The Recall Desk

State

Northern Mariana Islands product recalls

73,363 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
8
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 8 (35%) are Severe.

Which agencies issued them

These figures cover only the 23 recalls whose distribution notice names Northern Mariana Islands specifically. The 73,363 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18376–18400 of 73386

  • HighNHTSA·22V827000·2022-11-03

    2021 Cadillac Escalade daytime running lights control software defect

    General Motors is recalling 2021 Cadillac Escalade vehicles. The daytime running lights may not deactivate when headlights are on, which may cause glare and reduce visibility, increasing crash risk.

    Product
    CADILLAC — CADILLAC, CHEVROLET, GMC ESCALADE, ESCALADE ESV, SUBURBAN, YUKON XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23707·2022-11-03

    BS Interactive Stashables Finger Skateboard Ramp Sets Lead Paint Hazard

    BS Interactive is recalling Stashables Finger Skateboard Ramp Sets because the miniature skateboards and scooters contain lead paint levels exceeding federal limits and fail lead content bans, posing a lead poisoning risk to young children.

    Product
    Stashables Finger Skateboard Ramp Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23708·2022-11-03

    Myx Connected Exercise Bicycles Recalled for Pedal Detachment Risk

    Myx is recalling approximately 162,000 MYX I, MYX II, and MYX II Plus exercise bicycles because pedals can loosen or detach during use, causing injury. Myx has received 864 reports of pedal loosening or detachment, including 75 injury reports involving bruises and cuts.

    Product
    MYX I, MYX II and MYX II Plus Connected Exercise Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23031·2022-11-03

    Bolt Foldable Children's Scooters Recalled for Excessive Lead Paint

    Anker Play Products is recalling about 5,000 Bolt Foldable Children's Scooters sold at discount stores from March through May 2022. The paint contains lead levels exceeding the federal ban, creating a lead poisoning hazard for young children.

    Product
    Bolt Foldable Children's Scooters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V826000·2022-11-03

    Micro Bird Recalls School Buses Due to Incorrectly Attached Rub Rails

    Micro Bird is recalling 2021-2023 G5, 2022-2023 MB II, and 2022 T-Series school buses because seat-level rub rails may be incorrectly attached, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS, MB II SCHOOL BUS, T-SERIES SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23033·2022-11-03

    Tangame Busy Toy Houses Recalled for Lead Paint and Phthalate Violations

    Tangame Busy Houses, wooden activity toy cubes sold on Amazon, contain lead paint on a zipper, lead in a plastic phone cord, and phthalates in a horn bulb, exceeding federal safety bans. No injuries have been reported.

    Product
    Tangame Busy Houses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23709·2022-11-03

    Rad Power Bikes RadWagon 4 Electric Cargo Bikes Recall

    Rad Power Bikes is recalling about 29,300 RadWagon 4 electric cargo bikes because the tires can unexpectedly go flat or separate, risking falls and crashes. The firm has received 137 reports of tire failures and eight injury reports.

    Product
    RadWagon 4 Electric Cargo Bikes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0019-2023·2022-11-02

    Atenolol 25mg bottles mislabeled; contain Clopidogrel 75mg tablets

    Golden State Medical Supply Inc. is recalling 2,584 bottles of Atenolol 25mg tablets nationwide. Bottles labeled as Atenolol 25mg actually contain Clopidogrel 75mg tablets—a different medication.

    Product
    ATENOLOL — ATENOLOL (ATENOLOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0023-2023·2022-11-02

    Sodium Bicarbonate Injection Recalled for Defective Vials and Glass Breakage

    Nationwide recall of 8.4% sodium bicarbonate injection vials due to container defects causing vial breakage and glass fragments when pressurized during preparation.

    Product
    8.4% Sodium Bicarbonate Injection, USP 50 mEq/50 mL (1 mEq/mL) 50 mL Single Dose Vials, packaged in cartons of 20 vials, Rx Only, Mfd for: Civica, Inc. Lehi, Utah 84043, Mfd by: Exela Pharma Sciences, LLC, Lenoir, NC 28645, Carton NDC 72572-740-20, vial NDC 72572-740-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V824000·2022-11-02

    Quality Trailers Ohio Recalls 2022 Trailers Due to Coupler Welding Defect

    Quality Trailers Ohio is recalling 2022 A, AW, B, and DH trailers because improperly welded couplers may cause the trailer to separate from the tow vehicle.

    Product
    QUALITY TRAILERS OHIO — QUALITY TRAILERS OHIO TANDEM B, ECONOMY SERIES DH, AW, A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0022-2023·2022-11-02

    Sodium Bicarbonate Injection Recalled for Defective Vials with Glass Breakage Risk

    Exela Pharma Sciences is recalling 2,123,040 vials of Sodium Bicarbonate 8.4% Injection due to container defects causing vial breakage and glass release when pressurized during product preparation.

