The Recall Desk

State

Northern Mariana Islands product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

45101–45125 of 73832

  • ModerateFDA (Devices)·Z-0730-2017·2016-12-21

    Merge Cardio software recall for data loss during inactivity

    Merge Healthcare is recalling Merge Cardio software versions 10.1 and 10.1.1 because the reporting feature times out after one hour of inactivity, causing data loss.

    Product
    Merge Cardio software. Merge Cardio is a system intended to be used to acquire, store, print, transfer, and archive clinical information from Camtronics and other vendors systems including images, hemodynamic studies and reports, measurements (via import from DICOM…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0743-2017·2016-12-21

    Siemens SOMATOM Definition Flash CT Systems Recalled for Software Update

    Siemens is recalling 104 SOMATOM Definition Flash CT systems to install a software and firmware update that fixes bugs and improves performance.

    Product
    SOMATOM Definition Flash System, x-ray, tomography, computed Intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes taken at different angles
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0735-2017·2016-12-21

    C.R. Bard Recalls 70cc Irrigation Syringes Due to Package Defect

    C.R. Bard is recalling 452,728 units of 70cc irrigation syringes because a package defect may compromise product sterility.

    Product
    BARD¿ Irrigation, Syringe 70cc With Resectoscope Tip, Catheter Tip, Luer Adapter And Cap, Rx Only, Sterile, The BARD¿ Syringe is available in a single use plastic design which features a 60cc or 70cc capacity graduated barrel. It has a thumb ring plunger for one-handed use. A…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0763-2017·2016-12-21

    Oculus Recalls Ceramax Skin Barrier Cream Professional Samples

    Oculus Innovative Sciences is recalling professional samples of Ceramax Skin Barrier Cream because they are not meeting stability standards.

    Product
    Ceramax Skin Barrier Cream: NET WT 0.1 OZ (3 g professional sample - not for retail sale) Under the supervision of a health care professional, Ceramax is intended to be used as a topical skin care preparation to relieve and to manage the burning and itching associated with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0736-2017·2016-12-21

    C.R. Bard Recalls 70cc Piston Syringes Due to Package Defect

    C.R. Bard is recalling 70cc Piston Syringes because a package slit defect may compromise product sterility.

    Product
    BARD¿ 70cc Piston Syringe with Catheter Tip, Luer Adapter and Cap, Rx Only, The BARD¿ Syringe is available in a single use plastic design which features a 60cc or 70cc capacity graduated barrel. It has a thumb ring plunger for one-handed use. A catheter adapter tip and Luer…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0754-2017·2016-12-21

    Olympus HF Cable WA00014A Recalled for Software Malfunction

    Olympus Corporation of the Americas is recalling 494 HF Cable WA00014A units due to a software malfunction that may cause incorrect error codes to be generated or displayed.

    Product
    HF Cable WA00014A, Endoscopic electrosurgical unit and accessories
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0756-2017·2016-12-21

    Recall of Sterile Specimen Containers Due to Packaging Defect

    Covidien LLC is recalling 5,187,100 sterile specimen containers because a packaging defect compromised the sterility of the outer surface.

    Product
    Covidien Precision Specimen Container- 4 oz (118 mL), Plastic Screw Top Cap, OR Packaged, Sterile Item Code: 17099
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0737-2017·2016-12-21

    C.R. Bard Recalls Piston Syringes Due to Package Defect Risk

    C.R. Bard is recalling specific lots of 60cc Piston Syringes because a package slit defect may compromise product sterility.

    Product
    BARD¿ Piston Syringe, 60cc, Rx Only, Sterile, The BARD¿ Syringe is available in a single use plastic design which features a 60cc or 70cc capacity graduated barrel. It has a thumb ring plunger for one-handed use. A catheter adapter tip and Luer adapter tip are included. BARD¿…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0742-2017·2016-12-21

    Siemens SOMATOM Definition AS CT Systems Recalled for Software Bug Fixes

    Siemens Medical Solutions USA is recalling 104 SOMATOM Definition AS CT systems to install software and firmware updates that fix bugs and improve performance.

    Product
    SOMATOM Definition AS System, x-ray, tomography, computed Intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes taken at different angles.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0744-2017·2016-12-21

    Siemens SOMATOM Definition Edge CT Systems Recalled for Software Bug Fixes

    Siemens Medical Solutions is recalling 104 SOMATOM Definition Edge CT systems to install a software update that fixes bugs and improves performance.

    Product
    SOMATOM Definition Edge System, x-ray, tomography, computed Intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data from either the same axial plane taken at different angles or spiral planes taken at different angles
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0738-2017·2016-12-21

    C.R. Bard Recalls BARDIA 60cc Piston Irrigation Syringes Due to Package Defect

    C.R. Bard is recalling BARDIA 60cc Piston Irrigation Syringes because a slit defect in the packaging may compromise product sterility.

    Product
    BARDIA¿ 60cc Piston Irrigation Syringe, Sterile, Rx Only, The BARD¿ Syringe is available in a single use plastic design which features a 60cc or 70cc capacity graduated barrel. It has a thumb ring plunger for one-handed use. A catheter adapter tip and Luer adapter tip are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0740-2017·2016-12-21

    BD Recalls Spinal Anesthesia Trays Due to Incorrect Labeling

    Becton Dickinson is recalling 4,500 BD Spinal Anesthesia Trays because a small number were incorrectly labeled as Epidural Trays.

    Product
    BD Spinal Anesthesia Tray The BD Spinal Anesthesia Tray is intended for use by professional anesthesiologists to perform the spinal anesthesia procedure
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0769-2017·2016-12-21

    Natus neoBLUE Phototherapy Systems Recalled for Fiberoptic Pad Failure

    Natus Medical is recalling neoBLUE blanket LED Phototherapy Systems due to early failure of fiberoptic pads, which can cause discoloration and melting at the connector.

    Product
    Updated Natus neoBLUE blanket LED Phototherapy Systems. It provides phototherapy underneath the infant and can be used in a bassinet, open bed, radiant warmer, incubator, or while holding the infant. Affected systems including: 1) Updated light boxes (serial number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0757-2017·2016-12-21

    Pentax Ultrasound Video Bronchoscope Recalled for Incorrect Instructions

    Pentax of America Inc. is recalling 113 Ultrasound Video Bronchoscopes because they shipped with outdated instructions for use.

    Product
    Ultrasound Video Bronchoscope The EB-1970UK, Ultrasound Video Bronchoscope, is intended to provide optical visualization of, ultrasonic visualization of, and therapeutic access to, the Pulmonary Track including but not restricted to organs, tissues, and subsystem: Nasal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0750-2017·2016-12-21

    Roche Recalls LightMix Zika rRT-PCR Test Due to False Positive Risk

    Roche Molecular Systems is recalling the LightMix Zika rRT-PCR Test because the software algorithm may occasionally report false positive results.

    Product
    LightMix¿ Zika rRT-PCR Test The LightMix¿ Zika rRT-PCR Test is a real-time RT-PCR test intended for the qualitative detection of RNA from the Zika virus in serum or EDTA plasma from individuals meeting CDC Zika virus clinical criteria (e.g., clinical signs and symptoms…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0205-2017·2016-12-21

    Jubilant Cadista Recalls Methylprednisolone Tablets Due to Incorrect Expiration Date Labeling

    Jubilant Cadista Pharmaceuticals is recalling 1,512 bottles of Methylprednisolone Tablets, USP, 16 mg, because the expiration date is printed incorrectly as 02/0218 instead of 02/2018.

    Product
    Methylprednisolone Tablets, USP, 16 mg, 50-count bottles, Rx only, Manufactured by Jubilant Cadista Pharmaceuticals Inc., Salisbury, MD 21801, NDC 59746-003-14.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V913000·2016-12-20

    Volkswagen Recalls 2009-2010 Models for ABS Control Unit Failure

    Volkswagen is recalling 2009-2010 Jetta, GTI, Golf, and Audi A3 vehicles because the ABS control unit may fail, potentially causing loss of vehicle control.

    Product
    VOLKSWAGEN — VOLKSWAGEN, AUDI JETTA SPORTWAGEN, JETTA, GTI, GOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·17056·2016-12-20

    Zebra Thermal Printer Power Supply Units Recalled for Fire Hazard

    Zebra Technologies is recalling approximately 166,000 power supply units for thermal printers due to a fire hazard caused by overheating and corrosion.

    Product
    Power supply units for Zebra brand thermal printers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V912000·2016-12-20

    C&M Recalls 2016 Trailers with Missing Front Reflex Reflectors

    C&M Trailers is recalling 670 model year 2016 boat, jet ski, and utility trailers because they may be missing front reflex reflectors, which could make them harder to see.

    Product
    C&M — C&M BOAT TRAILER, JET SKI TRAILER, UTILITY TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V914000·2016-12-20

    BMW, MINI, and Rolls-Royce Recall for Air Bag Initiator Defect

    BMW is recalling 2016-2017 vehicles because seat-mounted air bag initiators may fail to ignite, preventing deployment and increasing injury risk.

    Product
    BMW — BMW, MINI, ROLLS-ROYCE X1 SAV, 550I, M5, 535D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16C008000·2016-12-19

    Baby Trend Recalls Booster Seats Due to Harness Rivet Failure Risk

    Baby Trend is recalling specific Hybrid LX booster seats because a center adjuster rivet may break if used with children over 40 lbs, increasing injury risk in a crash.

    Product
    CHILD SEAT:HARNESS:STRAP/WEBBING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V911000·2016-12-19

    Nissan Recalls Altima, Rogue, and Maxima for Air Bag Sensor Defect

    Nissan is recalling specific 2013-2016 Altima, Rogue, and Maxima vehicles because an incorrect air bag sensor may misclassify front passengers, increasing injury risk in crashes.

    Product
    NISSAN — NISSAN ALTIMA, ROGUE, MAXIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide