The Recall Desk

State

Northern Mariana Islands product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36526–36550 of 73760

  • ModerateFDA (Devices)·Z-0095-2019·2018-10-17

    GE Healthcare CARESCAPE Monitor B450 Recalled for Network-Related Restart Issues

    GE Healthcare is recalling CARESCAPE Monitor B450 units because they may restart simultaneously and fail to complete the process if connected to an overloaded network.

    Product
    GE Healthcare CARESCAPE Monitor B450 Product Usage: Intended uses of CARESCAPE B450 in 510(k) countries [UR_CRSCP-885]: The CARESCAPE Monitor B450 is a multi-parameter patient monitor intended for use in multiple areas and intrahospital transport within a professional…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0096-2019·2018-10-17

    GE Healthcare CARESCAPE Monitor B850 Recalled for Network-Related Restart Issues

    GE Healthcare is recalling CARESCAPE Monitor B850 units because they may simultaneously restart during prolonged network overload, preventing the restart from completing until the network issue is corrected.

    Product
    GE Healthcare CARESCAPE Monitor B850 Product Usage: Intended uses of CARESCAPE B850 V2 in 510(k) countries [UR_CRSCP-1046]: The CARESCAPE Monitor B850 is a multi-parameter high acuity patient monitor intended for use in multiple areas within a professional healthcare…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0012-2019·2018-10-17

    InvaGen Recalls Amlodipine Besylate Tablets Due to Subpotency

    InvaGen Pharmaceuticals is recalling one lot of Amlodipine Besylate 10 mg tablets because the product failed to meet assay specifications at 3-month stability conditions.

    Product
    AMLODIPINE BESYLATE — AMLODIPINE BESYLATE (AMLODIPINE BESYLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0088-2019·2018-10-17

    GSK Recalls Prevacid 24HR Capsules Due to Manufacturing Deviations

    GSK is voluntarily recalling Prevacid 24HR capsules nationwide due to Current Good Manufacturing Practice (CGMP) deviations. No illnesses have been reported.

    Product
    Prevacid 24HR (Lansoprazole) delayed-release capsules, 15 mg, 14 capsules per bottle in a carton containing 1 bottle (NDC: 0067-6286-14), 2 bottles (NDC: 0067-6286-28) or 3 bottles (NDC: 0067-6286-42), Over-the-counter, Distributed By: GSK Consumer Healthcare, Warren, NJ 07059.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0011-2019·2018-10-17

    Jubilant Cadista Recalls Pantoprazole Tablets Due to Dark Discoloration

    Jubilant Cadista Pharmaceuticals is recalling 158,466 bottles of 40 mg pantoprazole sodium delayed-release tablets due to dark discoloration or brown spots on the edges.

    Product
    Pantoprazole Sodium Delayed-Release Tablets, USP, 40 mg*, 90-count bottle, Rx only, Manufactured by: Jubilant Generics Ltd., Roorkee - 247661, India; Marketed by: Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801; NDC 59746-284-90.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0016-2019·2018-10-17

    Xiromed Recalls Altavera Tablets Due to Generic Name Mislabeling

    Xiromed LLC is recalling Altavera tablets because the generic name on the packaging may cause confusion. The FDA classifies this as a Class III recall.

    Product
    ALTAVERA — ALTAVERA (LEVONORGESTREL AND ETHINYL ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0081-2019·2018-10-17

    BD FocalPoint Slide Profiler Recalled for Temperature Limit Labeling Error

    Becton Dickinson is recalling BD FocalPoint Slide Profiler and GS Review Station units because they may not function below 15°C. The agency states this issue has no potential to cause harm.

    Product
    BD FocalPoint Slide Profiler and BD FocalPoint GS Review Station; Catalog Nos. 490398, 490653, 491085, 491086, 491090, 490189 The BD FocalPoint GS Imaging System is intended to assist in cervical cancer screening of BD SurePath Liquid-based Pap Test slides to detect evidence…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V728000·2018-10-16

    Altec Recalls 2015-2017 Aerial Devices Due to Fire Risk

    Altec is recalling 2015-2017 TA45M and AM50/55 aerial devices because a faulty DC-DC converter can cause a fire.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18E096000·2018-10-16

    Streetcar Recalls Aftermarket Suspension Kits for RAM Trucks

    Streetcar ORV LLC is recalling aftermarket suspension kits for 2013-2018 RAM 2500 and 3500 trucks because improper installation may weaken the steering connection, increasing crash risk.

