The Recall Desk

State

Northern Mariana Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

59126–59150 of 73856

  • ModerateFDA (Devices)·Z-1076-2014·2014-03-05

    Siemens Dimension Vista Enzyme 1 Calibrator Recalled for QC Shifts

    Siemens Healthcare Diagnostics is recalling specific lots of Dimension Vista Enzyme 1 Calibrator due to quality control shifts and imprecision during Pseudocholinesterase calibration.

    Product
    Dimension Vista Enzyme 1 Calibrator (ENZ 1 CAL) lots 3FD034 and 3HD012. An in vitro diagnostic multi-analyte calibrator for the calibration of Amylase (AMY), Gamma-Glutamyl Transferase (GGT), Lactate Dehydrogenase (LDH), Lipase (LIPL), and Pseudocholinesterase (PCHE) methods…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1088-2014·2014-03-05

    Ortho VITROS Chemistry Calibrator Kit 2 Recalled for False Positive Results

    Ortho Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 2 because it may produce false positive serum and plasma sample results.

    Product
    VITROS Chemistry Products Calibrator Kit 2, manufactured by Ortho Clinical Diagnostics 1000 Lee Road Rochester, NY 14606 VITROS Chemistry Products Calibrator Kit 2 is used to calibrate VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems and the VITROS 5600 Integrated System…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1068-2014·2014-03-05

    Smith & Nephew Recalls Renasys EZ PLUS Canisters for Labeling Changes

    Smith & Nephew is recalling Renasys EZ PLUS canisters to modify the bacterial overflow guard and update product labeling.

    Product
    Renasys EZ PLUS, a Canister Component of of Renasys EZ Negative Pressure Wound Therapy System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1067-2014·2014-03-05

    Smith & Nephew Recalls Renasys EZ Canisters for Labeling and Filter Changes

    Smith & Nephew is recalling Renasys EZ canisters to modify the bacterial overflow guard and update product labeling.

    Product
    Renasys EZ, a Canister Component of of Renasys EZ Negative Pressure Wound Therapy System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1565-2014·2014-03-05

    Mars Recalls Uncle Ben's Garlic & Butter Rice Due to Flushing Reports

    Mars Food US is recalling Uncle Ben's Infused Rice Garlic & Butter Flavor after reports of mild flushing reactions that resolved within two hours.

    Product
    Uncle Ben's (R), Infused(R) Rice Garlic & Butter Flavor, net weight 5 LB (2.27kg), Distributed by MARS foodservices US, P.O. Box 5059, Rancho Dominguez, CA 90224-5059
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1566-2014·2014-03-05

    Mars Recalls Uncle Ben's Rice Pilaf Due to Mild Flushing Reports

    Mars Food US is recalling Uncle Ben's Infused Rice Pilaf after reports of mild flushing reactions that resolved within two hours.

    Product
    Uncle Ben's (R), Infused(R) Rice Pilaf, net weight 5 LB (2.27kg), Distributed by MARS foodservices US, P.O. Box 11547, Carson, CA 90749-11547
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1095-2014·2014-03-05

    Cardiovascular Systems Recalls Diamondback 360 Coronary Orbital Atherectomy Devices

    Cardiovascular Systems, Inc. is recalling 318 Diamondback 360 Coronary Orbital Atherectomy Devices because they mistakenly contain a saline line not approved for coronary use.

    Product
    CSI, Diamondback 360 Coronary Orbital Atherectomy System, Part Number 70058-02, Model Number DBEC-125 Product Usage: The system is indicated to facilitate stent delivery in patients with coronary artery disease (CAD) who are acceptable candidates for PTCA or stenting due to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1107-2014·2014-03-05

    Philips HeartStart XL+ Defibrillator Recalled for Battery Charge Time Labeling Error

    Philips is recalling 7,157 HeartStart XL+ Defibrillators because the battery charge time at high temperatures is slightly longer than the 3 hours stated in the labeling.

    Product
    Philips HeartStart XL+ Defibrillator/Monitor Model: 861290 The HeartStart XL+ is intended for use in a hospital setting by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced life support or…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1568-2014·2014-03-05

    Mars Recalls Uncle Ben's Spanish Flavor Rice Due to Flushing Reports

    Mars Food US is recalling Uncle Ben's Spanish Flavor Rice after reports of mild flushing reactions that resolved within two hours.

    Product
    Uncle Ben's (R), Infused(R) Rice Spanish Flavor, net weight 25 LB (11.34 kg), Distributed by MARS foodservices US, P.O. Box 5059, Rancho Dominguez, CA 90224-5059
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1086-2014·2014-03-05

    Ranbaxy Recalls Atorvastatin Calcium Tablets Due to Foreign Tablet Presence

    Ranbaxy Inc. is recalling 64,626 bottles of Atorvastatin Calcium 10 mg tablets because a 20 mg tablet was found inside a sealed 10 mg bottle.

    Product
    ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1111-2014·2014-03-05

    Roche Recalls Leaking cobas PCR Urine and Swab Test Kits

    Roche Molecular Systems is recalling 84 batches of cobas PCR Urine, Female Swab, and media kits due to reports of leaking media.

