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.

54601–54625 of 73850

  • CriticalFDA (Drugs)·D-438-2015·2015-04-15

    Central Admixture Pharmacy Services Recalls TPN Neonate Starter Bags for Sterility Issues

    Central Admixture Pharmacy Services is recalling 10 bags of TPN Neonate Starter Bags due to out-of-specification sterility test results indicating microbial contamination.

    Product
    Children's Hospital Colorado Springs TPN Neonate Starter Bag 4% AA/10% DEX, Trophamine 4% Dextrose 10%, compound vol: 500 ml, sterile injectable, Rx only, compounded drug, IV infusion bag packaged in a corrugated box, each container is lined with a polystyrene insert; CAPS…
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0433-2015·2015-04-15

    Hospira Recalls MitoXANTRONE Injection Due to Stability Failures

    Hospira Inc. is recalling MitoXANTRONE Injection vials because the product failed stability specifications, resulting in subpotent medication and out-of-specification impurities.

    Product
    MITOXANTRONE — MITOXANTRONE (MITOXANTRONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-445-2015·2015-04-15

    Central Admixture Pharmacy Services Recalls Compounded TPN Infusion Bags

    Central Admixture Pharmacy Services is recalling 4 bags of compounded TPN infusion bags due to non-sterility test failures.

    Product
    Advocate Good Samaritan Hospital (IL) TPN Dextrose 5% Trophamine 2%, Trophamine 5% Dextrose 2%, compound vol: 250 ml, sterile injectable, Rx only, compounded drug, IV infusion bag packaged in a corrugated box, each container is lined with a polystyrene insert; CAPS, Allentown…
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-447-2015·2015-04-15

    Central Admixture Pharmacy Services Recalls Compounded TPN Bags Due to Sterility Failure

    Central Admixture Pharmacy Services is recalling three bags of compounded TPN due to out-of-specification sterility test results indicating microbial contamination.

    Product
    Methodist Hospital Northlake (IN) Neo Starter TPN D5, AA2, Trophamine 2% Dextrose 5%, Additives: heparin PF 100 units/mL, 50 units/dL, Calcium Gluconate 0.46 mEq/mL, 200 mg/dL, compound vol: 300 ml, sterile injectable, Rx only, compounded drug, IV infusion bag packaged in a…
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-457-2015·2015-04-15

    FDA Recalls Non-Sterile Compounded Neonatal IV Infusion Bags

    Central Admixture Pharmacy Services is recalling 10 bags of compounded neonatal IV solution due to sterility test failures.

    Product
    Hackensack University Med Ctr (NJ) 5% Dextrose Neonatal Solution, Trophamine 3%, Dextrose 5%, Additives: Calcium Gluconate 0.46mEq/mL, 7mEq/L, compound vol: 150 ml, sterile injectable, Rx only, compounded drug, IV infusion bag packaged in a corrugated box, each container is…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-481-2015·2015-04-15

    Baxter Recalls Sodium Chloride Injection Bags Due to Plastic Fragments

    Baxter Healthcare is recalling 542,080 bags of 0.9% Sodium Chloride Injection USP due to confirmed reports of blue plastic fragments from vial adapters.

    Product
    SODIUM CHLORIDE — SODIUM CHLORIDE (SODIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1920-2015·2015-04-15

    Nutiva Coconut Treats Recalled Due to Salmonella Risk

    Nutiva is recalling O'Coconut Lightly Sweetened Coconut Treats because a contract manufacturer found Salmonella in the coconut flakes used to make them.

    Product
    Nutiva O'Coconut Lightly Sweetened Coconut Treat - Classic Sold in 8 - x 0.5 oz. individually wrapped pieces, UPC 6-92752-10557-9 and Singles of 24 - 0.5 oz, per box - UPC 6-92752-10500-5. - 24 singles x 6 caddies per shipping case - 144 individual units. Certified Organic…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0431-2015·2015-04-15

    Navinta Recalls Fomepizole Injection Due to Sterility Assurance Concerns

    Navinta LLC is recalling Fomepizole Injection due to FDA inspection findings of GMP violations that may impact sterility. The recall covers 14,628 units distributed nationwide.

    Product
    Fomepizole Injection, 1.5 g/1.5 mL (1 g/mL), For Intravenous Infusion only, Rx only, Manufactured by: Emcure Pharmaceuticals Lt. for Sandoz Inc., Princeton, NJ 08540, NDC 0781-3182-73 and 0781-3182-84
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1923-2015·2015-04-15

    Talenti Sea Salt Carmel Gelato Recalled for Unlabeled Peanut Ingredient

    Unilever is recalling specific jars of Talenti Sea Salt Carmel Gelato because they may contain peanuts that are not listed on the label.

    Product
    Talenti Gelato & Sorbetto, 1 pt. (473 mL) in clear plastic jars with best by date 5/19/2016, UPC 8685200024
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1921-2015·2015-04-15

    Nutiva Coconut Treats Recalled Due to Salmonella Contamination in Coconut Flakes

    Nutiva is recalling O'Coconut Lightly Sweetened Coconut Treats because desiccated coconut flakes used in the product tested positive for Salmonella.

    Product
    Nutiva O'Coconut Lightly Sweetened Coconut Treat - Hemp & Chia. Sold in Singles of 24 - 0.5 oz, per box - 6-92752-10502-9 24 singles x 6 caddies per shipping case - 144 individual units per case. Certified Organic, Fair Trade Certified. Manufactured for: Nutiva, 213 W.…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1929-2015·2015-04-15

    Classic Cooking Kale and Quinoa Cake Recalled for Undeclared Peanut

    Classic Cooking LLC is recalling Kale and Quinoa Cake because it contains undeclared peanut protein, a major allergen.

    Product
    classic cooking Kale and Quinoa Cake, NET WT. 6.75 lbs. UPC 7-4863-32511-8. KEEP FROZEN.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V223000·2015-04-15

    Chrysler Recalls 2015 Ram ProMaster City for Side Air Bag Defect

    Chrysler is recalling 2015 Ram ProMaster City vehicles because side air bag curtains may not deploy properly, increasing injury risk in crashes.

    Product
    RAM — RAM PROMASTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V225000·2015-04-15

    GM Recalls 2004-2007 Cadillac CTS-V for Brake Hose Corrosion

    General Motors is recalling 2004-2007 Cadillac CTS-V vehicles in specific states because front brake hose fittings may corrode, potentially causing brake leaks and increased stopping distance.

    Product
    CADILLAC — CADILLAC CTS-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0483-2015·2015-04-15

    Hospira Recalls Ketorolac Tromethamine Injections Due to Crystallization

    Hospira Inc. is voluntarily recalling specific lots of Ketorolac Tromethamine Injection due to crystallization. The recall covers vials distributed nationwide and internationally.

    Product
    KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·15V222000·2015-04-15

    Chrysler Recalls 2006 Dodge Viper and Jeep Models for Clutch Defect

    Chrysler is recalling 2006 Dodge Viper and Jeep Wrangler/Liberty vehicles because a broken clutch pedal spring may cause the vehicle to lurch unexpectedly, increasing crash risk.

    Product
    DODGE — DODGE, JEEP VIPER COUPE, LIBERTY, WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15728·2015-04-15

    Cycle Gear Recalls Wheelies Toys Due to Excessive Lead Levels

    Cycle Gear is recalling Wheelies semi-truck and motorcycle toys because they contain excessive lead levels, violating federal standards.

    Product
    Wheelies semi-truck with six motorcycles and push-along motorcycle with rider.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15110·2015-04-15

    Husky Vertical Bike Hooks Recalled Due to Risk of Injury

    Waterloo Industries is recalling Husky Securelock Vertical Bike Hooks because they can detach and fall, posing a risk of injury to bystanders.

    Product
    Husky® Securelock™ Vertical Bike Hooks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1397-2015·2015-04-15

    CooperSurgical Infant Transport Mattress Recalled for Missing Expiration Date

    CooperSurgical is recalling TransWarmer Infant Transport Mattresses because they lack expiration dates, potentially failing to meet specifications.

    Product
    CooperSurgical TransWarmer Infant Transport Mattress with WarmGel P/N 20421 Private label: NovaPlus TransWarmer Infant Heat Therapy Mattress with WarmGel. P/N V6390 Provides warmth during transport of infant within the hospital or between hospitals
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1942-2015·2015-04-15

    Vitarroz Sazon Seasoning Recalled for Undeclared Peanut Protein

    Iberia Foods is recalling Vitarroz Sazon seasoning packets because the cumin ingredient may contain undeclared peanut protein.

    Product
    VITARROZ SAZON CON CULANTRO Y ACHIOTE CORIANDER & ANNATTO, NET WT. 6.34 OZ. 180g, Jumbo SOBRES 36 PACKETS, UPC 0 72670 04255 0.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0482-2015·2015-04-15

    Hospira Recalls Ketorolac Tromethamine Injection Due to Crystallization

    Hospira Inc. is voluntarily recalling specific lots of Ketorolac Tromethamine Injection because of crystallization. The affected vials were distributed nationwide and in Guam and Singapore.

    Product
    KETOROLAC TROMETHAMINE — KETOROLAC TROMETHAMINE (KETOROLAC TROMETHAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1941-2015·2015-04-15

    Iberia Sazon Seasoning Recalled for Undeclared Peanut Protein

    Iberia Foods is recalling Sazon Iberia seasoning because it may contain undeclared peanut protein. Consumers should check lot numbers and stop using the product.

    Product
    SAZON IBERIA CON CULANTRO Y ACHIOTE Coriander & Annatto: 1) NET WT. 3.52 OZ. 100g, 18/20 PACKS, UPC 0 75669 10832 9, 2) NET WT. 6.34 OZ. 180g, 15/36 PACKS, UPC 0 75669 10831 2
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1394-2015·2015-04-15

    Toshiba INFX-8000V Interventional Angiography System Recall for Brake Defect

    Toshiba is recalling 28 INFX-8000V Interventional Angiography Systems because the table base rotational brake may not engage when force is applied to the table top.

    Product
    INFX-8000V Interventional Angiography System. CAT-880B catheterization table. Cardiac and Vascular intervention with fluoroscopic and fluorographic images. For the USA and Canada the system is registered as lnfinix CF-i or lnfinix VF-i, for national regulations. INFX-8000V…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15V224000·2015-04-15

    Thor Motor Coach Recalls 2016 Motorhomes for Missing Weight Label

    Thor Motor Coach is recalling 168 model year 2016 motorhomes because the Occupant and Cargo Carrying Capacity label may be missing water weight information, creating an overload risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH, THOR MOTOR CHATEAU, OUTLAW, CITATION, SIESTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1408-2015·2015-04-15

    VasoNova Vascular Positioning System G4 Console Recalled for Standard Noncompliance

    VasoNova is recalling 17 Vascular Positioning System G4 Consoles due to noncompliance with IEC Standard 60101-1-1.

    Product
    VasoNova Vascular Positioning System (VPS ) G4 Console Catalog number VPS-G4C Cardiovascular: The VPS Stylet and Console are indicated for guidance and tip positioning for central venous catheters.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1379-2015·2015-04-15

    TEM Systems Recalls ROTROL P Control Vials Due to Partial Filling

    TEM Systems Inc is recalling specific lots of ROTROL P Control vials because some were found to be partially filled.

    Product
    ROTROL P Control for ROTEM delta Thromboelastometry System, Manufactured for: Tem Innovations GmbH.
    Category
    Medical Device
    Distribution
    Distributed nationwide