State

Arkansas product recalls

73,584 recalls have nationwide distribution and so reach Arkansas. 5,543 additional recalls listed Arkansas specifically in their distribution scope.

What the numbers show

Total: 5,543
Critical: 1,027
Severe: 1,448
Most recent: 2026-10-14

Of the 5,543 recalls naming Arkansas we have scored against our rubric, 1,027 (19%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,448 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,543 recalls whose distribution notice names Arkansas specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27626–27650 of 79127

HighFDA (Devices)·Z-0916-2021·2021-02-03
Philips Respironics V60 Ventilator Recall for Navigation Ring Defects
Respironics is recalling V60 ventilators because the navigation ring may fail or cause erratic parameter changes.
Product
Philips Respironics V60 Ventilator Part Number DU1053617 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories. Philips Respironics V60 Ventilator Part Number…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0904-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Navigation Ring and Liquid Ingress Issues
Respironics is recalling 934 V60 Ventilators worldwide due to potential navigation ring malfunctions and liquid ingress risks.
Product
Philips Respironics V60 Ventilator Part Number 1053615 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0885-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Backup Battery Failure Risk
Respironics is recalling 2,144 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power for extended periods.
Product
Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0911-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Navigation Ring Defect
Respironics is recalling 10,291 V60 ventilators worldwide due to a navigation ring that may fail or cause erratic parameter changes.
Product
Philips Respironics V60 Ventilator Part Number 1076716 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V047000·2021-02-03
Bigfoot Recalls 2020-2021 2500 Series RVs Due to Gas Leak Risk
Bigfoot Industries is recalling 2020-2021 2500 Series recreational vehicles because a stove saddle valve bolt may be overtightened, causing a gas leak and fire risk.
Product
BIGFOOT — BIGFOOT 2500 SERIES
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0901-2021·2021-02-03
Philips Respironics V680 Ventilator Recalled for Backup Battery Failure Risk
Respironics is recalling 3,453 V680 Ventilators because the backup battery may fail if over-discharged or stored without AC power.
Product
Philips Respironics V680 Ventilator Part Number 850011 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0889-2021·2021-02-03
Philips Respironics V60 Ventilator Recall for Backup Battery Failure Risk
Respironics is recalling 46,313 V60 Ventilators worldwide due to a risk of backup battery failure if over-discharged or stored without AC power.
Product
Philips Respironics V60 Ventilator Part Number 1053617 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0905-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Navigation Ring and Liquid Ingress Issues
Respironics is recalling V60 Ventilators because the navigation ring may malfunction or cause erratic parameter changes, and liquid may enter the device.
Product
Philips Respironics V60 Ventilator Part Number 1053616 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0909-2021·2021-02-03
Philips Respironics V60 Ventilator Recall for Navigation Ring Defects
Respironics is recalling three V60 ventilators because the navigation ring may malfunction or cause erratic parameter changes.
Product
Philips Respironics V60 Ventilator Part Number R1053618 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0907-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Navigation Ring Defects
Respironics is recalling 534 V60 Ventilators worldwide due to navigation ring malfunctions that may cause erratic parameter changes or inoperability.
Product
Philips Respironics V60 Ventilator Part Number 1053618 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0891-2021·2021-02-03
Philips Respironics V60 Ventilator Recall for Backup Battery Failure Risk
Respironics is recalling 3,752 V60 Ventilators worldwide due to a risk of backup battery failure if over-discharged or stored without AC power.
Product
Philips Respironics V60 Ventilator Part Number 1076709 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V043000·2021-02-03
Lexus Recalls RX350 Vehicles for Potential Fuel System Fire Risk
Lexus is recalling 2019 and 2021 RX350 vehicles because a transport hook may not have been removed, which could damage the fuel filler pipe in a crash and increase fire risk.
Product
LEXUS — LEXUS RX350
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V042000·2021-02-03
Mercedes-Benz Sprinter 3500 Recalled for Electronic Stability Control Defect
Daimler Vans USA is recalling 2012-2018 Mercedes-Benz and Freightliner Sprinter 3500 campers because the Electronic Stability Control unit may become disabled, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 3500
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0894-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Backup Battery Failure Risk
Respironics is recalling 10,441 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power for extended periods.
Product
Philips Respironics V60 Ventilator Part Number 1076716 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0888-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Backup Battery Failure Risk
Respironics is recalling 330 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power for extended periods.
Product
Philips Respironics V60 Ventilator Part Number 1053616 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0900-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Backup Battery Failure Risk
Respironics is recalling 292 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power.
Product
Philips Respironics V60 Ventilator Part Number U1053617 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0895-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Potential Backup Battery Failures
Respironics is recalling 216 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power for extended periods.
Product
Philips Respironics V60 Ventilator Part Number 1076717 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0240-2021·2021-02-03
Nueske Applewood Blueberry Blizzard Coffee Cake Recalled for Undeclared Allergens
Nueske Applewood Smoked Meat, Inc. is recalling 18 units of Blueberry Blizzard Coffee Cake because the product may contain undeclared wheat, egg, and milk.
Product
Blueberry Blizzard Coffee Cake, Item 259, Net Wt. 24 oz.
Category
Food
Distribution
23 states
HighFDA (Devices)·Z-0887-2021·2021-02-03
Philips Respironics V60 Ventilator Recall for Backup Battery Failure Risk
Respironics is recalling 934 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power.
Product
Philips Respironics V60 Ventilator Part Number 1053615 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0914-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Navigation Ring Defects
Respironics is recalling 834 V60 ventilators because the navigation ring may malfunction or cause erratic parameter changes.
Product
Philips Respironics V60 Ventilator Part Number 1137292 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0906-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Navigation Ring Defect
Respironics is recalling V60 Ventilators because the navigation ring may malfunction or cause erratic parameter changes.
Product
Philips Respironics V60 Ventilator Part Number 1053617 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0897-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Backup Battery Failure Risk
Respironics is recalling 835 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power for extended periods.
Product
Philips Respironics V60 Ventilator Part Number 1137292 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1767-2020·2021-02-03
Philips Telemetry Transceiver Recall for Heart Rate Display Failure
Philips is recalling TRx4841A telemetry transceivers because they may fail to display heart rates or alarms when used with specific Patient Information Center software.
Product
TRx4841A 1.4 GHz IntelliVue Tele TRX, Model Number 862439; Includes System Codes 453564007261, 453564007271, 453564007281, 989803196951
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V048000·2021-02-03
Yamaha Recalls Motorcycles and Scooters Due to Incorrect VIN Labels
Yamaha is recalling 2019-2021 motorcycles and scooters because the VIN on the certification label may not match the vehicle, potentially preventing owners from receiving safety recalls.
Product
YAMAHA — YAMAHA YZF-R3, MT-03, CZD300
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0915-2021·2021-02-03
Philips Respironics V60 Plus Ventilator Recalled for Navigation Ring Issues
Respironics is recalling V60 Plus ventilators because the navigation ring may fail or cause erratic parameter changes.
Product
Philips Respironics V60 Plus Ventilator Part Number 1138747 - Product Usage: intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide