The Recall Desk

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.

47126–47150 of 73840

  • HighFDA (Devices)·Z-2353-2016·2016-08-17

    Stryker S3 MedSurg Bed Fowler Control Failure Recall

    Stryker is recalling S3 MedSurg Beds because CPU board failures can cause the backrest electronic controls to stop working.

    Product
    S3 MedSurg Bed, Model 3005. Stryker Medical
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2352-2016·2016-08-17

    Ortho VITROS Estradiol Reagent Recall Due to Fulvestrant Cross-Reactivity

    Ortho Clinical Diagnostics is recalling VITROS Estradiol Reagent Packs because the drug Fulvestrant causes falsely high test results in postmenopausal women.

    Product
    VITROS Immunodiagnostic Products Estradiol Reagent Pack, Unique Device Identifier No. 10758750005017, REF/Catalog Number/Product Code 855 2630; IVD -- Ortho-Clinical Diagnostics, Pencoed, Bridgend CF35 5PZ, UK --- The VITROS Estradiol test is performed using the VITROS Estradiol…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2390-2016·2016-08-17

    Stryker Triathlon Tibial Alignment Handle Recalled Due to Weld Defect

    Stryker Howmedica Osteonics is recalling 47 units of the Specialty Triathlon Tibial Alignment Handle because the secondary locking mechanism may disassociate during surgery due to a weld defect.

    Product
    Stryker Orthopaedics Specialty Triathlon Tibial Alignment Handle with Secondary Lock, Non-Sterile, Used to complement or replace the standard instruments used during the implantation of hip, knee, trauma and upper extremities implants
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2377-2016·2016-08-17

    Stryker Recalls Triathlon Modular Handle Instruments Due to Fit Issues

    Stryker Howmedica Osteonics is voluntarily recalling Triathlon Modular Handle instruments because press fit specifications were not met, potentially causing disassociation.

    Product
    Stryker Orthopaedics Modular Handle Triathlon Instruments, Non-Sterile, REF 6541-4-808, Lot 123, NDC M546654148080S Product Usage: Is a reusable instrument that is part of the Triathlon Primary total knee arthroplasty (TKA) system as well as the Triathlon Partial Knee…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2344-2016·2016-08-17

    Siemens Artis Angiography Systems Recalled for Image Reproduction Failure

    Siemens Medical Solutions is recalling 51 Artis zee and Artis Q angiography systems due to a software error that may cause image loss after startup.

    Product
    Artis zee/ zeego, Artis Q/ Q.zen, stand alone system, software controlled Model numbers: 10094135, 10094137, 10094139, 10094141, 10280959, 10848281, 10848282, 10848283, 10848353, 10848255 Artis zee / zeego and Q/ Q.zen is a family of dedicated angiography systems developed for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2394-2016·2016-08-17

    Siemens AXIOM Artis X-Ray Systems Recalled for Cooling System Contamination

    Siemens is recalling AXIOM Artis angiography systems because biomass contaminants in the cooling system may damage the pump.

    Product
    ARTIS ZEE AND ZEEGO, system, x-ray, angiographic AXIOM Artis, Artis zee / zeego and Artis Q/ Q.zen are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2405-2016·2016-08-17

    Topcon Recalls PASCAL Synthesis Ophthalmic Laser Systems Due to Titration Anomaly

    Topcon Medical Laser Systems is recalling 205 PASCAL Synthesis ophthalmic laser systems worldwide due to a software anomaly affecting the titration process when specific functions are used.

    Product
    Opthalmic: PASCAL Synthesis is an ophthalmic scanning laser system. The system can perform single shot photocoagulation as is performed conventionally.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2395-2016·2016-08-17

    Siemens Medical Solutions Recalls Artis Q and Q.Zen Angiography Systems

    Siemens Medical Solutions is recalling Artis Q and Q.Zen angiography systems because biomass in the cooling system may damage the pump.

    Product
    ARTIS Q AND Q.ZEN- MODULAR ANGIOGRAPHIC SYSTEM, interventional fluoroscopic x-ray system22 AXIOM Artis, Artis zee / zeego and Artis Q/ Q.zen are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2375-2016·2016-08-17

    Nobel Biocare Recalls Guided Surgery Kit Instructions for Incorrect Drill Protocol

    Nobel Biocare is recalling 231 Guided Surgery Kits because the Instructions for Use contain an incorrect drill protocol. The kits are used for NobelParallel CC Implants.

    Product
    Instructions for Use (IFU) and Manual NobPrl CC Guided Surgery Kit Instructions for Use (IFU): "NobelGuide for NobelParallel Conical Connection", id # 2002 and Manual: Guided Surgery with NobelParallel Conical Connection", id # 79423. Article # 38072, Nobel Parallel CC Guided…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2393-2016·2016-08-17

    Siemens AXIOM Artis Angiography Systems Recalled for Cooling System Contamination

    Siemens is recalling AXIOM Artis angiography systems because biomass contamination in the cooling system may damage the pump.

    Product
    AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM, system, x-ray, angiographic AXIOM Artis, Artis zee / zeego and Artis Q/ Q.zen are a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2378-2016·2016-08-17

    BD Tritest CD3/CD4/CD45 Reagent Recalled for Incorrect Labeling

    Becton, Dickinson and Company is recalling 14,089 vials of BD Tritest CD3 FITC/CD4 PE/CD45 PerCP because the label incorrectly states the product contains gelatin.

    Product
    BD Tritest CD3 FITC/CD4 PE/CD45 PerCP (IVD); Catalog number 340383. Label states: Contains CD3 FITC/CD4 PE/CD45 per CP with Gelatin and 0.1% sodium azide. Hematology: BD Tritest CD3 fluorescein isothiocyanate (FITC)/CD4 phycoerythrin (PE)/CD45 peridinin chlorophyll…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V606000·2016-08-16

    KME Predator Emergency Vehicles Recalled for Front Grille Separation Risk

    Kovatch Mobile Equipment is recalling 27 KME Predator emergency vehicles from 2012-2013 because the front grille may loosen and separate from the cab, creating a road hazard.

    Product
    KME — KME PREDATOR PUMPER, PREDATOR RESCUE, PREDATOR AERIAL, PREDATOR PANTHER PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V603000·2016-08-16

    Mercedes-Benz Recalls 2016 C300 and GLC300 for Electronic Stability Control Defect

    Mercedes-Benz is recalling 2016 C300 and GLC300 vehicles because a damaged Electronic Stability Program control unit may activate stability control or disable the parking brake, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ C300, GLC300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V599000·2016-08-15

    Autocar Recalls 2016-2017 Xspotter Vehicles for Steering Column Defect

    Autocar is recalling 294 model year 2016-2017 Xspotter vehicles because a steering column shaft weld may break, causing a loss of steering ability and increasing crash risk.

    Product
    AUTOCAR — AUTOCAR XSPOTTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V601000·2016-08-15

    Spartan Motors Recalls 2014-2016 Legend and Star Fire Trucks

    Spartan Motors is recalling 2014-2016 Legend and Star fire trucks due to a transmission defect that may prevent power output switching, risking injury.

    Product
    SPARTAN ERV — SPARTAN ERV LEGEND, STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V600000·2016-08-15

    Keystone Recalls 2011-2017 Bullet and Passport Trailers for Fire Risk

    Keystone is recalling 2011-2017 Bullet and Passport recreational trailers because an improperly wired air conditioner thermostat may cause an electrical short and fire.

    Product
    KEYSTONE — KEYSTONE PASSPORT, BULLET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V602000·2016-08-15

    Mercedes-Benz Recalls 2016 GLE450 for Rear Head Restraint Defect

    Mercedes-Benz is recalling 2016 GLE450 vehicles because rear head restraints may not stay locked in very low temperatures, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V596000·2016-08-12

    Toyota Recalls RAV4 and Lexus HS 250h for Rear Suspension Defect

    Toyota is recalling 2006-2011 RAV4 and 2010 Lexus HS 250h vehicles because improperly tightened rear suspension arms may fail, causing loss of vehicle control.

    Product
    TOYOTA — TOYOTA, LEXUS RAV4, HS 250 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V597000·2016-08-12

    Harbor Freight Recalls Haul Master Trailers for Rear Lamp Bracket Defect

    Harbor Freight is recalling 2006-2016 Haul Master trailers because incorrectly positioned rear lamp brackets may fail to illuminate the license plate, increasing crash risk.

    Product
    HAUL MASTER — HAUL MASTER TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V598000·2016-08-12

    Winnebago Recalls 2015-2017 Recreational Vehicles Due to Electrical Fire Risk

    Winnebago is recalling 2015-2017 Itasca and Winnebago recreational vehicles because a loose electrical connection may cause heat buildup and increase the risk of a fire.

    Product
    ITASCA — ITASCA, WINNEBAGO CAMBRIA, SUNSTAR, ASPECT, ERA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16T011000·2016-08-12

    Goodyear Recalls Dunlop SP50 Tires Due to Tread Chunking Risk

    Goodyear is recalling specific Dunlop SP50 tires manufactured between December 2012 and February 2014 because they may experience tread chunking, which increases the risk of a crash.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V593000·2016-08-11

    Mazda Recalls CX-7 Vehicles Due to Front Suspension Corrosion Risk

    Mazda is recalling 2007-2012 CX-7 vehicles because water and salt may cause front suspension ball joints to corrode and separate, potentially leading to a loss of steering control.

    Product
    MAZDA — MAZDA CX-7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V595000·2016-08-11

    GM Recalls 2016 Buick Verano Vehicles Due to Fuel Line Fire Risk

    General Motors is recalling 2016 Buick Verano vehicles because a misrouted fuel line may contact the engine, wear, and leak fuel, increasing the risk of a fire.

    Product
    BUICK — BUICK VERANO
    Category
    Vehicle
    Distribution
    Distributed nationwide