The Recall Desk

State

Northern Mariana Islands product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52176–52200 of 73847

  • HighNHTSA·15V581000·2015-09-21

    Winnebago Recalls 2015-2016 Motorhomes Due to Wiring Fire Risk

    Winnebago is recalling 172 model year 2015-2016 Itasca Sunova and Winnebago Sightseer motorhomes because a wiring harness may be damaged, increasing the risk of fire.

    Product
    ITASCA — ITASCA, ITASCO, WINNEBAGO SUNOVA, SIGHTSEER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowNHTSA·15V579000·2015-09-21

    Mitsubishi Recalls 2011 Outlander Sport for Incorrect Certification Labels

    Mitsubishi is recalling 2011 Outlander Sport vehicles manufactured on December 3, 2010, due to incorrect certification labels lacking the correct VIN. Dealers will install corrected labels free of charge.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V577000·2015-09-18

    Toyota Recalls RAV4 and RAV4 EV for Wiper Linkage Separation Risk

    Toyota is recalling 2009-2012 RAV4 and 2012-2014 RAV4 EV vehicles because water dripping on the wiper joint may cause corrosion and linkage separation, reducing visibility.

    Product
    TOYOTA — TOYOTA RAV4 EV, RAV4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·15245·2015-09-17

    Bed Handles Inc. Recalls Portable Bed Handles Due to Entrapment Hazards

    Bed Handles Inc. is recalling about 113,000 portable bed handles that lack safety retention straps. The missing straps allow the handles to shift, creating gaps that pose a risk of entrapment, strangulation, and death.

    Product
    Portable bed handles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15246·2015-09-17

    The Land of Nod Recalls Mobiles Due to Strangulation Hazard

    The Land of Nod is recalling Follow the Herd mobiles because unraveling yarn poses an entanglement and strangulation risk to young children.

    Product
    Mobiles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15247·2015-09-17

    Zak Designs Recalls 26-Ounce Water Bottles Due to Choking Hazard

    Zak Designs is recalling 26-ounce water bottles sold at Target because the inner plastic straw can break, posing a choking hazard. No injuries have been reported.

    Product
    26-ounce water bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·pha-091715·2015-09-17

    USDA Alerts on Frozen Stuffed Chicken Products Due to Salmonella Contamination

    USDA FSIS issued a public health alert for frozen, raw, stuffed chicken products from Aspen Foods due to confirmed Salmonella Enteritidis contamination.

    Product
    FSIS Issues Public Health Alert For Stuffed Chicken Products Due To Possible Salmonella Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·123-2015·2015-09-16

    Di Stefano Cheese Co. Recalls Parma Ham Produced Without Inspection

    Di Stefano Cheese Co. is recalling approximately 1,280 pounds of Parma Boneless Ham produced in Italy that were not presented for U.S. inspection.

    Product
    Di Stefano Cheese Co. Recalls Ham Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2485-2015·2015-09-16

    Insulet Recalls OmniPod Insulin Devices Due to Deployment Failures

    Insulet Corporation is recalling specific OmniPod insulin devices because they may fail to deploy or retract the cannula, potentially disrupting insulin delivery.

    Product
    OmniPod¿ Insulin Management System. Only the OmniPod¿ device is affected. Catalog Number(s): 14810 (OUS). Intended for subcutaneous delivery of insulin at set and variable rates for the management of diabetes mellitus in persons requiring insulin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2754-2015·2015-09-16

    Intuitive Surgical Recalls da Vinci Si Single-Site Fundus Graspers

    Intuitive Surgical is recalling 6,309 Fundus Graspers used with the da Vinci Si Surgical System because the jaws may become fixed in a closed position.

    Product
    Fundus Grasper; used with the da Vinci Si Surgical System (IS3000); Model numbers: 428058-12, 428058-13. The Intuitive Surgical da Vinci Single-Site Instruments and Accessories used with the da Vinci Si Surgical System (IS3000) are indicated for use by trained physicians in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2484-2015·2015-09-16

    Insulet Recalls OmniPod Insulin Devices Due to Cannula Deployment Failures

    Insulet Corporation is recalling specific OmniPod insulin devices because the cannula may fail to deploy or retract, potentially interrupting insulin delivery.

    Product
    OmniPod¿ Insulin Management System. Only the OmniPod¿ device is affected. Catalog Number(s): POD-ZXP420 (US). Intended for subcutaneous delivery of insulin at set and variable rates for the management of diabetes mellitus in persons requiring insulin.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V576000·2015-09-16

    Forest River Recalls Coachmen Motorhomes Due to Trailer Hitch Bolt Issue

    Forest River is recalling 2011-2016 Coachmen Pursuit, Mirada, and Encounter motorhomes because trailer hitch bolts may not be properly tightened, risking hitch detachment.

    Product
    COACHMEN — COACHMEN MIRADA, ENCOUNTER, PURSUIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2750-2015·2015-09-16

    Intuitive Surgical Recalls da Vinci Si Single-Site Maryland Dissector Instruments

    Intuitive Surgical is recalling 8,217 Maryland Dissector instruments used with the da Vinci Si Surgical System because the jaws may become fixed in a closed position.

    Product
    Maryland Dissector; used with the da Vinci Si Surgical System (IS3000); Model numbers: 428050-12, 428050-13 and 428050-14; The Intuitive Surgical da Vinci Single-Site Instruments and Accessories used with the da Vinci Si Surgical System (IS3000) are indicated for use by…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2752-2015·2015-09-16

    Intuitive Surgical Recalls Cadiere Forceps for da Vinci Si System

    Intuitive Surgical is recalling Cadiere Forceps used with the da Vinci Si Surgical System because the instrument jaws may become fixed in a closed position.

