product
LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Y-Site (Qty 25). Product Code: SET-0013-25.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2216-2025·2025-08-06
SmartPath to dStream XR gradient coils may act as heat source
SmartPath to dStream for XR and 3.0T systems are being recalled because component failures in the gradient coil may act as a heat source with the potential to produce smoke or fire. 294 units affected.
Product
SmartPath to dStream for XR and 3.0T Model Numbers (REF): (1) 781270, (2) 782113, (3) 782129;
Category
Medical Device
Distribution
Distributed nationwide