    Product
    SODIUM BICARBONATE — SODIUM BICARBONATE (SODIUM BICARBONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0124-2023·2022-11-02

    Medline Pre-Op CHG Bathing Kit recalled for incorrect expiration dates

    Medline is recalling 460 Pre-Op CHG Bathing Kits because the CHG solution and blood culture bottles have expiration dates that don't match the kit label. Expired components could compromise effectiveness.

    Product
    MEDLINE PRE-OP CHG BATHING KIT Reorder #: P164756
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V823000·2022-11-02

    2022 Audi and Volkswagen vehicles recalled for blank rearview cameras

    Certain 2022 Audi and Volkswagen vehicles have a defective rearview camera that may go blank or unresponsive, reducing rear visibility. Dealers will replace the camera for free.

    Product
    AUDI — AUDI, VOLKSWAGEN RS 3, GTI, ID.4, Q4 E-TRON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0122-2023·2022-11-02

    Medline Blood Culture Kits recalled due to mismatched component expiration dates

    Medline Industries is recalling 1,600 blood culture kits (Reorder # DYNDH1592) because component expiration dates don't match the kit label. Affected components include CHG Solution and Bactec bottle plastic.

    Product
    MEDLINE BLOOD CLUTURE KIT, Reorder #: DYNDH1592
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0119-2023·2022-11-02

    ARTIS pheno interventional x-ray system software defect prevents treatment continuation

    Siemens is recalling ARTIS pheno x-ray systems with VE10B software due to three potential software issues that may prevent continued treatment on the affected system, potentially requiring use of an alternate system.

    Product
    ARTIS pheno, Interventional fluoroscopic x-ray system, Model No. 10849000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0140-2023·2022-11-02

    Stryker INBONE Tibial Tray recalled for oversized lock detail defect

    Wright Medical Technology is recalling one Stryker INBONE Tibial Tray due to an oversized tibial tray lock detail that exceeds product specifications and could affect device functionality.

    Product
    Stryker INBONE Tibial Tray, Left Plasma Spray Ti6Al4V, CPti, Use w/ 18mm Stem Base, REF 200252904, Size 4
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0021-2023·2022-11-02

    Quinapril and Hydrochlorothiazide Tablets Recalled Due to Manufacturing Impurity

    Aurobindo Pharma USA Inc. is recalling Quinapril/Hydrochlorothiazide Tablets 20mg/12.5mg due to N-nitroso-quinapril impurity above acceptable limits from manufacturing deviations. Affected lots QE2021005-A and QE2021010-A were distributed nationwide.

    Product
    QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE — QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE (QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0128-2023·2022-11-02

    ConvaTec Esteem+ Durahesive Plus Ostomy Pouch Release Liner Defect

    ConvaTec recalled 182 units of Esteem+ Durahesive Plus ostomy pouches nationwide due to impaired release liner functionality. The defect affects pouches with batch number 2A02671 and UDI 768455115334.

    Product
    ConvaTec Esteem+ Durahesive Plus, Drainable Pouch, 3/4-2 1/4 in., 19-64mm, REF 416975. For the management of stoma output following a colostomy or ileostomy procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22E093000·2022-11-02

    ITR Recalls Oasis Chinook Hydronic Heaters Due to Fuel Line Defect

    International Thermal Research is recalling Oasis Chinook Hydronic Heaters because an air line may be installed instead of a fuel line, creating a fire risk.

    Product
    FUEL SYSTEM, DIESEL:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V858000·2022-11-02

    2021 Volkswagen ID.4 Passenger Air Bag May Fail to Deploy Properly

    Volkswagen is recalling certain 2021 ID.4 vehicles because the passenger air bag may be incorrectly folded and could fail to protect occupants during a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID.4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0130-2023·2022-11-02

    ConvaTec Ostomy Pouch Recalled for Impaired Release Liner Functionality

    ConvaTec is recalling 2,611 units of its Active Life ostomy pouch due to impaired release liner functionality. The defect may affect product performance and seal integrity.

    Product
    ConvaTec Active Life, One-Piece Drainable Pouch, 3/4-2 1/2 in., 19-64mm, REF 400599. For the management of stoma output following a colostomy or ileostomy procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0127-2023·2022-11-02

    ConvaTec Esteem+ Durahesive Plus ostomy pouches recalled for release liner defect

    ConvaTec is recalling 5,284 units of Esteem+ Durahesive Plus ostomy pouches due to impaired release liner functionality. The defect may affect proper device operation for patients managing colostomy or ileostomy output.

    Product
    ConvaTec Esteem+ Durahesive Plus, Drainable Pouch, 3/4-2 1/2 in., 19-64mm, REF 416976. For the management of stoma output following a colostomy or ileostomy procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide