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.

55401–55425 of 73850

  • HighFDA (Devices)·Z-1014-2015·2015-02-04

    Clinical Innovations Recalls Ebb Complete Tamponade System Due to Balloon Leak Risk

    Clinical Innovations, LLC is recalling 827 units of the Ebb Complete Tamponade System because of a potential for balloon leaks in lots manufactured since August 2014.

    Product
    Ebb Complete Tamponade System, BD-OTS Obstetric Catheter, REF CTS-1000, Rx Only, Sterile EO
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1020-2015·2015-02-04

    Sunrise Medical Recalls Six Quickie Q7 Adult Rigid Wheelchairs

    Sunrise Medical is recalling six Quickie Q7 Adult Rigid Wheelchairs because the height-adjustable handle may dislodge due to failing locking mechanisms.

    Product
    Quickie Q7 Adult Rigid Wheelchair Model EIR4.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1023-2015·2015-02-04

    Beckman Coulter Lipase Assay Recalled Due to NAC Interference

    Beckman Coulter is recalling Lipase Assay kits because N-acetyl cysteine can cause falsely low results.

    Product
    Beckman Coulter, Lipase Assay, Catalog No. OSR6X30
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1012-2015·2015-02-04

    Aesculap Miethke Shunt System Accessories Recalled for Incorrect MR Safety Labeling

    Aesculap, Inc. is recalling Miethke Shunt System accessories because the shelf box labels incorrectly display an MR conditional symbol. The product is actually MR unsafe, and the correct information is only provided in the Instructions for Use.

    Product
    Miethke Shunt System accessories Product Usage: - The Miethke Shunt System is intended to shut cerebrospinal fluid from the lateral ventricles of the brain into the peritoneum.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1024-2015·2015-02-04

    Beckman Coulter Uric Acid Assay Recalled Due to NAC Interference

    Beckman Coulter is recalling Uric Acid Assay kits because N-acetyl cysteine administration can cause falsely low test results.

    Product
    Beckman Coulter, Uric Acid Assay, Catalog No. OSR6X98
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0380-2015·2015-02-04

    Baxter Recalls Fluconazole Injection Bags Due to Seal Defects

    Baxter Healthcare is recalling 31,130 bags of Fluconazole Injection due to potential leaks from incomplete seals, which may compromise sterility.

    Product
    FLUCONAZOLE — FLUCONAZOLE (FLUCONAZOLE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1026-2015·2015-02-04

    Beckman Coulter Lactate Assay Recalled Due to NAC Interference

    Beckman Coulter is recalling Lactate Assay kits because N-acetyl cysteine (NAC) administration can cause falsely low test results.

    Product
    Beckman Coulter, Lactate Assay, Catalog No. OSR6X93
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1025-2015·2015-02-04

    Beckman Coulter Cholesterol Assay Recalled Due to NAC Interference

    Beckman Coulter is recalling Cholesterol Assay kits because N-acetyl cysteine administration can cause falsely low results.

    Product
    Beckman Coulter, Cholesterol Assay, Catalog No. OSR6X16
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1027-2015·2015-02-04

    Siemens Syngo.plaza PACS Recalled for Potential Image Loss During System Crashes

    Siemens Medical Solutions is recalling 50 Syngo.plaza PACS systems because images may be lost if the system crashes before saving data to the hard disk.

    Product
    Syngo.plaza: Syngo.plaza is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images. It supports the physician in diagnosis and treatment planning. Syngo.plaza also…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1032-2015·2015-02-04

    Fresenius Kabi Recalls HEPFLUSH-10 Heparin Lock Flush Solution Due to pH Failure

    Fresenius Kabi is recalling HEPFLUSH-10 heparin lock flush solution because a specific lot failed pH specifications. The recall covers 69,725 units distributed nationwide.

    Product
    HEPFLUSH-10 (HEPARIN LOCK FLUSH SOLUTION, USP) 100 USP units per 10 mL (10 USP units per mL), Single Dose Vial, Rx only -- Fresenius Kabi USA, LLC -- NDC 63323-017-10, Product Code 1710
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·028-2015·2015-02-04

    Krehbiels Specialty Meats Recalls Pork Bratwurst Due to Misbranding

    Krehbiels Specialty Meats is recalling approximately 29 pounds of pork bratwurst because the label failed to list all ingredients due to a printing error.

    Product
    Krehbiels Specialty Meats Inc — Recall Notification Report 028-2015 (Bratwurst)
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1030-2015·2015-02-04

    Arrow Medical Kits Recalled for Incorrect Biopatch Dressing Size

    Arrow International Inc. is recalling specific medical kits because they were packaged with the incorrect size Biopatch Dressing. No risk to patients is anticipated.

    Product
    Arrow Select Kits (ASK), Maximal Barrier Precautions Kits (CDC) and Arterial Catheterization Kit (NA) with Biopatch Dressing
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V057000·2015-02-03

    Mack Pinnacle Trucks Recalled for Brake Reservoir Defect

    Mack is recalling 2014-2015 Pinnacle trucks because a smaller air reservoir may increase stopping distance, raising crash risk.

    Product
    MACK — MACK PINNACLE (CXU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V061000·2015-02-03

    Newmar Recalls 2014-2015 King Aire and Essex Vans for Brake Valve Defect

    Newmar is recalling 98 model year 2014-2015 King Aire and Essex vehicles because a damaged valve diaphragm may reduce air pressure, potentially compromising braking performance.

    Product
    NEWMAR — NEWMAR KING AIRE, ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V060000·2015-02-03

    Blue Bird Recalls 2011-2016 All American Buses for Exhaust Hanger Failure

    Blue Bird is recalling 2011-2016 All American rear engine transit buses because exhaust system hangers may fail, potentially causing housings to fall onto the roadway.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V055000·2015-02-02

    Husqvarna FE 350 S and FE 501 S Recalled for Front Fork Defect

    KTM is recalling 2015 Husqvarna FE 350 S and FE 501 S motorcycles because the front fork piston rod may not be tightened correctly, increasing crash risk.

    Product
    HUSQVARNA — HUSQVARNA FE 501 S, FE 350 S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V054000·2015-02-02

    Nissan Recalls Infiniti and GT-R Vehicles for Steering Column Defect

    Nissan is recalling specific 2008-2009 Infiniti and Nissan GT-R vehicles because a steering column defect may cause loss of steering, increasing crash risk.

    Product
    INFINITI — INFINITI, NISSAN EX35, GT-R, FX35, FX45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V056000·2015-02-02

    Mack Recalls 2015 LEU Trucks Due to Door Latch Defect

    Mack is recalling 2015 LEU trucks because a short door component may prevent opening from inside, hindering emergency egress.

    Product
    MACK — MACK LEU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V053000·2015-02-02

    Brammo Recalls 2013-2014 Empulse Motorcycles Due to Oil Leak Hazard

    Brammo is recalling 2013-2014 Empulse and Empulse R motorcycles because oil may leak from the transmission onto the rear tire, increasing crash risk.

    Product
    BRAMMO — BRAMMO EMPULSE, EMPULSE R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V051000·2015-01-30

    PACCAR Recalls 2015 Peterbilt and Kenworth Trucks for Brake Caliper Bolt Issue

    PACCAR is recalling 106 model year 2015 Peterbilt and Kenworth trucks because brake caliper bolts may not be properly torqued, which could reduce braking effectiveness.

    Product
    PETERBILT — PETERBILT, KENWORTH 210, K370, 320, K270
    Category
    Vehicle
    Distribution
    Distributed nationwide