State

Northern Mariana Islands product recalls

73,566 recalls have nationwide distribution and so reach Northern Mariana Islands. 23 additional recalls listed Northern Mariana Islands specifically in their distribution scope.

What the numbers show

Total: 23
Critical: 0
Severe: 18
Most recent: 2026-09-23

Of the 23 recalls naming Northern Mariana Islands we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 18 (78%) are Severe.

Which agencies issued them

These figures cover only the 23 recalls whose distribution notice names Northern Mariana Islands specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26101–26125 of 73589

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
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 (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
HighFDA (Devices)·Z-0908-2021·2021-02-03
Philips Respironics V60 Ventilator Recall for Navigation Ring Issues
Respironics is recalling 3,752 V60 Ventilators worldwide due to potential navigation ring malfunctions that may cause erratic parameter changes or inoperability.
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
HighFDA (Devices)·Z-1766-2020·2021-02-03
Philips Telemetry Transceiver Recall for Heart Rate Display Failure
Philips is recalling 21,672 telemetry transceivers because they may fail to display heart rates or generate alarms when used with specific Patient Information Center software.
Product
TRx4851A 2.4 GHz IntelliVue Tele TRX, Model Number 862231; Includes Service Numbers 453564052401, 453564052411, 453564052441, 453564052451, 453564166851, 453564166861
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0918-2021·2021-02-03
Fujifilm Synapse PACS Software Recalled for Clinical Reporting Errors
Fujifilm Medical Systems is recalling Synapse PACS Software versions 7.0.0 and 7.0.1 because the software fails to update measurements when ventricular traces are changed by different users.
Product
FUJIFILM Synapse PACS Software: versions 7.0.0 and 7.0.1 - Product Usage: intended for use as a web based application on an off-the shelf PC which meets or exceeds minimum specifications and is networked with a FUJIFILM Synapse PACS server.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0242-2021·2021-02-03
Good & Gather Four Cheese Gnocchi Recalled for Foreign Material
EMILIA FOODS SRL is recalling Good & Gather Four Cheese Gnocchi because the product may contain foreign material.
Product
Good & Gather Four Cheese Gnocchi, Net Wt. 16 oz. (454g), Keep Frozen. Needs to be Fully Cooked. UPC 0 85239-10366 1 Product of Italy. Dist by Target Corporation, Minneapolis, MN 55403
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0930-2021·2021-02-03
B. Braun Introcan IV Safety Catheters Recalled for Lack of FDA Approval
Braxton Medical Corporation is recalling B. Braun Introcan IV Safety Catheters because the products do not have FDA approval for sale in the United States.
Product
B. Braun Introcan IV Safety Catheters, sterile - Product Usage: It is a single-use device to generate intravascular and tissue access to sample blood, monitor blood pressure, or administer fluids and blood intravascular.
Category
Medical Device
Distribution
Distributed nationwide