The Recall Desk

State

Northern Mariana Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55201–55225 of 73850

  • SevereNHTSA·15V111000·2015-02-25

    McNeilus Recalls Bridgemaster V Mixers Due to Parking Brake Defect

    McNeilus is recalling 2005-2014 Bridgemaster V Mixers because the optional parking brake system may fail to maintain required pressure, increasing crash risk.

    Product
    MCNEILUS — MCNEILUS BRIDGEMASTER V MIXER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1128-2015·2015-02-25

    Mako Surgical Recalls Restoris Partial Knee Application RIO Due to Burr Malfunction

    Mako Surgical Corporation is recalling 228 units of the Restoris Partial Knee Application RIO because the surgical burr may continue spinning outside the intended boundary after controls are released.

    Product
    Restoris Partial Knee Application (PKA) RIO (TGS 2.0). For use with the Robotic Arm Interactive Orthopedic System (RIO), is indicated for use in surgical knee procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0391-2015·2015-02-25

    Hospira Recalls Lidocaine Hydrochloride Injection Due to Particulate Matter

    Hospira is recalling specific vials of 1% Lidocaine Hydrochloride Injection because a returned sample contained human hair attached to the stopper.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1126-2015·2015-02-25

    CME America Recalls BodyGuard 323 Infusion Pumps for Over-Delivery Risk

    CME America is recalling BodyGuard and BodyGuard 323 infusion pumps due to a potential for over-delivery of medication.

    Product
    BodyGuard 323 pump, models 100-510PXSI, 100-516PXS, 100-517PXS, 100-518PXS, 100-603XSA and 100-603XSAP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1224-2015·2015-02-25

    Probar Recalls Frosted Peanut Butter Bars for Undeclared Milk Allergen

    Probar LLC is voluntarily recalling specific lots of Frosted Peanut Butter BASE Protein Bars due to the possible presence of an undeclared milk allergen.

    Product
    PROBAR Frosted Peanut Butter BASE Protein Bar, 2.46 oz film wrapped bar packaged in 12 wrapped units per sleeve/carton. Unit UPC:8-53152-10060-5. 12 count box UPC: 8-53152-10061-2.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1127-2015·2015-02-25

    Nidek MC-500 Laser Photocoagulator Recalled for Spot Size Control Defect

    Nidek Inc is recalling 16 MC-500 Multicolor Laser Photocoagulators because the spot size control may turn by itself, posing a risk of unintended laser delivery.

    Product
    MC-500 Multicolor Laser Photocoagulator; Indicated for use in retinal photocoagulation for treatment of ocular fundus diseases like diabetic retinopathy, age-related macular degeneration, retinopathy of prematurity and retinal detachment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V112000·2015-02-25

    Farber Specialty Vehicles Recalls Wheelchair Lifts Due to Cracking Risk

    Farber Specialty Vehicles is recalling specialty vehicles equipped with Ricon wheelchair lifts because the platform side plates may crack, posing a risk of injury.

    Product
    WINNEBAGO — WINNEBAGO, FREIGHTLINER, FORD WFJ33S, MBC, XCS, F-550 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1116-2015·2015-02-25

    Terumo HX2 Temperature Management System Recalled for Valve Malfunction

    Terumo is recalling 103 HX2 Temperature Management Systems because a malfunctioning mixing valve can cause loss of cooling or heating capability during surgery.

    Product
    Terumo HX2 Temperature Management System provides temperature control of two independent water circuits that directly controls the temperature of patient blood and cardioplegia solution during cardiovascular surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1124-2015·2015-02-25

    Teleflex Recalls RUSCH Endotracheal Tubes for Cuff Diameter Labeling Error

    Teleflex is recalling RUSCH Curved Reinforced Endotracheal Tubes because the labeled cuff diameter does not match the actual cuff diameter, though the actual product meets specifications.

    Product
    R¿SCH Curved Reinforced Endotracheal Tube: Rusch Reinforced Endotracheal Tube is designated for oral or nasal intubation and are indicated for airway management. The product may be used to reduce the potential for kinking whenever an unusual positioning of the head or neck is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0387-2015·2015-02-25

    Hospira Recalls Vancomycin Hydrochloride Injection Due to Temperature Abuse

    Hospira Inc. is recalling specific lots of Vancomycin Hydrochloride for Injection because they experienced uncontrolled temperature excursions during transit.

    Product
    VANCOMYCIN HYDROCHLORIDE — VANCOMYCIN HYDROCHLORIDE (VANCOMYCIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1129-2015·2015-02-25

    Cincinnati Sub-Zero CT-99 Cold Therapy Pad Recall for Seal Separation

    Cincinnati Sub-Zero is recalling CT-99 cold therapy pads because seals may separate during use, causing water leaks.

    Product
    Cold Therapy Pad - cold water circulating pad, one unit per package. The pads are used to provide a patient with local cold therapy by circulating chilled water through the pad that has been positioned on the patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1121-2015·2015-02-25

    Pulsiocath PiCCO ProAQT Monitoring Kit Recalled for Packaging Defects

    Pulsion Medical Inc is recalling 90 units of the Pulsiocath PiCCO ProAQT Monitoring Kit due to cracks and holes found in the primary packaging.

    Product
    Pulsiocath PiCCO ProAQT Monitoring Kit, single-use cardiac output (CO) sensor, one unit per plastic sterilizable package. Product Usage: Measures cardiac output by the thermodilution method, measurement of arterial blood pressure, and for cardiac output determination by…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0388-2015·2015-02-25

    Hospira Recalls Ketorolac Tromethamine Injections Due to Temperature Abuse

    Hospira Inc. is recalling 100 vials of Ketorolac Tromethamine Injection due to uncontrolled temperature excursions during transit. The product was limited to one shipment to a distributor.

    Product
    KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1119-2015·2015-02-25

    Siemens Artis One Angiography System Recalled for Monitor Failure

    Siemens Medical Solutions is recalling one Artis One angiography system because the monitor may fail and require a power cycle to resume operation.

    Product
    Artis One; The Artis One is an angiography system developed for diagnostic interventional procedures including, but not limited to pediatric and obese patients. Procedures that can be performed with the Artis One include cardiac angiography, neuro-angiography, general…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0390-2015·2015-02-25

    Hospira Recalls Vancomycin Hydrochloride Injection Due to Temperature Excursions

    Hospira Inc. is recalling 90,600 vials of Vancomycin Hydrochloride for Injection because the products experienced uncontrolled temperature excursions during transit.

    Product
    VANCOMYCIN HYDROCHLORIDE — VANCOMYCIN HYDROCHLORIDE (VANCOMYCIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15T007000·2015-02-24

    Alliance Tires Recalled for Tread Separation Risk

    Alliance Tire Americas is recalling specific model 396 tires because the tread may separate, potentially causing a rapid loss of air and increasing the risk of a crash.

    Product
    TIRES:TREAD/BELT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15721·2015-02-24

    Safe Step Walk-In Tubs Recalled Due to Heated Seat Burn Hazard

    Oliver Fiberglass and NuWhirl Systems are recalling about 6,400 Safe Step walk-in tubs because the heated seat can get stuck on and overheat, posing a burn risk.

    Product
    Safe Step Walk-In Tubs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·15V107000·2015-02-24

    Prevost Recalls 2014 X3-45 Coaches Due to Seat Belt Defect

    Prevost is recalling 38 model year 2014 X3-45 commuter coaches because the driver's seat belt retractor may not lock properly, increasing injury risk in a crash.

    Product
    PREVOST — PREVOST X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide