The Recall Desk

State

Northern Mariana Islands product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47151–47175 of 73840

  • CriticalFDA (Food)·F-1853-2016·2016-08-10

    ACH Food Companies Recalls Salad Toppings for Listeria Risk

    ACH Food Companies is recalling Durkee, Hy-Vee, and Food Club salad toppings because an ingredient may be contaminated with Listeria monocytogenes.

    Product
    Salad topping labeled under the following brand names: (Product 1) Durkee Salad Topping in plastic bottle, Net Wt. 6.75 oz (192 g), packed in cases of 12. UPC 047600091366. The responsible firm name on the label is ACH Food Companies, Inc. Memphis, TN; (Product 2) Hy-Vee…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V592000·2016-08-10

    Tadano Recalls 2013-2015 All-Terrain Cranes Due to Air Line Defect

    Tadano is recalling 2013-2015 all-terrain crane trucks because an improperly assembled air line connection may cause reduced braking or loss of mobility.

    Product
    TADANO — TADANO ATF70G-4, ATF220G-5, ATF130G-5, ATF400G-6
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2339-2016·2016-08-10

    Zimmer Air Dermatome II Width Plate Recalled for Surface Coating Defects

    Zimmer Surgical Inc is recalling 90 units of Air Dermatome II Width Plates because the surface coating is blistering, peeling, and discoloring after use.

    Product
    Zimmer¿ Air Dermatome II Width Plate, 3 inch. Part #00-8851-203-00. Width plate is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2215-2016·2016-08-10

    Draeger Recalls Oxylog 3000 Pediatric Patient Circuits Due to Leakage

    Draeger Medical is recalling Oxylog 3000 disposable pediatric patient circuits because isolated episodes of leakage were found at the check valve.

    Product
    Oxylog 3000, Disposable Pediatric Patient Circuit, Catalog Number: 5704964 The VentStar Oxylog 3000F disposable pediatric patient breathing circuit is used with the Dr¿ger Oxylog 3000 and Oxylog 3000 plus Emergency Transport Ventilators.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1871-2016·2016-08-10

    Honey Bunchies Gourmet Honey Bars Recalled for Listeria Risk

    Honey Bunchie, LLC is voluntarily recalling Honey Bunchies Gourmet Honey Bars due to potential Listeria monocytogenes contamination in sunflower kernels.

    Product
    Honey Bunchies Gourmet Honey Bars, 1.9 oz. snack bar containing honey, sunflower kernels, peanuts and pecans. Packaging: Box containing 20 individual bars in plastic wrappers. Manufactured by: Honey Bunchie, LLC, Longmont, CO. Individual Bar UPC 8 66192 00010 1; Box of 20 Bars…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2255-2016·2016-08-10

    Olympus Analytical X-Ray Systems Recalled for Trigger Lock Failure

    Olympus Scientific Solutions Americas is recalling Analytical X-Ray Systems because the trigger lock may fail to prevent x-ray generation in test modes.

    Product
    Olympus Scientific Solutions Americas Corporation (OSSA) Model: Analytical X-Ray System X -Ray Fluorescence. Intended to emit ionizing radiation Delta with models: DC-2000, DC-4000, DC-6000, DI-2000, DP-2000, DP-4000, DP-4050, DP- 6000, DPO-4000, DPO-6000, DS-2000…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V590000·2016-08-10

    Jeep Cherokee Recall for Loose Seat Fasteners

    Chrysler is recalling 2014-2016 Jeep Cherokee vehicles because seat fasteners may not be tightened correctly, increasing injury risk in a crash.

    Product
    JEEP — JEEP CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1452-2016·2016-08-10

    Let's Talk Health Recalls Unapproved Oxygen Nasal Wash Solution

    Let's Talk Health is recalling 417 bottles of Oxygen Nasal Wash because the product was marketed without FDA approval and does not comply with nasal decongestant monograph requirements.

    Product
    Oxygen Nasal Wash (purified water, xylitol, stabilized oxygen, sodium chloride) solution, .75 oz (22mL) bottle, Distributed by: Let's Talk Health, Chula Vista, CA 91914.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·16242·2016-08-10

    Dennis East International Recalls Whiskey Glass and Stone Sets

    Dennis East International is recalling whiskey glass and stone sets because the glass can break during use, posing a laceration risk.

    Product
    Whiskey Glass and Stone Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2341-2016·2016-08-10

    Merge HEMO software recall for inaccurate INR display

    Merge Healthcare is recalling 37 units of Merge HEMO software because the displayed International Normalized Ratio (INR) value does not match the imported value.

    Product
    Merge HEMO software.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2305-2016·2016-08-10

    Philips MultiDiagnost Eleva X-Ray System Recalled for Potential Bolt Failure

    Philips is recalling 993 MultiDiagnost Eleva x-ray systems because bolts attaching the clamping plate may break, causing the C-arm to sag.

    Product
    MultiDiagnost Eleva with Flat Detector; x-ray system. Product Codes: 708034, 708037, 708038.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16243·2016-08-10

    Shocker RSX Paintball Markers Recalled for Chamber Ejection Risk

    Shocker Paintball is recalling RSX markers with blue main chambers because the part can unexpectedly eject from the rear, posing a risk of impact injury.

    Product
    Shocker RSX paintball markers/guns
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2331-2016·2016-08-10

    Stryker Recalls Spirit Plus Hospital Beds Due to Actuator Failure

    Stryker Medical is voluntarily recalling Spirit Plus hospital beds because broken actuators may cause the bed to lower unexpectedly, risking patient injury.

    Product
    Spirit Plus Bed, A-C Powered Hospital Bed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2307-2016·2016-08-10

    Philips MultiDiagnost Eleva X-Ray System Recalled for Bolt Failure Risk

    Philips is recalling 993 MultiDiagnost Eleva x-ray systems because bolts may break, causing the C-arm to sag. The recall covers units distributed worldwide.

    Product
    MultiDiagnost Eleva; x-ray system. Product Codes: 708032, 708036
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2328-2016·2016-08-10

    Philips IntelliVue Patient Monitor Recall for Outdated Waveform Data

    Philips is recalling IntelliVue Patient Monitors because they may display outdated waveform data if powered on continuously for several months, failing to reflect current patient conditions.

    Product
    IntelliVue Patient Monitor Product Usage: The monitors are indicated for use by health care professionals whenever there is a need for monitoring the physiological parameters of patients. The monitors are intended to be used for monitoring and recording of, and to generate…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2332-2016·2016-08-10

    Stryker Recalls Spirit Select and Plus Hospital Beds Due to Actuator Failure

    Stryker Medical is voluntarily recalling Spirit Select and Spirit Plus hospital beds because broken actuators may cause the bed to lower unexpectedly, risking patient injury.

    Product
    Spirit Select Bed, A-C Powered Hospital Bed
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1454-2016·2016-08-10

    Isomeric Pharmacy Recalls Betamethasone Injectable Suspension Due to Particle Issues

    Isomeric Pharmacy Solution is recalling Betamethasone Acetate / Betamethasone Sodium Phosphate Injectable Suspension due to potential drug clumps and larger particle sizes.

    Product
    Betamethasone Acetate / Betamethasone Sodium Phosphate Injectable Suspension, 7 mg/ mL,10 mL Multi-Dose vial for injection, Rx Only, Isomeric Pharmacy Solution, 2401 Foothill Dr., Salt Lake City, UT 84109
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2308-2016·2016-08-10

    Beckman Coulter Recalls AU480 Chemistry Analyzers Due to Leaking C Cups

    Beckman Coulter is recalling AU480 Chemistry Analyzers because leaking C cups can cause coolant to short-circuit the instrument's circuit boards.

    Product
    AU480 Chemistry Analyzers, Reference No. B28624 The AU series are automated, clinical chemistry analyzers that measure analytes in patient samples (serum, plasma, urine, CSF) in combination with appropriate reagents, calibrators, quality, control (QC) materials, and other…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2310-2016·2016-08-10

    Beckman Coulter AU5800 Chemistry Analyzers Recalled for Leaking C Cups

    Beckman Coulter is recalling AU5800 Chemistry Analyzers because cracked C cups can leak coolant onto circuit boards, causing short-circuits and instrument stop mode.

    Product
    AU5800 Chemistry Analyzers, Reference No. A98352 The AU series are automated, clinical chemistry analyzers that measure analytes in patient samples (serum, plasma, urine, CSF) in combination with appropriate reagents, calibrators, quality, control (QC) materials, and other…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2337-2016·2016-08-10

    Zimmer Air Dermatome II Width Plate Recalled for Surface Coating Defects

    Zimmer Surgical Inc is recalling 90 units of the Air Dermatome II Width Plate because the surface coating is blistering, peeling, and discoloring after use.

    Product
    Zimmer¿ Air Dermatome II Width Plate, 2 inch. Part # 885120200. Width plate is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then…
    Category
    Medical Device
    Distribution
    Distributed nationwide