    Product
    RAM — RAM 3500, 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V729000·2018-10-16

    Grand Design Recalls 2019 Reflection Travel Trailers Due to Wiring Defect

    Grand Design is recalling 2019 Reflection travel trailers because incorrect wiring on the 50-amp mini-breaker may leave the circuit unprotected, increasing fire risk.

    Product
    GRAND DESIGN — GRAND DESIGN REFLECTION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V730000·2018-10-16

    Yamaha Recalls SR400 Motorcycles Due to Engine Oil Leak Risk

    Yamaha is recalling 2015-2018 SR400 motorcycles because an engine oil line nut may be loose, causing oil to leak onto the rear tire and increasing crash risk.

    Product
    YAMAHA — YAMAHA SR400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19010·2018-10-16

    Gold Recalls Eddie Bauer Infant Carriers Due to Fall Hazard

    Gold Inc. is recalling Eddie Bauer fabric infant carriers because buckles can break, posing a fall hazard to children. No injuries have been reported.

    Product
    Eddie Bauer fabric infant carriers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V723000·2018-10-15

    Keystone Recalls 2019 Fifth Wheels and Travel Trailers for Axle Bearing Defect

    Keystone RV Company is recalling 2019 Dutchmen, Keystone, and Crossroads fifth wheels and travel trailers because axles may be missing inner bearing races, which can cause bearing failure and affect vehicle handling.

    Product
    DUTCHMEN — DUTCHMEN, KEYSTONE, CROSSROADS AEROLITE, BULLET, COUGAR, PASSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V722000·2018-10-15

    Forest River Recalls School Buses Due to Seat Foam Impact Defect

    Forest River is recalling certain Starcraft and StarTrans school buses because the seat foam may not absorb enough impact in a crash, increasing injury risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS, STARTRANS QUEST, PRODIGY, SENATOR II, QUEST XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V726000·2018-10-15

    Keystone Recalls 2019 Crossroads Fifth Wheels Due to Awning Switch Defect

    Keystone is recalling 2019 Crossroads Cruiser and Volante fifth wheels because defective awning switches may allow the awning to unroll while the vehicle is moving.

    Product
    CROSSROADS — CROSSROADS VOLANTE, CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V724000·2018-10-15

    Mercedes-Benz Recalls 2018 AMG GT Models for Air Bag Software Issue

    Mercedes-Benz is recalling 2018 AMG GT and AMG GT C Cabrio vehicles because a software error may cause both stages of the frontal air bags to deploy in a low-speed crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GT, AMG GT C
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V721000·2018-10-12

    Great Dane Recalls 2019 Everest Trailers for Missing Brake Rollers

    Great Dane is recalling 2019 Everest CL reefer trailers that may lack brake rollers, reducing braking effectiveness and increasing crash risk.

    Product
    GREAT DANE — GREAT DANE EVEREST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V717000·2018-10-12

    Mazda Recalls CX-7, CX-9, and Mazda6 for Air Bag Inflator Defect

    Mazda is recalling 2010-2015 CX-7, CX-9, and Mazda6 vehicles because the front passenger air bag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    MAZDA — MAZDA CX-7, CX-9, MAZDA6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V718000·2018-10-12

    Riverside Dream Trailer Recall for Awning Deployment Risk

    Riverside is recalling one 2018 Dream trailer because the awning may deploy while moving, increasing crash risk. Dealers will replace the awning controller free of charge.

    Product
    RIVERSIDE — RIVERSIDE DREAM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19009·2018-10-11

    Cooper Lighting Recalls Solar-Powered Outdoor LED Fixtures Due to Fire Hazard

    Cooper Lighting is recalling specific All-Pro and Defiant solar-powered outdoor LED light fixtures because the batteries can overheat and cause a fire.

    Product
    All-Pro and Defiant solar-powered outdoor LED light fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V715000·2018-10-11

    Hyundai Recalls 2019 Santa Fe Vehicles Due to Air Bag Bolt Interference

    Hyundai is recalling 2019 Santa Fe vehicles because side curtain air bag mounting bolts may damage the air bags during deployment, increasing injury risk in a crash.

    Product
    HYUNDAI — HYUNDAI SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide