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.

56526–56550 of 73850

  • ModerateFDA (Devices)·Z-0093-2015·2014-10-29

    McKesson Cardiology Hemo Software Recall Due to Insufficient Maintenance Communication

    McKesson Information Solutions LLC is recalling 625 McKesson Cardiology Hemo devices because communication regarding required annual maintenance testing was insufficient.

    Product
    McKesson Cardiology Hemo. McKesson Cardiology" Hemo is intended for complete physiological/hemodynamic monitoring, clinical data acquisition, medical image and data processing, and analytical assessment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0028-2015·2014-10-29

    Bio-Pharm Recalls Acetaminophen Oral Suspension Due to Assay Failure

    Bio-Pharm, Inc. is recalling one lot of Acetaminophen Oral Suspension Liquid 160mg/5mL because the product failed the assay at the 6-month timepoint.

    Product
    Rugby Children's Pain and Fever Acetaminophen Oral Suspension 160 mg/5 mL, Cherry Flavor, 2 FL. oz bottle, OTC, Distributed by: Rugby Laboratories Livonia, MI 48150, NDC 0536-3606-96 Major Children's Mapap Suspension Liquid, Cherry Flavor, 4 FL OZ bottle, OTC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0107-2015·2014-10-29

    Mindray V-Series Patient Monitor Recalled for Drug Calculator Function Issue

    Mindray DS USA is voluntarily recalling V-Series Patient Monitors due to a software issue with the Drug Calculator function.

    Product
    Mindray V21, Size: 515 mm X 335 mm X 685 mm, N.W.: 8 kg, G.W.: 11 kg, Qty:1 The V-Series Monitor is intended for intra hospital use under the direct supervision of a licensed healthcare practitioner. The indications for use include the monitoring of ECG waveform derived from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0036-2015·2014-10-29

    Forest Pharmaceuticals Recalls Bystolic Tablets for Dissolution Failure

    Forest Pharmaceuticals is recalling Bystolic (nebivolol) 20 mg tablets because they failed a dissolution specification at a 6-month stability time point.

    Product
    Bystolic (nebivolol) tablets, 20 mg/tablet, packaged as 7 tablets/bottle/carton, and 12 bottles/trays, Professional Sample, Rx only, Forest Pharmaceuticals, Inc., St. Louis, MO. --- NDC 0456-1420-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0108-2015·2014-10-29

    St. Jude Medical Recalls Fast-Cath Trio Hemostasis Introducer Due to Dilator Defect

    St. Jude Medical is voluntarily recalling 220 units of the Fast-Cath Trio Hemostasis Introducer because the dilator is too small to allow guidewire advancement, potentially causing procedural delays.

    Product
    St Jude Medical, 10F Fast-Cath Trio" Hemostasis Introducer, REF # 406308, Sterile EO. The Fast-Cath Trio" Hemostasis Introducer consists of the following components: Port hemostasis adapter (3), Sheath (10F Cath-Lock"), dilator (10F) and 0.038 guidewire. See product…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0099-2015·2014-10-29

    Intra Pump Infusion Systems Recalls CRN Crono Syringes Due to Needle Debris

    Intra Pump Infusion Systems is recalling CRN Crono Syringes because the needle tips may contain clear debris. The recall affects 25,440 units distributed in the US and Canada.

    Product
    CRN Crono Syringe CRN20 with 19G x 1 "Steel Needle"
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0118-2015·2014-10-29

    Aerogen Recalls FRIWO Power Adapters for Aeroneb Nebulizer Systems

    Aerogen is recalling FRIWO AC/DC power adapters for Aeroneb nebulizers because the cover may break and dislodge before use.

    Product
    The Aeroneb Professional Nebulizer System is a portable medical device for multiple patient use that is intended to aerosolize physician-prescribed solutions for inhalation to patients on and off ventilation or other positive pressure breathing assistance. The Aeroneb…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0041-2015·2014-10-29

    ZEE Aspirin Recalled for Incorrect Inactive Ingredient Labeling

    ZEE Medical is recalling ZEE Aspirin 325mg tablets because the product label incorrectly lists inactive ingredients.

