State

Northern Mariana Islands product recalls

73,495 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 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24001–24025 of 73518

HighFDA (Devices)·Z-2161-2021·2021-08-04
OEC Elite Mobile C-Arm Recalled for Battery Depletion
GE OEC Medical Systems is recalling 3,570 OEC Elite mobile C-arm imaging systems worldwide due to potential early depletion of the battery that monitors X-ray tube temperature, which could render the system inoperable.
Product
OEC Elite mobile C-arm - Product Usage: intended to provide fluoroscopic and digital spot images of the patient anatomy, interventional tools/devices, and contrast agents during diagnostic, interventional, and surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2151-2021·2021-08-04
CooperVision Contact Lenses Recalled for Misaligned Axis Mark
CooperVision is recalling MEDIFLEX ELITE 1 DAY TORIC daily disposable contact lenses (lot W0106167) due to misaligned axis marks that can cause blurred vision.
Product
MEDIFLEX ELITE 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V605000·2021-08-04
Bentley Recalls 2021 Bentayga Vehicles Due to Seat Belt Retractor Defect
Bentley is recalling 2021 Bentayga vehicles because front passenger seat belt retractors may deactivate early, preventing child restraints from securing properly.
Product
BENTLEY — BENTLEY BENTAYGA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V608000·2021-08-04
2021 Porsche Taycan Seat Belt Retractor Defect May Prevent Child Restraint Securing
Porsche is recalling certain 2021 Taycan models because the seat belt automatic locking retractors may deactivate early, preventing child restraint systems from securing properly during a crash.
Product
PORSCHE — PORSCHE 911, PANAMERA 4S, PANAMERA 4 E-HYBRID, PANAMERA TURBO S
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·21174·2021-08-04
Two Million Dehumidifiers Recalled for Fire and Burn Hazards
About 2 million dehumidifiers manufactured by New Widetech under multiple brand names are recalled because they can overheat and catch fire, posing fire and burn hazards. Consumers should stop using them immediately.
Product
Dehumidifiers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2150-2021·2021-08-04
Contact lens recall: misaligned axis mark may cause blurred vision
CooperVision is recalling CLARITI 1 DAY TORIC contact lenses (Lot W0106167) due to misaligned axis marks that may cause blurred vision. The recall affects 450 lenses distributed across select U.S. states and multiple countries.
Product
CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2149-2021·2021-08-04
CLARITI 1 DAY TORIC Contact Lenses Recalled Due to Axis Mark Misalignment
CooperVision is recalling CLARITI 1 DAY TORIC contact lenses (Lot W0106167) due to misaligned axis marks that can cause blurred vision. Affected patients should discontinue use and contact their eye care provider.
Product
CLARITI 1 DAY TORIC -DIAGNOSTIC Power-07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2144-2021·2021-08-04
Contact Lens Axis Mark Misalignment May Cause Blurred Vision
CooperVision's AQUATECH PLUS 1 DAY TORIC contact lenses (lot R0121629) have misaligned axis marks that may cause blurred vision in patients.
Product
AQUATECH PLUS 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2163-2021·2021-08-04
Coaxial Interventional Needles recalled for potential sterilization failure
Coaxial Interventional Needles from INNOVATIVE TOMOGRAPHY PRODUCT GMBH may not be properly sterilized. Multiple lot numbers are affected and should not be used.
Product
Coaxial Interventional Needle, ITP innotom.com, CE 0297, STERILE EO for the following article numbers: Article no. KIR 23/05, Length 50 mm, Diameter 23 G (0.6 mm); Article no. KIR 23/05N, Length 50 mm, Diameter 23 G (0.6 mm); Article no. KIR 23/07, Length 75 mm, Diameter…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21E071000·2021-08-04
Enerco Propane Regulators Recalled Due to Fire Risk
Enerco Group is recalling specific propane regulators that may fail, causing excessive gas pressure and increased fire risk.
Product
EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2146-2021·2021-08-04
CooperVision CLARITI 1 DAY TORIC contact lenses recalled for axis mark misalignment
CooperVision is recalling CLARITI 1 DAY TORIC daily disposable contact lenses due to misaligned axis marks that can cause blurred vision. Affected lenses in lot U0108833 were distributed in seven US states and internationally.
Product
CLARITI 1 DAY TORIC Power -07.00 -1.75/170 Daily Disposable Contact Lens with UV blocker
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V609000·2021-08-04
Peterbilt 220 Recall for Stator Assembly Wire Crimping Defect
PACCAR is recalling 2020 Peterbilt 220 trucks with Meritor 14Xe ePowertrains due to insufficiently crimped stator wires that may cause overheating and loss of drive power.
Product
PETERBILT — PETERBILT 220
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2166-2021·2021-08-04
Medical inflation device recalled due to handle separation risk
Merit Medical Systems is recalling basixALPHA Inflation Devices due to a design flaw where the syringe handle can separate when withdrawn, affecting device functionality.
Product
basixALPHA Inflation Device 30 atm/bar 20 mL - Product Usage: Used to inflate and deflate an angioplasty balloon or other interventional device, and to measure the pressure within the balloon.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V604000·2021-08-04
Newmar Motorhomes Recalled for Potential Fuel Leak and Fire Risk
