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.

56126–56150 of 73850

  • ModerateFDA (Drugs)·D-0249-2015·2014-11-26

    Prometheus Recalls Mercaptopurine Tablets for Failed Dissolution Specifications

    Prometheus Laboratories is recalling Mercaptopurine Tablets 50mg because the product failed dissolution specifications during stability testing.

    Product
    Mercaptopurine Tablets, USP 50mg, a) 60-count bottle (NDC 49884-922-02), b) 250-count bottle (NDC 49884-922-04), RX only, Manufactured by Stason Pharmaceuticals, Inc., 11 Morgan, Irvine, CA 92618 for Prometheus Laboratories, Inc., 9410 Carroll Park Drive, San Diego, CA 92121
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0214-2015·2014-11-26

    Siemens ADVIA Centaur Cleaning Solution Recalled for Stability Concerns

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur Cleaning Solution because its stability is not assured. The product is used in in vitro diagnostic systems.

    Product
    ADVIA Centaur¿ and ADVIA Centaur¿ XP and ADVIA Centaur¿ CP Cleaning Solution (For in vitro diagnostic use with the ADVIA¿ Centaur systems) Catalog Number: 112748 (Siemens Material Number (SMN): 10310041 The Cleaning Solution is a component of the ADVIA Centaur¿ and ADVIA…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1589-2014·2014-11-26

    Medtronic Recalls AxIEM CR Tumor Resection Devices Due to Sterility Concerns

    Medtronic Navigation is recalling 26,674 AxIEM CR tumor resection devices because returned units may not have been properly inspected for damage that could compromise sterility.

    Product
    PACK 9731975 TUMOR RESECTION AXIEM CR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1592-2014·2014-11-26

    Medtronic Recalls Sterile Percutaneous Pins Due to Sterility Control Issues

    Medtronic Navigation is recalling 26,674 sterile percutaneous pins because returned devices may not have been properly examined for damage to ensure sterility.

    Product
    PIN, 9733235, 100MM, STERILE, PERC REF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1598-2014·2014-11-26

    Medtronic Recalls Traj Guide Kits Due to Sterility Control Issues

    Medtronic Navigation is recalling 26,674 Traj Guide Kits because returned devices may not have been properly inspected for damage that could compromise sterility.

    Product
    TRAJ GUIDE KIT, 9733066, BIOPSY, INT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1587-2014·2014-11-26

    Medtronic Recalls Thoracic Tactile Probes Due to Sterility Control Issues

    Medtronic Navigation is recalling 26,674 thoracic tactile probe kits because returned devices may not have been properly examined for damage to ensure sterility.

    Product
    KIT, 9731427, THORACIC TACTILE PROBES
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1584-2014·2014-11-26

    Medtronic Recalls ENT Navigation Devices Due to Sterility Control Issues

    Medtronic Navigation is recalling 26,674 ENT PRGM 9734636 ADD FUSION NAV AxiEM devices because returned units may not have been properly examined for damage to ensure sterility.

    Product
    ENT PRGM 9734636 ADD FUSION NAV AxiEM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1601-2014·2014-11-26

    Medtronic Recalls Tumor Resection Kits Due to Sterility Control Issues

    Medtronic Navigation is recalling 26,674 Tumor Resection Kits because returned devices may not have been properly examined for damage to ensure sterility.

    Product
    TUMOR RESECTION KIT 9733608 SKULL MOUNT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1597-2014·2014-11-26

    Medtronic Recalls Traj Guide Kits Due to Sterility Control Issues

    Medtronic Navigation is recalling 26,674 Traj Guide Kits because returned devices may not have been properly inspected for damage that could compromise sterility.

    Product
    TRAJ GUIDE KIT, 9733065, BIOPSY, EXT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0229-2015·2014-11-26

    Siemens Recalls ADVIA Centaur BNP Assay Reagents Due to Labeling Error

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur BNP Assay reagents because approximately 2,000 ReadyPacks contain an incorrect human-readable side label.

    Product
    ADVIA Centaur BNP Assay for in vitro diagnostic use in the quantitative determination of B-type Natriuretic Peptide (BNP) in human plasma using the ADVIA Centaur, Centaur XP, Centaur CP Systems; Catalog Numbers: Cat No. 02816138/SMN 10309044 (100 test) 02816634/SMN 10309045…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0230-2015·2014-11-26

    Biomerieux Recalls Etest Ceftaroline Devices Due to Incorrect Expiration Date Labeling

    Biomerieux is recalling 652 Etest Ceftaroline devices because the labels list a 5-year expiration date instead of the correct 2-year date.

    Product
    Etest¿ Ceftaroline (CPT32) WW B30. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for determining the antimicrobial susceptibility of Gram negative and Gram positive aerobic bacteria.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0231-2015·2014-11-26

    Biomerieux Recalls Etest Ceftaroline Devices Due to Incorrect Expiration Date

    Biomerieux is recalling 652 Etest Ceftaroline devices because the labels list a 5-year expiration instead of 2 years.

    Product
    Etest¿ Ceftaroline (CPT32) WWB100. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for determining the antimicrobial susceptibility of Gram negative and Gram positive aerobic bacteria.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0233-2015·2014-11-26

    Biomerieux Recalls Etest Ceftaroline Devices Due to Incorrect Expiration Date

    Biomerieux is recalling 652 Etest Ceftaroline devices because the labels list a 5-year expiration date instead of the correct 2-year date.

    Product
    Etest¿ Ceftaroline (CPT32) US B100. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for determining the antimicrobial susceptibility of Gram negative and Gram positive aerobic bacteria.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0254-2015·2014-11-26

    Hospira Recalls Vancomycin Hydrochloride Vials Due to Mislabeling

    Hospira Inc. is recalling 316,640 vials of Vancomycin Hydrochloride for Injection because product trays were mislabeled to contain a different product.

    Product
    VANCOMYCIN HYDROCHLORIDE — VANCOMYCIN HYDROCHLORIDE (VANCOMYCIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0232-2015·2014-11-26

    Biomerieux Recalls Etest Ceftaroline Devices Due to Incorrect Expiration Date Labeling

    Biomerieux is recalling 652 Etest Ceftaroline devices because the labeling displays a 5-year expiration period instead of the correct 2-year period.

    Product
    Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for determining the antimicrobial susceptibility of Gram negative and Gram positive aerobic bacteria.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0234-2015·2014-11-26

    Biomerieux Recalls Etest Ceftaroline Devices Due to Incorrect Expiration Date

    Biomerieux is recalling 652 Etest Ceftaroline devices because the labeling displays a 5-year expiration instead of the correct 2-year period.

    Product
    Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for determining the antimicrobial susceptibility of Gram negative and Gram positive aerobic bacteria.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·15036·2014-11-25

    Goal Zero Sherpa 50 and 120 Battery Packs Recalled for Fire Hazard

    Goal Zero is recalling Sherpa 50 and 120 rechargeable battery packs because they can overheat and catch fire. Consumers should stop using the units and contact the company for a free replacement.

    Product
    Goal Zero Sherpa brand 50 and 120 rechargeable battery packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V753000·2014-11-25

    Aston Martin Recalls 2006-2014 Models for Seat Heater Overheating Risk

    Aston Martin is recalling 7,256 vehicles because a faulty seat heater module may prevent the heaters from turning off, creating a risk of overheating and injury.

    Product
    ASTON MARTIN — ASTON MARTIN V8 VANTAGE, DBS, DB9, V12 VANTAGE COUPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15037·2014-11-25

    Pro Armor Recalls Utility Vehicle Doors Due to Latch Failure

    Pro Armor is recalling about 300 utility vehicle doors for Polaris RZR models because the latch pin can disengage, posing impact and laceration hazards.

    Product
    Utility vehicle doors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V751000·2014-11-24

    Capacity Recalls 2014 ISB13 Trucks Due to Fuel Filter Defect

    Capacity is recalling 2014 ISB13 trucks because a fuel filter defect may cause the engine to stall without warning, increasing the risk of a crash.

    Product
    CAPACITY — CAPACITY ISB13
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V750000·2014-11-24

    Harley-Davidson Recalls 2015 Tri-Glide Motorcycles Due to Rear Brake Defect

    Harley-Davidson is recalling 1,560 model year 2015 Tri-Glide motorcycles because a defective rear brake master cylinder piston may cause brake failure and increase crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHTCUTG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V747000·2014-11-24

    Spartan Trucks Recalled for Air Brake Valve Defect

    Spartan is recalling 2013-2015 trucks because damaged air brake valves may reduce braking performance or cause parking brakes to reapply, increasing crash risk.

    Product
    SPARTAN — SPARTAN GLADIATOR, DR, NVS, MM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V748000·2014-11-24

    Champion Transit Bus Recall for Defective Passenger Seat Spring Nuts

    Champion is recalling 2014-2015 transit buses because defective spring nuts may fail to secure passenger seats, increasing injury risk in a crash.

    Product
    CHAMPION — CHAMPION CHALLENGER, CRUSADER, DEFENDER, HCAC
    Category
    Vehicle
    Distribution
    Distributed nationwide