    Product
    ZEE Aspirin 325mg - 24 tablets in single dose packets, OTC, Manufactured for ZEE Medical Inc., Irvine,CA 92606 by ULTRA Tab Laboratories, Inc. Highland, NY 12528
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0122-2015·2014-10-29

    Siemens IMMULITE 1000 Cortisol Assay Recalled for Positive Bias

    Siemens Healthcare Diagnostics is recalling specific lots of IMMULITE 1000 Cortisol Assay reagents due to confirmed positive bias on controls.

    Product
    IMMULITE /IMMULITE 1000 Systems COR Cortisol, REF/Catalog Number LKC01, SMN 10381388, IVD. For in vitro diagnostic use with the IMMULITE 1000 Systems Analyzers for the quantitative measurement measurement of cortisol (hydrocortisone, Compound F) in serum, as an aid in the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0101-2015·2014-10-29

    Estill Medical Recalls Ultra Battery 1 for Insufficient Charging Capacity

    Estill Medical Technologies is recalling 6,886 Ultra Battery 1 units because they may not reach full charge capacity within the standard 60-minute charging period.

    Product
    Ultra Battery 1 Model: TA-UB1 NSN: 6515-01-592-5803 The Ultra Battery 1 (TA-UB1) is a rechargeable power source for the Thermal Angel Blood and IV Fluid Infusion Warmer. The TA-UB1 battery was designed to provide sufficient power for the Thermal Angel to warm and deliver one…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0043-2015·2014-10-29

    American Health Packaging Recalls Subpotent Methylprednisolone Tablets

    American Health Packaging is recalling 2,005 cartons of Methylprednisolone 4 mg tablets because they failed to meet potency standards at a 6-month stability time point.

    Product
    METHYLPREDNISOLONE — METHYLPREDNISOLONE (METHYLPREDNISOLONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·14E070000·2014-10-28

    Meritor Wabco Recalls Quick Release Valves Due to Air Pressure Loss

    Meritor Wabco is recalling specific Quick Release Valves where damaged rubber diaphragms may reduce air pressure, potentially compromising braking performance.

    Product
    SERVICE BRAKES, AIR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V672000·2014-10-27

    Honda Recalls 2014 Grom125 and NSS300 Motorcycles for Fuel Pump Defect

    Honda is recalling 2014 Grom125 and NSS300 motorcycles because a fuel pump bracket may swell and seize, causing the bike to stall and increasing crash risk.

    Product
    HONDA — HONDA GROM125, NSS300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V674000·2014-10-27

    BMW Recalls 2014 i8 Vehicles for Potential Fuel Tank Weld Defect

    BMW is recalling 223 model year 2014 i8 vehicles because a ground cable bolt may not be properly welded to the fuel tank, creating a risk of fuel leaks and fire.

    Product
    BMW — BMW I8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·074-2014·2014-10-25

    Murry's Recalls Gluten-Free Chicken Products Due to Staphylococcal Enterotoxin

    Murry's Inc. is recalling approximately 31,689 pounds of gluten-free breaded chicken products due to potential Staphylococcal enterotoxin contamination.

    Product
    Pennsylvania Firm Recalls Chicken Products Due to Staphylococcal Enterotoxin Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V667000·2014-10-24

    Audi Recalls 2013-2015 Models Due to Air Bag Deployment Software Defect

    Volkswagen Group of America is recalling 2013-2015 Audi A4, S4, and Allroad vehicles because a software error may prevent front air bags from deploying in a secondary impact.

    Product
    AUDI — AUDI S4, ALLROAD, A4 ALLROAD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V668000·2014-10-24

    Nissan Recalls Infiniti QX56 and QX80 for Air Bag Defect

    Nissan is recalling 2013 Infiniti QX56 and 2014 QX80 vehicles because the driver's air bag inflator may contain an incorrect part that could rupture during deployment.

    Product
    INFINITI — INFINITI QX80, QX56
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V670000·2014-10-24

    Volkswagen Recalls 2015 Jetta and Passat for Seatback Recliner Defect

    Volkswagen is recalling 2015 Jetta and Passat vehicles because a seatback recliner bracket may not engage correctly, causing unexpected movement that could distract the driver.

    Product
    VOLKSWAGEN — VOLKSWAGEN PASSAT, JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide