The Recall Desk

State

Northern Mariana Islands product recalls

73,478 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 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22976–23000 of 73501

  • HighFDA (Food)·F-0032-2022·2021-10-27

    Chocolate & the Chip Maple Macadamia Cookies recalled for undeclared allergens

    Chocolate & the Chip Maple Macadamia Cookies contain undeclared allergens including wheat, milk, soy, and tree nuts that were not properly disclosed on product labels.

    Product
    Chocolate & the Chip Maple Macadamia Cookies: 4 oz / 114 grams per pack. Cookies are packaged in uniform pairs in a food grade clear resealable bag and label Corrected Ingredients: All purpose flour (bleached wheat flour, malted barley flour, niacin, reduced iron, ascorbic…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0150-2022·2021-10-27

    Anti-Xa Assay On-Board Stability Reduced from 7 to 5 Days

    The HemosIL Liquid Anti-Xa diagnostic assay has reduced on-board stability from 7 days to 5 days. Laboratories should follow updated stability guidelines for all currently released and future lots.

    Product
    HemosIL Liquid Anti-Xa- automated chromogenic assay for in vitro diagnostic use by laboratory professionals in clinical laboratories. The assay provides quantitative results on 3.2% citrated human plasma Part Number: 0020302602
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0160-2022·2021-10-27

    Bone Screw Labeling Error: Actual Length May Not Match Package Label

    Limacorporate is recalling bone screws (REF 8420.15.010) because the actual length of the screws may not correspond to the length stated on the package label, potentially affecting proper surgical placement and implant stability.

    Product
    REF 8420.15.010, Bone Screw/Vite - Ti6AI4V, Self Tapping/Autofilettante, Dia=6.5mm, h=20mm, STERILE R, 2100099, UDI: (01)08033390018845
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0046-2022·2021-10-27

    Chocolate & the Chip Gluten-Free Cookie Cake Recalled for Undeclared Tree Nuts

    Chocolate & the Chip is recalling its gluten-free cookie cake due to undeclared tree nuts (hazelnuts and almonds) found on the packaging labels. The product was distributed nationwide and poses a risk to consumers with tree nut allergies.

    Product
    Chocolate & the Chip Gluten free cookie cake: Cookie cakes: 1LB 1.4oz / 494 grams Packaged in a brown bakery box with window and labeled.1 unit per package. Corrected Ingredients: Not provided Labels found during the inspection had undeclared tree nuts (hazelnuts and…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0052-2022·2021-10-27

    Rice Crispy Treats Recalled for Undeclared Milk and Soy Allergens

    Chocolate & the Chip is recalling The Sweetie Rice Crispy treats due to undeclared milk and soy allergens found during inspection. The products were distributed nationwide.

    Product
    Chocolate & the Chip The Sweetie Rice Crispy: Rice crispy treats: 6 oz / 171 grams Packaged in a food grade clear poly tubing, heat sealed with label Corrected Ingredients: Not provided Labels found during the inspection had undeclared milk, soy. Firm had listed…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0158-2022·2021-10-27

    Medtronic surgical blades recalled for tip breaks and vibration

    Medtronic recalls 274,991 sterile surgical blades due to complaints of tip breaks and vibration during use. The blades are components of surgical systems used in brain and ENT procedures.

    Product
    Medtronic Sterile single-use blades that are components of the StraightShot M Series Handpiece and Fusion ENT Navigation Software, and the Midas Rex Microsaw and Triton System with the following product numbers: (1) REF 40A2500, Nucleus Removal Angled Blade, 25 cm x 4.0 mm…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·22011·2021-10-27

    Magnussen Home Nova Series 5-Drawer Chests Recalled for Tip-Over Hazard

    Magnussen Home is recalling about 13,200 Nova Series 5-Drawer Chests sold from August 2009 through August 2015 because they can tip over and cause entrapment hazards to children if not anchored to the wall.

    Product
    Nova Series 5-Drawer Chests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0050-2022·2021-10-27

    Chocolate & the Chip Brown Butter Rice Crispy Treats Recalled for Undeclared Milk

    Chocolate and the Chip is recalling Brown Butter Rice Crispy Treat products due to undeclared milk allergen on labels. The products were distributed nationwide and manufactured between July 1 and September 30, 2021.

    Product
    Chocolate & the Chip Brown Butter Rice Crispy Treat - Chocolate: Rice crispy treats: 6 oz / 171 grams Packaged in a food grade clear poly tubing, heat sealed with label Corrected Ingredients: Ingredients: rice cereal (rice, sugar, malt extract, salt, preservative…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V840000·2021-10-27

    Hyundai recalls 2021 Palisade for brake fluid contamination

    Brake fluid contamination in certain 2021 Hyundai Palisades can reduce braking performance and increase crash risk. Owners should contact Hyundai for a free brake system repair.

    Product
    HYUNDAI — HYUNDAI PALISADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22010·2021-10-27

    Liberty Hardware Glass Cabinet Knobs Recalled for Laceration Hazard

    Liberty Hardware is recalling about 38,000 glass cabinet knobs because the glass stem can break during use, causing laceration injuries. Consumers should stop using the knobs and contact Liberty Hardware for a refund.

    Product
    Glass cabinet knobs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0028-2022·2021-10-27

    Chocolate & the Chip Cookies Recalled for Undeclared Allergens

    Chocolate & the Chip Original Cookies are being recalled due to undeclared allergens including wheat, milk, soy, and tree nuts (hazelnuts) found during a California Department of Public Health inspection. Consumers with allergies to these substances should not consume the product.

    Product
    Chocolate & the Chip The Original Cookies: 4 oz / 114 grams per pack. Cookies are packaged in uniform pairs in a food grade clear resealable bag and label Corrected Ingredients: Original chocolate chip cookie: Ingredients: All purpose flour (bleached wheat flour, malted barley…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0033-2022·2021-10-27

    Chocolate & the Chip Cookies Recalled for Undeclared Allergens

    Chocolate & the Chip is recalling Fluffadoodle and Fluffa-Nutta Cookies due to undeclared wheat, milk, and soy allergens found on packaging labels during a California health inspection.

    Product
    Chocolate & the Chip Fluffadoodle and Fluffa-Nutta Cookies: 4 oz / 114 grams per pack. Cookies are packaged in uniform pairs in a food grade clear resealable bag and label Corrected Ingredients: Ingredients: All purpose flour (bleached wheat flour, malted barley flour…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0036-2022·2021-10-27

    Chocolate & the Chip Octoberfest Cookies Recalled for Undeclared Allergens

    Chocolate & the Chip Octoberfest Cookies are being recalled due to undeclared wheat, milk, and soy allergens found on product labels during a California Department of Public Health inspection.

    Product
    Chocolate & the Chip Octoberfest Cookies: 4 oz / 114 grams per pack. Cookies are packaged in uniform pairs in a food grade clear resealable bag and label Corrected Ingredients: Not provided. Labels found during the inspection had undeclared wheat, milk, soy. Firm had listed…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0042-2022·2021-10-27

    Chocolate & the Chip Lavender Cookies Recalled for Undeclared Allergens

    Chocolate & the Chip is recalling Lavender chocolate chip cookies due to undeclared wheat, milk, and soy allergens found on product labels during a California Department of Public Health inspection.

    Product
    Chocolate & the Chip Lavender chocolate chip cookies: Cookies: 4 oz / 114 grams per pack. Cookies are packaged in uniform pairs in a food grade clear resealable bag and label Corrected Ingredients: Ingredients: All purpose flour (bleached wheat flour, malted barley flour…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0015-2022·2021-10-27

    Coppertone Pure & Simple 50 Sunscreen Spray Recall for cGMP Deviations

    Beiersdorf Inc. is recalling Coppertone Pure & Simple 50 Sunscreen Spray due to manufacturing practice deviations. Approximately 36,660 cans were distributed nationwide.

    Product
    Coppertone Pure & Simple 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02880 0
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0019-2022·2021-10-27

    Rocuronium Bromide Injection Lacks Paralyzing Agent Warning

    Piramal Critical Care is recalling Rocuronium Bromide Injection because the finished product vial lacks the required "WARNING: PARALYZING AGENT" statement on the flip cap. The missing warning could lead to unsafe use of this prescription neuromuscular-blocking drug.

    Product
    Rocuronium Bromide Injection 50mg/5 mL, 5mL Multi-Dose Vial, Rx only, Manufactured for: Piramal Critical Care, Bethlehem, PA 18017, USA, Manufactured by: Sanovel Ilac, San. Ve Tic. A.S. Istanbul, Turkey, NDC 66794-0228-41
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0120-2022·2021-10-27

    Diagnostic Control Material Outside Expected Range, Potential for Delayed Results

    Ortho Clinical Diagnostics is recalling VITROS Anti-SARS-CoV-2 Immunodiagnostic Controls that may be outside the expected control range, potentially delaying diagnostic test results in laboratory systems.

    Product
    VITROS Immunodiagnostic Products Anti-SARS-CoV-2 IgG Quantitative Controls (IVD)- For use in monitoring the performance of the VITROS ECi/ECiQ/3600 Immunodiagnostic Systems and the VITROS 5600/XT 7600 Integrated Systems when used with the VITROS Immunodiagnostic Products…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0022-2022·2021-10-27

    AirDuo Digihaler 232/14 Inhalation Powder Subpotent Recall

    Teva Pharmaceuticals is recalling AirDuo Digihaler 232/14 inhalation powder because some units do not deliver the correct amount of salmeterol as labeled.

    Product
    AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14 mcg) Inhalation Powder, Sample Not For Sale, Rx Only, Mktd by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-530-08.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0025-2022·2021-10-27

    AirDuo Digihaler 232/14 Inhalation Powder Recall for Subpotent Salmeterol

    Teva Pharmaceuticals is recalling approximately 5,500 units of AirDuo Digihaler 232/14 inhalation powder distributed nationwide because some inhalers contain less salmeterol than the labeled dose.

    Product
    AirDuo Digihaler 232/14 (fluticasone propionate 232 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-136-06
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0143-2022·2021-10-27

    Smith & Nephew cannulated screw label incorrectly indicates threading type

    Smith & Nephew is recalling 6.5mm x 165mm cannulated screws because the product label incorrectly states the screws are fully threaded when they are actually partially threaded.

    Product
    6.5MMX165MM CANNULATED SCREW
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0017-2022·2021-10-27

    Coppertone Pure & Simple Baby 50 Sunscreen Spray Recalled for cGMP Deviations

    Beiersdorf Inc. is recalling 14,748 cans of Coppertone Pure & Simple baby 50 Sunscreen Spray due to cGMP (current Good Manufacturing Practice) deviations. The product was distributed nationwide.

    Product
    Coppertone Pure & Simple baby 50 Sunscreen Spray (To Deliver) Zinc Oxide 24.08%, NET WT 5 OZ (142 g) can, Beiersdorf Inc., Wilton, CT 06897 UPC 0 72140 02881 7
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0026-2022·2021-10-27

    Omeprazole Magnesium Acid Reducer Capsules Recalled for Staple Contamination

    Dr. Reddy's Laboratories is recalling Acid Reducer (Omeprazole Magnesium) 20 mg capsules nationwide because staples have been found co-mingled with capsules in bottles.

    Product
    ACID REDUCER — ACID REDUCER (OMEPRAZOLE MAGNESIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0024-2022·2021-10-27

    AirDuo Digihaler inhalation powder subpotent drug recall

    Teva Pharmaceuticals is recalling AirDuo Digihaler 113/14 inhalation powder because some batches do not deliver the labeled amount of salmeterol, a critical active ingredient for asthma and COPD control.

    Product
    AirDuo Digihaler 113/14 (fluticasone propionate 113 mcg and salmeterol 14 mcg) Inhalation Powder, Rx Only, Mktd. by: Teva Respiratory, LLC, Frazer, PA 19355, Manufactured in Ireland, NDC 59310-129-06.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0151-2022·2021-10-27

    HemosIL Liquid Anti-Xa Assay On-Board Stability Issue Recall

    Instrumentation Laboratory is recalling HemosIL Liquid Anti-Xa, a coagulation assay measuring heparin activity, due to reduced on-board instrument stability from 7 days to 5 days.

    Product
    HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative determination of unfractionated heparin (UFH) and low molecular weight heparin (LMWH) activity in human citrated plasma on IL Coagulation Systems, (ACLTOP¿ Family, ACL TOP Family 50 Seriest and ACL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0149-2022·2021-10-27

    Heparin Activity Assay Labeling Correction: Reduced On-Board Stability

    Instrumentation Laboratory is recalling HemosIL Liquid Anti-Xa kits due to a labeling correction. The on-board stability window has been reduced from 7 to 5 days.

    Product
    HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative determination of unfractionated heparin (UFH) and low molecular weight heparin (LMWH) activity in human citrated plasma on IL Coagulation Systems, (ACL TOP¿ Family, ACL TOP Family 50 Seriest and ACL…
    Category
    Medical Device
    Distribution
    Distributed nationwide