The Recall Desk

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.

24126–24150 of 73518

  • HighFDA (Devices)·Z-2103-2021·2021-07-28

    Knee Prosthesis Recall: Packaging Mixup May Cause Wrong Size Implantation

    Encore Medical recalls DJO Surgical EMPOWR 3D knee prosthetic components because packaging labels may not match the product inside, risking implantation of incorrect prosthesis sizes.

    Product
    DJO Surgical EMPOWR 3D Knee Tibial Insert - e-plus, REF: 341-12-711, Left Sz. 11 12mm, CE0086, Sterile H2O2, UDI: (01)00888912166980
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2100-2021·2021-07-28

    Cortoss Bone Augmentation Material Recalled Due to Storage Temperature Excursion

    Stryker Spine is recalling 559 units of Cortoss Bone Augmentation Material 5cc Cartridges due to a 12-hour temperature excursion at the distribution center. The affected lot may not meet required storage conditions.

    Product
    Cortoss Bone Augmentation Material 5cc Cartridge, Catalog Number 2101-0005, GTIN 00808232000962
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2133-2021·2021-07-28

    Hip implant acetabular liners recalled for edge-loading and premature wear

    Exactech Connexion GXL acetabular polyethylene liners for hip implants are recalled due to risk of edge-loading and premature wear in certain patient configurations and implant positions. Approximately 89,050 units distributed nationwide are affected.

    Product
    Exactech Connexion GXL acetabular polyethylene liners used in the following systems: Catalog numbers 132-32-XX, Acumatch GXL 15 Degree Liner, 32mm; Novation GXL Liner, Lipped Ant, 32mm; and Novation GXL Liner, Lipped, 32mm. Orthopedic hip implant component.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0689-2021·2021-07-28

    Erythromycin Topical Solution 2% Recalled for Failed Impurities Specifications

    Teligent Pharma, Inc. is recalling Erythromycin Topical Solution USP 2% (60 mL, Lot 14180) distributed nationwide because it failed impurities and degradation specifications.

    Product
    Erythromycin Topical Solution USP, 2% 60 mL, Rx Only, Teligent Pharma, Inc., Buena, NJ 08310, NDC 52565-027-59
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2108-2021·2021-07-28

    Mindray battery cradle may prevent monitor from powering on

    Mindray is recalling the 3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60 and TM80 Telepack physiological monitors. The cradle may prevent the monitor from powering on. Approximately 804 units were distributed in the US and Canada.

    Product
    3AA battery cradle (Part Number 045-001699-01) used with BeneVision TD60 Telepack (Model Number 115-047566-00 /115-060044-00) and TM80 Telepack (Model Number 115-047565-00 / 120-018867-00). Used with physiological data monitor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0690-2021·2021-07-28

    Erythromycin Topical Gel 2% Recalled Due to Failed Impurity Specifications

    Teligent Pharma, Inc. is recalling Erythromycin Topical Gel 2% due to failed impurities and degradation specifications. The recall affects approximately 22,824 tubes distributed nationwide.

    Product
    Erythromycin Topical Gel, 2%, Net Wt. (a) 30 g,(NDC 52565-033-30) (b) 60 g,(NDC 52565-033-60) Rx Only, Manufactured by: Teligent Pharma, Inc. , Buena, NJ 08310,
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V574000·2021-07-27

    Mack Recalls 2022 MD Trucks Due to Loose Front Suspension Bolts

    Mack Trucks is recalling 2022 MD trucks because loose front suspension bolts may detach, potentially causing loss of vehicle control and increasing crash risk.

    Product
    MACK — MACK MD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V573000·2021-07-27

    Mack Trucks Recalls 2021 LR, Granite, and TE Models for Brake Defect

    Mack Trucks is recalling 2021 LR, Granite, and TE vehicles because incorrect rear brake cams may cause inoperative rear axle brakes, increasing crash risk.