    Product
    cobas¿ PCR Urine Kit 100 PKT IVD cobas¿ PCR Female Swab Kit 100 PKT IVD cobas¿ PCR media 100T IVD cobas¿ PCR Female Swab Kit 100 PKT JPN-IVD Roche Molecular Systems, Inc. Branchburg, NJ 08876 USA Roche Diagnostics 9115 Hague Road Indianapolis, IN 46250-0457 The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1093-2014·2014-03-05

    Dako HER2 CISH pharmDx Kit Recalled Due to Weak Red Signals

    Dako North America Inc. is recalling 49 units of the HER2 CISH pharmDx Kit because weak red signals have been observed.

    Product
    Product Name: HER2 CISH pharmDx Kit Catalog/Model number: SK109, lot 20000910 Product Usage: For in vitro diagnostic use. HER2 CISH pharmDx Kit is intended for dual-color chromogenic visualization of signals achieved with directly labeled in situ hybridization probes…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1591-2014·2014-03-05

    Novartis Recalls Benefiber Fiber Supplement Stick Packs Due to Consumer Complaints

    Novartis Consumer Health is recalling specific lots of Benefiber fiber supplement stick packs nationwide due to a high number of consumer complaints.

    Product
    Benefiber fiber supplement stick packs, sugar free and taste free, packaged in the following configurations: (1) Benefiber Fiber Supplement, On-The-Go Stick Packs, Sugar Free, Clear & Taste-Free, packaged in 8.16-oz. boxes containing 68/0.12-oz. stick packs, UPC 300670176686.…
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1121-2014·2014-03-05

    Medtronic Everest 20cc Inflation Device Recalled for Incorrect Master Label

    Medtronic Vascular is recalling 191 Everest 20cc Inflation Devices due to an incorrect master label. The devices are sterile, single-use tools used to inflate balloon catheters.

    Product
    Medtronic Everest 20cc Inflation Device; Model Number and Catalog Number: AC2205P The Everest 20cc Inflation device is designed to be used to inflate / deflate balloon catheters as well as to monitor pressure within the balloon. The Everest 20atm Device is outfitted with a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1090-2014·2014-03-05

    Gilead Recalls Atripla Tablets Due to Foreign Silicone Particulates

    Gilead Sciences is recalling specific lots of Atripla tablets because they contain red silicone rubber particulates. The recall covers 39,223 bottles distributed nationwide.

    Product
    Atripla (efavirenz 600 mg/ emtricitabine 200 mg/ tenofovir disoproxil fumarate 300 mg) Tablets, 30 Tablet Bottles, Rx only. Manufactured for: Bristol-Myers Squibb & Gilead Sciences, LLC, Foster City, CA 94404. Made in Ireland. NDC 15584-0101-1. Manufactured for…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V087000·2014-03-04

    New Flyer Transit Buses Recalled for Potential Exhaust Fire Risk

    New Flyer is recalling certain transit buses because condensation in the intake manifold may freeze, causing sensor issues that could lead to exhaust flames or vehicle fires.

    Product
    NEW FLYER — NEW FLYER C40LF, C40LFR, C35LF, C35LFR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V095000·2014-03-04

    Prevost Recalls 2013-2014 Coaches Due to Battery Cable Insulation Defect

    Prevost is recalling 59 model year 2013-2014 coaches because defective battery cable insulation may cause the engine to shut down, increasing crash risk.

    Product
    PREVOST — PREVOST H3-45 VIP, H3-45, H3-41
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V097000·2014-03-04

    Ford E-Series CNG Conversion Recall for Rear Cylinder Bracket Failure

    Landi Renzo USA is recalling 2011-2014 Ford E-150, E-250, and E-350 vans modified for CNG because rear cylinder brackets may fail, risking a gas leak and fire.

    Product
    FORD — FORD E-150, E-350, E-250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V103000·2014-03-04

    Fiat 500L Recall: Transmission Shifter May Fail to Shift Gears

    Chrysler is recalling 2014 Fiat 500L vehicles because the transmission shifter may not respond to driver input, potentially causing unintended vehicle movement.

    Product
    FIAT — FIAT 500L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V098000·2014-03-04

    Newmar Recalls 2013-2014 RVs Due to Microwave Fire Risk

    Newmar is recalling 599 recreational vehicles from 2013-2014 because the built-in microwave may start on its own, posing a fire hazard if contents are inside.

    Product
    NEWMAR — NEWMAR VENTANA LE, ESSEX, BAY STAR, BAY STAR SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V091000·2014-03-04

    Volvo Bus 9700 Recall: Sliding Seat Locking Defect

    Volvo is recalling 2009-2014 9700 coaches with wheelchair lifts because sliding seats may not latch correctly, increasing injury risk in a crash.

    Product
    VOLVO BUS — VOLVO BUS 9700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V096000·2014-03-04

    Prevost Recalls 2011-2012 Coaches Due to Fire Suppression Tank Issue

    Prevost is recalling 2011-2012 X3 and XLII coaches because the fire suppression tank may discharge prematurely, leaving the system unavailable during a fire.

    Product
    PREVOST — PREVOST X3, XLII
    Category
    Vehicle
    Distribution
    Distributed nationwide