State

Indiana product recalls

73,596 recalls have nationwide distribution and so reach Indiana. 9,592 additional recalls listed Indiana specifically in their distribution scope.

What the numbers show

Total: 9,592
Critical: 1,908
Severe: 2,534
Most recent: 2026-10-24

Of the 9,592 recalls naming Indiana we have scored against our rubric, 1,908 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,534 (26%) are Severe.

Which agencies issued them

These figures cover only the 9,592 recalls whose distribution notice names Indiana specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28951–28975 of 83188

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-0937-2021·2021-02-03
Qiagen Recalls PIK3CA PCR Kits Due to False Positive Mutation Results
Qiagen Sciences LLC is recalling 575 therascreen PIK3CA RGQ PCR Kits because they may generate false positive results for the Q546R mutation, potentially affecting treatment decisions for breast cancer patients.
Product
therascreen PIK3CA RGQ PCR Kit (23) US IVD product- aid clinicians in identifying breast cancer patients who may be eligible for treatment with PIQRAY (alpelisib) based on a PIK3CA Mutation Detected result. REF 873121
Category
Medical Device
Distribution
9 states
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
HighFDA (Devices)·Z-0892-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Backup Battery Failure Risk
Respironics is recalling three V60 Ventilators due to potential backup battery failures caused by over-discharge or extended storage without AC power.
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-0886-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Backup Battery Failure Risk
Respironics is recalling 9,863 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 1053614 - 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-0910-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Navigation Ring Defects
Respironics is recalling 3,213 V60 Ventilators worldwide due to navigation ring issues that may cause erratic parameter changes or inoperability.
Product
Philips Respironics V60 Ventilator Part Number R1076709 - 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-0896-2021·2021-02-03
Philips Respironics V60 Plus Ventilator Recalled for Backup Battery Failure
Respironics is recalling 3,887 V60 Plus Ventilators because the backup battery may fail if over-discharged or stored without AC power.
Product
Philips Respironics V60 Plus Ventilator Part Number 1137276 - 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-0241-2021·2021-02-03
Cinnamon Walnut Coffee Cake Recalled for Undeclared Allergens
Nueske Applewood Smoked Meat, Inc. is recalling Cinnamon Walnut Coffee Cake because it may contain undeclared wheat, egg, milk, and walnuts.
Product
Cinnamon Walnut Coffee Cake, Item 258, Net Wt. 24 oz.
Category
Food
Distribution
23 states
HighFDA (Devices)·Z-0899-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Backup Battery Failure Risk
Respironics is recalling 481 V60 Ventilators due to potential backup battery failures caused by over-discharge or extended storage without AC power.
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.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0890-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Backup Battery Failure Risk
Respironics is recalling 534 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 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-0913-2021·2021-02-03
Philips Respironics V60 Plus Ventilator Recall Due to Navigation Ring Malfunction
The FDA is recalling the Philips Respironics V60 Plus Ventilator because its navigation ring may become inoperative or operate intermittently, potentially causing ventilator parameter values to change erratically during setup or adjustment.
Product
Philips Respironics V60 Plus Ventilator Part Number 1137276 - 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-0898-2021·2021-02-03
Philips Respironics V60 Plus Ventilator Recalled for Battery Failure Risk
Respironics is recalling 702 V60 Plus Ventilators worldwide because the backup battery may fail if over-discharged or stored without AC power.
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
HighNHTSA·21V045000·2021-02-03
Royal Enfield Recalls 2018-2020 Motorcycles for Brake Caliper Corrosion
Royal Enfield is recalling 2018-2020 Continental GT 650 and Interceptor 650 motorcycles because road salt may corrode brake calipers, potentially reducing braking performance.
Product
ROYAL ENFIELD — ROYAL ENFIELD CONTINENTAL GT 650, INTERCEPTOR 650
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21E008000·2021-02-03
Bigfoot Truck Campers Recalled for Potential Gas Leak Risk
Bigfoot Industries is recalling specific 1500 and 2500 Series truck campers because a saddle valve bolt may be overtightened, damaging the seal and causing a gas leak that increases fire risk.
Product
EQUIPMENT:APPLIANCE:OVEN/STOVE/COOKTOP recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0912-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Navigation Ring Defects
Respironics is recalling 216 V60 Ventilators because the navigation ring may fail or cause erratic parameter changes.
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 (Devices)·Z-0902-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Navigation Ring Defects
Respironics is recalling 2,137 V60 Ventilators because the navigation ring may malfunction or cause erratic parameter changes.
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-0917-2021·2021-02-03
Philips Respironics V680 Ventilator Recalled for Navigation Ring Defects
Respironics is recalling 3,453 V680 ventilators worldwide because the navigation ring may fail or cause erratic parameter changes.
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-0893-2021·2021-02-03
Philips Respironics V60 Ventilator Recalled for Backup Battery Failure Risk
Respironics is recalling 3,213 V60 Ventilators because the backup battery may fail if over-discharged or stored without AC power.
Product
Philips Respironics V60 Ventilator Part Number R1076709 - 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