Newmar Corporation is recalling certain 2021-2022 motorhomes (New Aire, Ventana, and Dutch Star) with Cummins L9 diesel engines due to potential fuel leaks that could increase fire risk. Affected owners should contact Newmar customer service at 1-800-731-8300 for free fuel hose replacement.
Product
NEWMAR — NEWMAR NEW AIRE, DUTCH STAR, VENTANA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2164-2021·2021-08-04
Semi-automatic Biopsy Needles Recalled Due to Sterilization Defect
INNOVATIVE TOMOGRAPHY PRODUCT GMBH is recalling semi-automatic biopsy needles because labeled sterile units may not have been adequately sterilized. Affected devices distributed in California should not be used.
Product
Semi-automatic Biopsy-Needle, ITP innotom.com, CE 0297, STERILE EO for the following article numbers: Article no. BIM 18/10, Length 100 mm, Diameter 18 G (1.25 mm); Article no. BIM 18/15, Length 150 mm, Diameter 18 G (1.25 mm); Article no. BIM 18/20, Length 200 mm…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V603000·2021-08-04
Lamborghini Recalls 2021 Urus for Rear Seat Belt Retract Defect
Lamborghini is recalling 2021 Urus vehicles because middle-rear seat belt retractors may deactivate early, preventing child restraints from securing properly.
Product
LAMBORGHINI — LAMBORGHINI URUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2160-2021·2021-08-04
OEC 3D Imaging X-Ray Systems Recalled for Coin Cell Battery Depletion
GE OEC Medical Systems is recalling certain OEC 3D Imaging fluoroscopic X-ray systems due to potential premature depletion of the coin cell battery used to monitor X-ray tube temperature, which could cause the system to become inoperable.
Product
OEC 3D Imaging, Image-Intensified Fluoroscopic X-Ray System, Mobile - Product Usage: designed to provide fluoroscopic and digital spot images of adult and pediatric populations during diagnostic, interventional, and surgical procedures
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2156-2021·2021-08-04
Affinity Four Birthing Bed Latch Mechanism Defect Poses Fall Risk
The latch mechanism on the Lift-Off foot section of certain Affinity Four Birthing Beds may be damaged, potentially causing improper engagement and creating a fall risk for patients. Hill-Rom is recalling approximately 1,096 affected beds.
Product
Affinity Four Birthing Bed-used as a birthing bed for women of child bearing age in an LDR (Labor, Delivery, Recovery) or LDRP (Labor, Delivery, Recovery, Postpartum) setting within the acute care Labor and Delivery market Model Numbers: P3700B, P3700C, P3700D, & P3700E
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2162-2021·2021-08-04
Coaxial Interventional Needles Recalled for Potential Sterilization Defects
INNOVATIVE TOMOGRAPHY PRODUCT GMBH is recalling Coaxial Interventional Needles distributed in California due to potential sterilization defects. Needles labeled as sterile may not have been adequately sterilized, creating infection risks.
Product
Coaxial Interventional Needle, ITP innotom.com, CE 0297, STERILE EO for the following article numbers: Article no. KIM 22/05, Length 50 mm, diameter 22G/0,7 mm; Article no. KIM 22/07,Length 75 mm, diameter 22 G (0.7 mm); Article no. KIM 22/10, Length 100 mm, diameter 22 G…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V607000·2021-08-04
2021 Volkswagen ID.4 rear seat belt assemblies may not secure child restraints
Certain 2021 Volkswagen ID.4 vehicles have rear seat belt assemblies without proper automatic locking function, preventing child restraint systems from securing correctly. Dealers will inspect and replace affected assemblies at no cost.
Product
VOLKSWAGEN — VOLKSWAGEN ID.4
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2154-2021·2021-08-04
Daily Toric Contact Lenses Recalled for Misaligned Axis Mark
CooperVision is recalling SOFMED BREATHABLES 1 DAY TORIC contact lenses (Lot W0106167) due to misaligned axis marks that can cause blurred vision. Affected lenses were distributed in the US and internationally.
Product
SOFMED BREATHABLES 1 DAY TORIC Power-07.00 -1.75/ 170 Daily Disposable Contact Lens with UV blocker
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2148-2021·2021-08-04
Contact Lens Recall: Misaligned Axis Mark May Cause Blurred Vision
CooperVision is recalling SPECSAVERS UMERE TORIC daily disposable contact lenses with UV blocker due to a manufacturing defect in which misaligned axis marks may cause blurred vision.
Product
SPECSAVERS UMERE TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2139-2021·2021-08-04
GE CARESCAPE PDM monitor SpO2 display freezes during extended use
GE Healthcare's CARESCAPE PDM-Masimo SpO2 physiological monitor displays can freeze after extended use without power down, preventing real-time oxygen saturation monitoring.
Product
CARESCAPE PDM-Masimo SpO2. Physiological data monitor.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2143-2021·2021-08-04
Contact Lens Recall: Misaligned Axis Mark May Cause Blurred Vision
CooperVision is recalling CLARITI 1 DAY TORIC contact lenses with misaligned axis marks that may cause blurred vision. The defective lenses were distributed worldwide including multiple U.S. states.
Product
CLARITI 1 DAY TORIC Power: -07.50 -0.75/060 Daily Disposable Contact Lens with UV blocker
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2147-2021·2021-08-04
CooperVision CLARITI Contact Lenses Recalled for Misaligned Axis Marks
CooperVision is recalling CLARITI 1 DAY TORIC contact lenses (Lot U0108940) because misaligned axis marks can cause blurred vision in patients.
Product
CLARITI 1 DAY TORIC Power -07.00 -1.25/180 Daily Disposable Contact Lens with UV blocker
Category
Medical Device
Distribution
Distributed nationwide