    Product
    MACK — MACK LR, GRANITE (GR), TE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21768·2021-07-27

    Oculus Quest 2 Removable Foam Facial Interfaces Due to Skin Irritation Risk

    Facebook Technologies is recalling about 4 million removable foam facial interfaces for Oculus Quest 2 virtual reality headsets because the foam can cause facial skin irritation and reactions. Consumers should stop using affected interfaces and contact the manufacturer for a free silicone replacement.

    Product
    Removable Foam Facial Interfaces for Oculus Quest 2 Virtual Reality Headsets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V571000·2021-07-27

    Newmar Recreational Vehicles Recalled for Window Adhesive Failure

    Newmar is recalling select 2018-2021 recreational vehicles due to potential window adhesive failure. The vent portion of affected windows may detach, increasing crash and injury risk.

    Product
    NEWMAR — NEWMAR NEW AIRE, LONDON AIRE, ESSEX, VENTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V568000·2021-07-26

    Eclipse Recalls 2020-2021 Trailers Due to Gas Leak Risk

    Eclipse is recalling 2020-2021 Attitude, Stellar, and Iconic trailers because a stove bolt may be overtightened, damaging the seal and causing a gas leak.

    Product
    ECLIPSE — ECLIPSE ATTITUDE, ICONIC, STELLAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V566000·2021-07-26

    2021–2022 Spartan K2 RV Chassis Fuel Leak Recall

    Shyft Group is recalling certain 2021–2022 Spartan K2 RV Chassis vehicles with Cummins L9 Diesel Engines due to fuel leaks from pressurized hoses. The leak may increase fire risk if an ignition source is present.

    Product
    SPARTAN — SPARTAN K2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V567000·2021-07-26

    Marion Body Works Recalls Spartan Fire Emergency Vehicles for Pump Defect

    Marion Body Works is recalling 2009-2021 Spartan Fire Gladiator and MetroStar emergency vehicles because a corroded solenoid may cause loss of water pressure.

    Product
    SPARTAN FIRE — SPARTAN FIRE GLADIATOR, METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V569000·2021-07-26

    2021 Audi E-Tron recalled for brake booster defect

    Volkswagen is recalling certain 2021 Audi E-Tron models due to improperly welded brake boosters that may separate, reducing braking assistance and stability control.

    Product
    AUDI — AUDI E-TRON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V565000·2021-07-23

    Autocar Recalls 2022 Xpeditor Trucks Due to Fuel Hose Leak Risk

    Autocar is recalling 2022 Xpeditor vehicles with specific diesel engines because a fuel hose may leak, increasing the risk of fire.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21E067000·2021-07-23

    Terran Axle Trailer Axles Recalled for Improperly Tightened Spindle Nuts

    Terran Axle LLC is recalling Trailer Axles part number 020401 because improperly tightened spindle nuts may cause excessive vibration and overheating, increasing the risk of a crash.

    Product
    SUSPENSION:MULTIPLE AXLE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V560000·2021-07-23

    GM Recalls 2017-2019 Chevrolet Bolt EVs for Battery Fire Risk

    General Motors is recalling 2017-2019 Chevrolet Bolt EVs because the high-voltage battery may catch fire when fully charged, increasing injury risk.

    Product
    CHEVROLET — CHEVROLET BOLT EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E068000·2021-07-23

    Ricon Baylift Wheelchair Lift Recall for Barrier Strength Defect

    Ricon is recalling Baylift Wheelchair Lifts because the outer barrier may fail to withstand maximum force, increasing injury risk.

    Product
    EQUIPMENT ADAPTIVE/MOBILITY:WHEELCHAIR LIFT/RAMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·21764·2021-07-22

    Bel Furniture Recalls Barrington 5-Drawer Chests for Tip-Over Hazards

    Bel Furniture is recalling about 90 Barrington 5-Drawer Chests because the dressers can tip over and trap children if not anchored to the wall. One child has already been injured when a chest tipped over.

    Product
    Barrington 5-Drawer Chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide