State

Northern Mariana Islands product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50001–50025 of 73840

LowFDA (Drugs)·D-0660-2016·2016-02-17
Amerisource Recalls Candesartan Cilexetil Tablets Due to Impurity Failures
Amerisource Health Services is recalling 716 cartons of Candesartan Cilexetil Tablets, 16 mg, due to failed impurities and degradation specifications.
Product
Candesartan Cilexetil Tablets, 16 mg, 30 Tablets (5 x 6) blister pack, Rx, Distributed by: American Health Packaging Columbus, Ohio 43217, NDC 68084-877-25(carton), NDC 68084-877-95(individual dose)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0782-2016·2016-02-17
Zimmer Dental Implants Recalled for Missing Instructions in Manual
Zimmer Dental Inc is recalling specific Trabecular Metal implants because the latest instruction manual omitted critical safety information for certain sizes.
Product
IMPLANT,TM, MTX FULL 3.7 mm x 11.5 mm diameter 3.5 mm Catalog #TMTB11 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0777-2016·2016-02-17
Zimmer Dental Implants Recalled for Omitted Instructions
Zimmer Dental Inc. is recalling specific dental implants because important safety information was missing from the latest instruction manual.
Product
IMPLANT,TM, MTX 3.7 mm x 13 mm diameter 3.5 mm Catalog #TMMB13 Product Usage: Zimmer Dental implant systems are designed for use in the maxilla or mandible for immediate loading or for loading after a conventional healing period. Implants may be used to replace one or…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V086000·2016-02-16
Starcraft AR-One Toy Hauler Recall for Incorrect Tire Labels
Starcraft is recalling 2016 AR-One toy hauler trailers because incorrect tire labels may lead to improper tire replacement, increasing crash risk.
Product
STARCRAFT RV TT — STARCRAFT RV TT AR-ONE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V087000·2016-02-16
Mercedes-Benz Recalls 2016 C300 and C450 Models for Sunroof Defect
Mercedes-Benz is recalling specific 2016 C300 and C450 vehicles because the panoramic sunroof glass may not be properly bonded and could detach during operation.
Product
MERCEDES-BENZ — MERCEDES-BENZ C300, C450
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V088000·2016-02-16
IMT Recalls Dominator Cranes Due to Valve Bank Cover Defect
Iowa Mold Tooling is recalling 2013-2016 Dominator vehicles because a valve bank cover may crack and fall off, creating a road hazard.
Product
IMT — IMT DOMINATOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V085000·2016-02-12
Trans Tech Student Safety Transporter School Bus Barrier Recall
Transportation Collaborative is recalling 2012-2015 Trans Tech Student Safety Transporter school buses because the driver's side barrier may not deform properly in a crash.
Product
TRANS TECH BUS — TRANS TECH BUS STUDENT SAFETY TRANSPORT
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·16101·2016-02-12
Crescent Point Energy Recalls Propane Gas Due to Fire and Burn Hazards
Crescent Point Energy is recalling approximately 118 million gallons of propane gas in the U.S. because insufficient odorant levels may prevent consumers from detecting leaks, posing fire and burn risks.
Product
Propane (LP) Gas
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·16100·2016-02-11
Nuna Baby Essentials Recalls ZAAZ High Chairs Due to Fall Hazard
Nuna Baby Essentials is recalling ZAAZ high chairs because the arm bar can bend or detach, posing a fall hazard to children.
Product
High chairs
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·16V081000·2016-02-11
Mercedes-Benz and Chrysler Recall Vehicles Due to Air Bag Inflator Defect
Mercedes-Benz and Chrysler are recalling specific vehicles because the driver's frontal air bag inflator may rupture during deployment, potentially causing serious injury or death.
Product
MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ, CHRYSLER E63, ML63, GL350, GL450
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V083000·2016-02-11
Volkswagen Recalls 2009 Routan Vehicles Due to Air Bag Control Unit Defect
Volkswagen is recalling 2009 Routan vehicles because the air bag control unit may corrode and fail, potentially preventing air bag deployment or causing unintended deployment.
Product
VOLKSWAGEN — VOLKSWAGEN ROUTAN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V084000·2016-02-11
GM Recalls 2016 Vehicles for Missing Audio Safety Warnings
General Motors is recalling 2016 Chevrolet and GMC vehicles because the radio may fail to provide audio warnings for unbelted drivers or keys left in the ignition.
Product
GMC — GMC, CHEVROLET SIERRA, SILVERADO, MALIBU, CAMARO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V082000·2016-02-11
Starcraft RV Recalls 2016 Trailers Due to Water Heater Overheating Risk
Starcraft RV is recalling 2016 Solstice and Travel Star trailers because water heaters may overheat, posing a scalding risk.
Product
STARCRAFT RV FW — STARCRAFT RV FW, STARCRAFT RV TT SOLSTICE, TRAVEL STAR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V078000·2016-02-10
Volkswagen and Audi Vehicles Recalled for Air Bag Inflator Rupture Risk
Volkswagen Group of America is recalling specific 2007-2014 Volkswagen and Audi models because the driver's air bag inflator may rupture during deployment, potentially causing serious injury or death.
Product
VOLKSWAGEN — VOLKSWAGEN, AUDI EOS, CC, Q5, PASSAT
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0691-2016·2016-02-10
Draeger Oxylog 2000 Plus Ventilator Recalled for Malfunction
Draeger Medical is recalling Oxylog 2000 Plus ventilators because a software error can stop ventilation and trigger alarms.
Product
Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number: 5705080. Volume controlled emergency and transport ventilator with pressure support.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·16V079000·2016-02-10
Volkswagen Recalls Audi and Passat Vehicles for Airbag Inflator Defect
Volkswagen is recalling 151,767 Audi and Volkswagen vehicles because the driver's airbag inflator may rupture during deployment, potentially causing serious injury.
Product
AUDI — AUDI, VOLKSWAGEN A3, A4 CABRIOLET, PASSAT
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0692-2016·2016-02-10
Draeger Oxylog 3000 Ventilators Recalled for Software Error
Draeger Medical is recalling Oxylog 3000 and Oxylog 3000 Plus ventilators because a software error can stop ventilation and trigger alarms.
Product
Emergency Transport Ventilator Oxylog 3000 Ventilator and Oxylog 3000 plus Ventilator Catalog Numbers: 2M86300/2M86965 and 5704813/5704831. Volume controlled and pressure-controlled emergency and transport ventilators.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·16V077000·2016-02-10
Daimler Vans Recalls Sprinter Vehicles Due to Air Bag Inflator Rupture Risk
Daimler Vans is recalling 2007-2014 Dodge, Freightliner, and Mercedes-Benz Sprinter vans because the driver's air bag inflator may rupture during deployment.
Product
FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ, DODGE SPRINTER 2500, SPRINTER 3500
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0745-2016·2016-02-10
Philips Proton Therapy Planning Software Recalled for Dose Calculation Errors
Philips Medical Systems is recalling DS/US Proton Feature software due to a defect that may cause incorrect dose calculations in radiation therapy planning.
Product
DS/US Proton Feature with Pinnacle3 Software Version 10.0.0 and 14.0.0 Radiation Therapy Planning System Model #459800200621
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0710-2016·2016-02-10
Philips Allura Xper OR Table Recall for Image Interpretation Risk
Philips is recalling Allura Xper FD20 OR Tables because live and still images may be misinterpreted, potentially affecting diagnostic accuracy.
Product
Allura Xper FD20 OR Table; Model Numbers: 722035 722023 Dedicated vascular and neurovascular imaging applications, including diagnostic and interventional procedures. This includes, e.g. peripheral, cerebral, thoracic and abdominal angiography, as well as PTCAs, stent…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0720-2016·2016-02-10
Philips INTEGRIS and Allura Systems Recalled for Image Interpretation Error
Philips is recalling INTEGRIS and Allura medical imaging systems because a software issue may cause still images to be misinterpreted as live images.
Product
INTEGRIS BH3000; Model Number: 72242 The Philips INTEGRIS 3000 I 5000 system is intended for interventional and diagnostic vascular and neurovascular procedures. The Philips INTEGRIS Allura 9 Biplane system is intended for diagnostic cardiovascular, vascular and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0707-2016·2016-02-10
Philips Allura Xper FD20 Recall for Image Interpretation Error
Philips is recalling Allura Xper FD20 systems because still images may be misinterpreted as live images, potentially affecting diagnostic accuracy.
Product
Allura Xper FD20; Model Numbers: 722028 722012 722006 Dedicated vascular and neurovascular imaging applications, including diagnostic and interventional procedures. This includes, e.g. peripheral, cerebral, thoracic and abdominal angiography, as well as PTCAs, stent…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0756-2016·2016-02-10
BioMerieux Recalls API ZYM Bx2 Reagent Due to False Negative Results
BioMerieux SA is recalling API ZYM Bx2 reagent because it produces false negative results, leading to discrepant identification outcomes in laboratory tests.
Product
API ZYM Bx2 (Ref 70493) Product Usage: ZYM B reagent is an additional test used for revealing the results of some miniaturized biochemical test including in the involved API strips.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·16099·2016-02-10
Pier 1 Imports Recalls Capella Island Swivel Dining Chairs Due to Fall Hazard
Pier 1 Imports is recalling Capella Island Swivel Dining Chairs because the base can break, posing a fall hazard to users.
Product
Capella Island Swivel Dining Chairs
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0735-2016·2016-02-10
MediChoice Cohesive Bandages Recalled for Microbial Contamination
Owens & Minor is recalling MediChoice sterile cohesive bandages because testing revealed microbial contamination.
Product
MediChoice Cohesive Bandages, One (1) roll of cohesive bandage per bag, thirty-six (36) bags per case [all model numbers have equivalent packaging] General Hospital Use.
Category
Medical Device
Distribution
Distributed nationwide