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.

55326–55350 of 73850

  • SevereFDA (Devices)·Z-1054-2015·2015-02-11

    Cardinal Health Recalls Lubricated Intubating Stylets Due to Shear Risk

    Cardinal Health is recalling 104,432 Lubricated Intubating Stylets 6FR because a small piece of the sheath may shear off during removal, posing a risk to infants and pediatric patients.

    Product
    Lubricated Intubating Stylet 6FR that is inserted into an endotracheal tube to facilitate intubation. This product is used in surgical or medical emergency facilities. Primarily used on infants and pediatric patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1017-2015·2015-02-11

    FDA Recalls Covidien Trellis-6 Peripheral Infusion Systems Due to Labeling Error

    The FDA is recalling 216 units of the Covidien Trellis-6 Peripheral Infusion System because a manufacturing error caused the balloon inflation ports to be incorrectly labeled.

    Product
    Covidien Trellis-6 Peripheral Infusion System. Models BVT608010V01, BVT608030V01, BVT612010V01, and BVT612030V01. Sterile EO. Product Usage: Intended for controlled and selective infusion of physician-specified fluids, including thrombolytics, into the peripheral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0958-2015·2015-02-11

    Reily Foods Recalls Chili Kits for Undeclared Peanut and Almond Allergens

    Reily Foods is recalling Wick Fowler's Famous Texas Style 2-Alarm Chili Kits because they contain peanut and almond allergens that are not declared on the ingredient statements.

    Product
    WICK FOWLER'S FAMOUS TEXAS STYLE 2-ALARM Chili Kit, NET WT. 3.6525 oz. (102g), Dist. by Reily Foods Company, New Orleans, LA 70130, 1-800-535-1961, UPC 0-00-71092-00069-8
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0956-2015·2015-02-11

    Reily Foods Recalls Chili Kits With Undeclared Peanut and Almond Allergens

    Reily Foods is recalling Carroll Shelby's Original Texas Brand Chili Kits because they contain peanut and almond allergens not listed on the ingredient label.

    Product
    CARROLL SHELBY'S ORIGINAL TEXAS BRAND CHILI KIT, NET WT. 4 oz. (113 g), Dist. by Reily Foods Company, New Orleans, LA 70130, 1-800-535-1961, UPC 0-00-72396-10000-8
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V086000·2015-02-11

    Airstream Recalls 2014-2015 Travel Trailers Due to Propane Tank Screw Failure

    Airstream is recalling 2014-2015 travel trailers because screws securing the propane tank tray may fail, allowing tanks to fall and cause fire or collision.

    Product
    AIRSTREAM — AIRSTREAM FLYING CLOUD, INTERNATIONAL, LAND YACHT, SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1018-2015·2015-02-11

    FDA Recalls Covidien Trellis-8 Peripheral Infusion Systems Due to Labeling Error

    FDA is recalling 1,032 units of the Covidien Trellis-8 Peripheral Infusion System because a manufacturing error caused the proximal and distal balloon inflation ports to be incorrectly labeled.

    Product
    Covidien Trellis-8 Peripheral Infusion System. Models CVT808015, CVT808025, CVT812015, and CVT812025. The following models are not offered for sale in the US: EVT808015, EVT808025, EVT812015, and EVT812025 Sterile EO. Product Usage: Intended for controlled and selective…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0957-2015·2015-02-11

    Reily Foods Recalls White Chicken Chili Kits Due to Undeclared Allergens

    Reily Foods is recalling Carroll Shelby's Original Texas Brand White Chicken Chili Kits because they contain peanut and almond allergens not listed on the ingredient label.

    Product
    CARROLL SHELBY'S ORIGINAL TEXAS BRAND WHITE CHICKEN CHILI KIT, 3 oz. (85 g), Dist. by Reily Foods Company, New Orleans, LA 70130, UPC 0-00-72396-10019-0
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0959-2015·2015-02-11

    Reily Foods Recalls Wick Fowler's Chili Kits for Undeclared Allergens

    Reily Foods is recalling Wick Fowler's Texas Style False Alarm Mild Chili Kits because they contain peanut and almond allergens that are not declared on the ingredient statements.

    Product
    WICK FOWLER'S TEXAS STYLE FALSE ALARM Mild Chili Kit, NET WT. 3.03 oz. (86g), Dist. by Reily Foods Company, New Orleans, LA 70130, UPC 0-00-71092-00111-4
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0382-2015·2015-02-11

    Hospira Recalls Lidocaine Hydrochloride Injection Due to Particulate Matter

    Hospira Inc. is recalling 120,900 vials of 1% Lidocaine Hydrochloride Injection because iron oxide particulates were found in the solution.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1036-2015·2015-02-11

    Invacare Recalls G-Series Bed Rails Due to Entrapment Safety Defect

    Invacare is recalling G-Series bed rails because the mounting bracket does not meet entrapment safety specifications.

    Product
    G- Series Beds; G29 full length bed rails assembly
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1042-2015·2015-02-11

    Zimmer Persona Tibial Inserter Recalled for Potential Tip Fracture

    Zimmer, Inc. is recalling 1,091 Persona Tibial Articular Surface Inserters due to a potential fracture of the instrument tip, which could cause tissue damage or require revision surgery.

    Product
    Zimmer PERSONA Tibial Articular Surface Inserter; Item # 42-5299-001-00. Manual surgical instrument for knee arthroplasty (orthopedic).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15077·2015-02-11

    System Sensor Recalls Combination Carbon Monoxide and Smoke Detectors

    System Sensor is recalling i4 Series combination CO/smoke detectors because they may fail to detect carbon monoxide, posing a poisoning risk.

    Product
    i4 Series System Sensor combination carbon monoxide (CO)/smoke detectors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1038-2015·2015-02-11

    SCC Soft Computer Recalls SoftLab Laboratory Information System Versions

    SCC Soft Computer is recalling SoftLab versions 4.0.7.0 and 4.0.7.1 because the software fails to send abnormal flags for Reference Lab test results.

    Product
    SoftLab with SA HIS versions 4.0.7.0-4.0.7.1 SoftLab is a laboratory information system to be used in a medical research or clinical laboratory.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0972-2015·2015-02-11

    Zilks Foods Recalls Green Chili Hummus Due to Undeclared Peanuts

    Zilks Foods is recalling 3,176 cups of Green Chili Hummus because the cumin ingredient may contain undeclared peanuts.

    Product
    Hummus; All-natural ZILKS HATCH GREEN CHILI HUMMUS GLUTEN FREE & NON-GMO NET WT. 8 OZ
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0971-2015·2015-02-11

    Zilks Foods Recalls Balsamic and Garlic Hummus for Undeclared Peanuts

    Zilks Foods is recalling 2,424 cups of Balsamic and Garlic Hummus due to potential undeclared peanuts in the cumin ingredient.

    Product
    Hummus; All-natural ZILKS BALSAMIC & GARLIC HUMMUS GLUTEN FREE & NON-GMO NET WT. 8 OZ
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0973-2015·2015-02-11

    Zilks Spinach and Artichoke Hummus Recalled for Undeclared Peanuts

    Zilks Foods is recalling Spinach & Artichoke Hummus because the cumin ingredient may contain undeclared peanuts.

    Product
    Hummus; All-natural ZILKS SPINACH & ARTICHOKE HUMMUS GLUTEN FREE & NON-GMO NET WT. 8 OZ
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1049-2015·2015-02-11

    Carl Zeiss Meditec FORUM Archive and Viewer Software Recall

    Carl Zeiss Meditec is recalling FORUM Archive and Viewer software versions 3.1 and 3.2 due to a defect that may lead to misinterpretation of optical coherence tomography data.

    Product
    FORUM Archive and Viewer, version 3.1, v 3.1.1, (DVD Format) and v 3.2, v 3.2.1.(DVD and USB Flash Drive Format). Catalog numbers: 000000-20107-750 (DVD with either FORUM v 3.1 or v 3.1.1) 000000-2058-601 (DVD with either FORUM v 3.2 or 3.2.1); 000000-2084-928 (USB drive…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1039-2015·2015-02-11

    Baxter Integrated APD Set Recalled for Leakage Complaints

    Baxter Healthcare is recalling 8,640 units of Integrated APD Sets with Cassette 3-Prong due to leakage complaints. The sterile fluid path is used for peritoneal dialysis.

    Product
    Baxter Integrated APD Set with Cassette 3-Prong, Sterile, nonpyrogenic fluid path. Product Usage: The recall device is indicated for use in the treatment of patients with renal failure to provide PD fluid exchanges with Baxter HomeChoice PD Systems in clinical and home use…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1040-2015·2015-02-11

    Sedecal MobileDiagnost wDR X-ray systems recalled for unexpected movement

    Sedecal S.A. is recalling 283 MobileDiagnost wDR motorized portable diagnostic X-ray systems due to reports of unexpected movement.

    Product
    MobileDiagnost wDR motorized portable diagnostic X-ray systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0969-2015·2015-02-11

    Zilks Roasted Red Pepper Hummus Recalled for Undeclared Peanuts

    Zilks Foods is recalling 4,008 cups of Roasted Red Pepper Hummus due to potential undeclared peanuts in the cumin ingredient.

    Product
    Hummus; All-natural ZILKS ROASTED RED PEPPER HUMMUS GLUTEN FREE & NON-GMO NET WT. 8 OZ
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1055-2015·2015-02-11

    BD 10 mL Syringes Recalled Due to Improperly Seated Stopper

    Becton Dickinson is recalling 564,000 units of 10 mL syringes because the stopper is not properly seated in the syringe.

    Product
    BD 10 mL Syringe BD Luer-Lok Tip with Blunt Plastic Cannula, Not for Skin Injection ; Catalog #303348, BD 10 mL Syringe Luer-Lok Tip with Blunt Fill Needle 18G x 1 1/2 (1.2mm x 40 mm), not for skin injection; Catalog #305064 BD 10 mL Syringe Luer-Lok Tip with BD…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0968-2015·2015-02-11

    Zilks Hummus Recalled for Potential Undeclared Peanuts

    Zilks Foods is recalling 4,768 cups of hummus nationwide due to potential undeclared peanuts in the cumin ingredient.

    Product
    Hummus; All-natural ZILKS FAMOUS ORIGINAL HUMMUS GLUTEN FREE & NON-GMO NET WT. 8 OZ
    Category
    Food
    Distribution
    Distributed nationwide