The Recall Desk

State

Northern Mariana Islands product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38826–38850 of 73764

  • SevereNHTSA·18V254000·2018-04-19

    Thomas Built Buses Recall Wall-Mounted Seats Due to Crash Risk

    Daimler Trucks North America is recalling 2014-2018 Thomas Built Buses because wall-mounted seat brackets may crack, increasing injury risk in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER EFX, SAF-T-LINER HDX, MINOTOUR, SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V250000·2018-04-19

    Daimler Recalls 2018-2019 Thomas Built Buses Saf-T-Liner C2 for Fire Risk

    Daimler Trucks North America is recalling 2018-2019 Thomas Built Buses Saf-T-Liner C2 transit buses because a battery cable may rub against a bracket, increasing the risk of a fire.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18143·2018-04-19

    Petit Collage Wooden Toy Xylophones Recalled for Choking Hazard

    Wild & Wolf is recalling Petit Collage wooden toy xylophones because the beater stick ball can detach, posing a choking risk to young children.

    Product
    Petit Collage musical jumbo wooden xylophones
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V252000·2018-04-19

    GM Recalls 2018 Chevrolet Equinox for Improperly Tempered Door Glass

    General Motors is recalling 2018 Chevrolet Equinox vehicles because the front door window glass may not be properly tempered, increasing injury risk if broken.

    Product
    CHEVROLET — CHEVROLET EQUINOX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18T004000·2018-04-19

    Kumho Recalls Solus KH16 Tires Due to Belt Separation Risk

    Kumho is recalling specific Solus KH16 tires because the belts may separate under severe conditions, increasing the risk of a crash.

    Product
    TIRES recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V253000·2018-04-19

    Thomas Built Buses Recall School Buses Due to Seat Bracket Defect

    Daimler Trucks North America is recalling 2014-2018 Thomas Built Buses school buses because a wall mounting bracket may crack, increasing injury risk in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX, SAF-T-LINER C2, SAF-T-LINER EFX, MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V248000·2018-04-18

    BMW Recalls Vehicles for Electric Water Pump Fire Risk

    BMW is recalling 2007-2012 models because a failing electric auxiliary water pump can overheat the circuit board, increasing the risk of a fire.

    Product
    MINI — MINI, BMW, ROLLS-ROYCE COOPER S CLUBMAN, COOPER S CONVERTIBLE, X6 ACTIVEHYBRID SAC, X6 M
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1365-2018·2018-04-18

    Fresenius Liberty Select Cycler Recalled for Software Overfill Risk

    Fresenius Medical Care is recalling Liberty Select Cyclers due to a software issue that may cause overfill, posing a risk of serious injury or death.

    Product
    Liberty Select Cycler (SW v.2.8.7), Material Number RTLR108343 Product Usage: The device is indicated for acute and chronic peritoneal dialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V247000·2018-04-18

    Volkswagen Recalls 2006-2007 Passat Vehicles Due to Air Bag Inflator Defect

    Volkswagen is recalling 2006-2007 Passat sedans and wagons because the driver's air bag inflator may explode during deployment, posing a risk of serious injury or death.

    Product
    VOLKSWAGEN — VOLKSWAGEN PASSAT, PASSAT WAGON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1351-2018·2018-04-18

    W & H DentalWerk Recalls S-N1 and S-N2 Foot Controls

    W & H DentalWerk is recalling S-N1 and S-N2 foot controls because they may fail to stop the motor, posing a risk of serious patient injury.

    Product
    Foot Controls Model: S-N1 and S-N2 Product Usage: Variable foot control for use with drive units operating mechanical instruments.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1318-2018·2018-04-18

    Reliance Medical Products Recalls Refractor Suspension Arms Due to Missing Parts

    Reliance Medical Products is recalling 933 Refractor Suspension Arms because missing parts caused the device to fall on a patient.

    Product
    Refractor Suspension Arm (P/N: 525004, 05 and 525006, 07) The Intended use of this medical device, as part of system to store and position ophthalmological examination and diagnostic equipment, is to store and position for examination a device commonly known as a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1141-2018·2018-04-18

    Poppies International Recalls Belgian Mini Eclairs Due to Listeria Risk

    Poppies International is recalling three brands of frozen Belgian mini eclairs because they may be contaminated with Listeria monocytogenes.

    Product
    GFS Belgian Mini Chocolate Topped Eclairs, Keep Frozen, Net Wt . 700 g.; Signature Select Belgian Style Mini Eclairs, Keep Frozen, 420 g; Delizza Patisserie Belgian Custard Cream Mini Eclairs, 420 g.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1344-2018·2018-04-18

    ICU Medical Recalls 7-inch Intravascular Administration Sets with Incorrect Spin Collar

    ICU Medical is recalling 250 pouches of 7-inch intravascular administration sets because they were manufactured with an incorrect spin collar.

    Product
    7" Ext Set w/MicroClave¿, Clave¿ T-Connector, Clamp, Rotating Luer, 50 pouches per case, Item AH7262. The firm name on the label is icumedical, San Clemente, CA. The Intravascular Administration Set is a single use, sterile, non-pyrogenic device which provides access for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1367-2018·2018-04-18

    Teleflex Medical Recalls Latex Rebreathing Bags Due to Missing Allergen Warning

    Teleflex Medical Europe Ltd is recalling 107,962 latex rebreathing bags because they lack the required warning that the product contains natural rubber latex, which may cause allergic reactions.

    Product
    Latex Rebreathing Bags: Product Code Equivalent Code (a) 151174050 151174 (b) 153000005 153000005 (c) 153000010 153000010 (d) 153000020 153000020 (e) 153000030 153000030 (f) 153000050 153000050 (g) 210700050 2107050 (h) 210700102 2107102 (I) 210700202 2107202 (j)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1356-2018·2018-04-18

    Bard Feeding Tubes Recalled for Ineffective Connector Fusion

    C.R. Bard is recalling specific lots of Bard Adult/Pediatric Feeding Tubes because the tubing and ENFit connector may not be fused effectively.

    Product
    Bard(R) Adult/Pediatric Feeding Tube, ENFit(TM), REF EN0036420 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18V245000·2018-04-18

    Newmar Recalls Motorhomes Due to Headlight Beam Switching Defect

    Newmar is recalling specific 2013-2017 motorhomes because low beam headlights turn off when high beams are activated, reducing driver visibility.

    Product
    NEWMAR — NEWMAR LONDON AIRE, DUTCH STAR, VENTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1349-2018·2018-04-18

    Getinge Recalls VOLISTA StandOP Surgical Lights Due to Handle Detachment Risk

    Getinge is recalling 5,214 VOLISTA StandOP surgical lights because the central handle holder can detach, potentially dropping particles into the sterile field during procedures.

    Product
    VOLISTA StandOP Surgical Light; Model numbers VLT600 SF AIM STP, VLT600 DF AIM STP, Ref. codes ARD568811901, ARD568811911 ARD568811951, ARD568811961 The device is designed to illuminate the body of a patient during surgical operations, diagnostics and treatment. These…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1355-2018·2018-04-18

    Bard Infant Feeding Tube Recalled for Ineffective Connector Fusion

    C.R. Bard is recalling 23,400 infant feeding tubes because the tubing and connector may not be effectively fused.

    Product
    Bard(R) Infant Feeding Tube, ENFit(TM), REF EN0036410 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term tube…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1341-2018·2018-04-18

    Beckman Coulter AQUIOS CL Flow Cytometer System Recalled for Sample ID Errors

    Beckman Coulter is recalling 288 AQUIOS CL Flow Cytometer Systems because the single tube loader may process the same sample with two different IDs, potentially causing erroneous results.

    Product
    AQUIOS CL Flow Cytometer System, Catalog #B30166. The AQUIOS CL Flow Cytometer system is an automated analyzer that use a no-wash sample preparation process.The firm name on the label is Beckman Coulter Ireland, Inc., Co. Clare, Ireland.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·18142·2018-04-18

    Primark Recalls Decorative Cushions Due to Fire Hazard

    Primark is recalling about 14,500 decorative cushions sold in the northeastern U.S. because they can catch fire if exposed to an ignition source.

    Product
    Decorative cushions
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1319-2018·2018-04-18

    Hill-Rom Progressa Bed Recall Due to Brake Component Failure Risk

    Hill-Rom is recalling 2,117 Progressa adjustable hospital beds because a braking system component may break, causing unwanted bed movement and potential injury.

    Product
    Progressa Bed - AC-powered adjustable hospital bed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18V246000·2018-04-18

    Riverside Recalls 2015-2017 Motorhomes Due to Fire Extinguisher Defects

    Riverside RV is recalling 2015-2017 White Water, Water Fall, and Mt. McKinley motorhomes because certain fire extinguishers may clog or detach, posing injury risks.

    Product
    RIVERSIDE — RIVERSIDE WATER FALL, MT. MCKINLEY, WHITEWATER
    Category
    Vehicle
    Distribution
    Distributed nationwide