    Product
    Cadiere Forceps; used with the da Vinci Si Surgical System (IS3000); Model numbers: 428055-12, 428055-13. The Intuitive Surgical da Vinci Single-Site Instruments and Accessories used with the da Vinci Si Surgical System (IS3000) are indicated for use by trained physicians…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2742-2015·2015-09-16

    Terumo CDI 500 Blood Parameter Monitoring System Recalled for Inaccurate Readings

    Terumo is recalling 4,638 CDI 500 Blood Parameter Monitoring Systems worldwide due to inaccurate readings of vital blood parameters following a software upgrade to version 1.69.

    Product
    CDI 500 Blood Parameter Monitoring System. Provides continuous, on-line monitoring of the extracorporeal partial pressure of oxygen and and carbon dioxide, pH, potassium, oxygen saturation, hematocrit, hemoglobin and temperature.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1417-2015·2015-09-16

    3M Recalls DuraPrep Surgical Solution Due to Chemical Contamination

    3M is recalling DuraPrep Surgical Solution because the product may be contaminated with a toxic compound.

    Product
    DuraPrep Surgical Solution Iodine Povacrylex (0.7% Available Iodine) and Isopropyl Alcohol (74% w/w) Patient Preoperative Skin Preparation, supplied in a) 0.9 fl oz, 26 mL Single Use Applicator w/urethane sponge and 2-count Cotton-tipped swabs per pouch, packaged in 20 pouches…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2746-2015·2015-09-16

    Smith & Nephew Birmingham Hip Resurfacing Acetabular Cup Recalled

    Smith & Nephew is recalling specific Birmingham Hip Resurfacing Acetabular Cups because the system's revision rates were higher than established benchmarks.

    Product
    Smith & Nephew BIRMINGHAM HIP (TM) RESURFACING ACETABULAR CUP W/IMPACTOR, REF Numbers: 74120144 (44 MM), 74120146 (46 MM), 74122146 (46 MM), 74122148 (48 MM), 74120148 (48 MM), 74120150 (50 MM), 74122150 (50 MM), 74122152 (52 MM), 74120152 (52 MM), 74120154 (54 MM) Product…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2735-2015·2015-09-16

    Medtronic Hemocor Hemoconcentrators Recalled for Low Ultrafiltration Performance

    Medtronic Perfusion Systems is recalling Hemocor Hemoconcentrators because they demonstrate low ultrafiltration performance below product specifications.

    Product
    MEDIVATORS HEMOCOR HPH700, HPH-1400TS, HPH-1000TS. Enables the perfusionist to manage the patient's hematocrit and fluid status.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2758-2015·2015-09-16

    Intuitive Surgical Recalls Fenestrated Bipolar Forceps for da Vinci System

    Intuitive Surgical is recalling 21,684 Fenestrated Bipolar Forceps used with the da Vinci Si Surgical System because the jaws may become fixed in a closed position.

    Product
    Fenestrated Bipolar Forceps; used with the da Vinci Si Surgical System (IS3000); Model numbers: 428093-12, 428093-13. The Intuitive Surgical da Vinci Single-Site Instruments and Accessories used with the da Vinci Si Surgical System (IS3000) are indicated for use by trained…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V575000·2015-09-16

    Vermeer Recalls Brush Chippers and Stump Cutters for Missing Reflectors

    Vermeer is recalling specific brush chippers and stump cutters because their LED side marker lights lack required reflectors, reducing vehicle visibility.

    Product
    VERMEER — VERMEER BC1800XL, BC600XL, SC802, SC602
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2753-2015·2015-09-16

    Intuitive Surgical Recalls da Vinci Si Single-Site Needle Drivers

    Intuitive Surgical is recalling 89 da Vinci Si Single-Site Needle Drivers because the jaws may become fixed in a closed position.

    Product
    Needle Driver; used with the da Vinci Si Surgical System (IS3000); Model numbers: 428056-12, 428056-13. The Intuitive Surgical da Vinci Single-Site Instruments and Accessories used with the da Vinci Si Surgical System (IS3000) are indicated for use by trained physicians in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2757-2015·2015-09-16

    Intuitive Surgical Recalls Curved Needle Drivers for da Vinci System

    Intuitive Surgical is recalling 3,698 Curved Needle Drivers used with the da Vinci Si Surgical System because the jaws may become fixed in a closed position.

    Product
    Curved Needle Driver; used with the da Vinci Si Surgical System (IS3000); Model numbers: 428088-12, 428088-13. The Intuitive Surgical da Vinci Single-Site Instruments and Accessories used with the da Vinci Si Surgical System (IS3000) are indicated for use by trained…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2751-2015·2015-09-16

    Intuitive Surgical Recalls da Vinci Si Single-Site Clip Appliers

    Intuitive Surgical is recalling 17,617 da Vinci Si Single-Site Clip Appliers because the jaws may become fixed in a closed position during use.

    Product
    Medium -Large Clip Applier; used with the da Vinci Si Surgical System (IS3000); Model numbers: 428053-12, 428053-15. The Intuitive Surgical da Vinci Single-Site Instruments and Accessories used with the da Vinci Si Surgical System (IS3000) are indicated for use by trained…
    Category
    Medical Device
    Distribution
    Distributed nationwide