The Recall Desk

State

Northern Mariana Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58676–58700 of 73856

  • HighFDA (Food)·F-1747-2014·2014-04-16

    Northern Valley Baking Recalls G'nache P'nache for Undeclared Milk and Soy

    Northern Valley Baking Co. is recalling G'nache P'nache products because milk and soy were not declared on the allergen statement.

    Product
    The Other Macaroon G'nache P'nache 5.3 oz. Manufactured and Distributed by:Northern Valley Baking Co LLC, Dumont, New Jersey USA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1452-2014·2014-04-16

    Draeger Recalls Reusable Latex Breathing Bags Due to Allergic Reaction Incident

    Draeger Medical is recalling reusable latex breathing bags and test lungs after a user reported an acute allergic reaction. The product is distributed nationwide.

    Product
    Reusable latex breathing bags with multiple part numbers and sold as part of test lung part number and reusable anaesthesia sets. Product Usage: The breathing bag is a component of the anesthesia set (breathing circuit) that is intended to is the conduit for administering…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1450-2014·2014-04-16

    Medcare Floor Lifts Recalled Due to Potential Pin Failure

    ErgoSafe Product LLC is recalling Medcare Floor Lifts manufactured between 2010 and 2012 because a design pin may break over time.

    Product
    400003 Medcare Lift with Scale 400013 Medcare Lift w/Scale 600 lb 400600 Scale Hanger Assembly Product Usage: The intended use is a patient hanger bar (400600) attached to a 400003 or 400013 floor lift used to lift, transfer or position clients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1752-2014·2014-04-16

    Keen-Wah Quinoa Clusters Recalled for Undeclared Soy Allergen

    Keen-Wah LLC is recalling i heart keenwah Cranberry Cashew Quinoa Clusters because soy lecithin was used in manufacturing but not declared on the label.

    Product
    i heart keenwah Cranberry Cashew All Natural Quinoa Clusters. UPC 736211802545 for the 4 oz UPC 713757598309 for the 1 oz
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1751-2014·2014-04-16

    Keen-Wah Quinoa Clusters Recalled for Undeclared Soy Allergen

    Keen-Wah LLC is recalling i heart keenwah Ginger Peanut All Natural Quinoa Clusters because an anti-stick spray containing soy lecithin was used during manufacturing, but soy was not declared on the label.

    Product
    i heart keenwah Ginger Peanut All Natural Quinoa Clusters. UPC 736211802644 for the 4 oz UPC 713757598408 for the 1 oz
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1444-2014·2014-04-16

    Smiths Medical HOTLINE Fluid Warming Set Recall for Injection Port Leaks

    Smiths Medical is recalling HOTLINE Fluid Warming Sets because the injection port septum may leak or become dislodged.

    Product
    Smiths Medical HOTLINE¿ Fluid Warming Set L-80. Product Usage: intended for the delivery of warmed blood and intravenous fluids at normothermic temperatures under gravity conditions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1443-2014·2014-04-16

    Smiths Medical HOTLINE Fluid Warming Set Recall for Injection Port Leaks

    Smiths Medical is recalling HOTLINE Fluid Warming Sets because the injection port septum may leak or become dislodged, potentially causing blood or IV fluid leaks.

    Product
    Smiths Medical HOTLINE¿ Fluid Warming Set L-70. Product Usage: intended for the delivery of warmed blood and intravenous fluids at normothermic temperatures under gravity conditions
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1437-2014·2014-04-16

    DePuy Shoulder Guide Pin Recall Due to Breakage Risk

    DePuy Orthopaedics is recalling 21,675 GLOBAL Anchor Peg Glenoid Plus 2.5mm Breakaway Guide Pins because they may break and be left in patients during surgery.

    Product
    GLOBAL¿ Anchor Peg Glenoid Plus (APG+) 2.5MM Breakaway Guide Pin Part # 2230-00-019, Non-Sterile, DePuy, Johnson & Johnson Product Usage: Usage: The GLOBAL APG+ 2.5mm Guide Pin is a single-use instrument that is used to assist the surgeon in the orientation of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V197000·2014-04-16

    Cummings recalls wheelchair lifts on Ford and Chevrolet vans

    Cummings Mobility is recalling wheelchair lifts on certain Ford and Chevrolet vans because roll stop latches may bend, posing a fall risk.

    Product
    FORD — FORD, CHEVROLET E-350, C5500, G3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1447-2014·2014-04-16

    Breg Recalls Knee Supports for Missing Latex Warning Labels

    Breg Inc is recalling two knee support models because they contain latex but lack the required caution label.

    Product
    K-Lite Knee 2 Stays with Visco, Model No. 122015. Product Usage: The product is intended to provide flexible knee support.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V193000·2014-04-16

    Wheeled Coach Recalls Ambulances Due to Electrical Timer Power Loss

    Wheeled Coach is recalling specific ambulances because an electrical timer may lose power, potentially cutting electricity to the patient area and increasing injury risk.

    Product
    WHEELED COACH — WHEELED COACH AMBULANCE-M2 CHASSIS, T3, T2, T1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1753-2014·2014-04-16

    Keen-Wah Quinoa Clusters Recalled for Undeclared Soy Allergen

    Keen-Wah LLC is recalling i heart keenwah Peanut Butter Cacao All Natural Quinoa Clusters because an anti-stick spray containing soy lecithin was used during manufacture, and soy was not declared on the label.

    Product
    i heart keenwah Peanut Butter Cacao All Natural Quinoa Clusters. UPC 736211884442 - 4 oz 12 units/cs
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1198-2014·2014-04-16

    Terra-Medica Recalls Pleo Not Portable Sips Due to Penicillin Contamination

    Terra-Medica Inc. is recalling specific batches of Pleo Not Portable Sips oral homeopathic medicine due to penicillin cross-contamination.

    Product
    Pleo Not PORTABLE SIPS 7X,10 x 1 mL Cartons, Oral Homeopathic Medicine, OTC Only. Made in Germany, Distributed by: SANUM USA Corp., 1465 Slater Road, Ferndale, WA 98248. Manufactured by: Sanum-Kehlbeck GmbH & Co. KG. NDC: 49807-2310-1. Pleo Not PORTABLE SIPS 7X, 50 x 1 mL…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·14V194000·2014-04-16

    Free Spirit Recreational Vehicles Recalled for Trailer Wiring Defect

    Triple E Recreational Vehicles is recalling 2012-2014 Free Spirit models because trailer hazard lights may not work when the RV ignition is off.

    Product
    FREE SPIRIT — FREE SPIRIT FS22SS, FS22, FS22TE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1193-2014·2014-04-16

    Terra-Medica Recalls Pleo Not Capsules Due to Penicillin Cross Contamination

    Terra-Medica Inc. is recalling Pleo Not Capsules 4X because of penicillin cross contamination. The product was distributed in the US, Canada, and the Philippines.

    Product
    Pleo Not CAPSULES 4X, 20 Tablet Cartons, Oral Homeopathic Fever Reducer/ Cough Suppressant/ Decongestant Medicine, OTC Only. Made in Germany, Distributed by: SANUM USA Corp.,1465 Slater Road, Fernadale, WA 98248; Manufactured By: SANUM-Kehlbeck GmbH & Co. KG. NDC: 49807-2303-1.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1225-2014·2014-04-16

    Agila Recalls Etomidate Injection Due to Particulate Matter and Labeling Issues

    Agila Specialties Private Ltd. is recalling etomidate injection vials due to potential particulate matter and missing or illegible lot and expiry date labels.

    Product
    etomidate injection, USP, 2 mg/mL, packaged in a) 20 mg/10 mL (2 mg/mL), 10 mL Single Dose Vials (NDC 0069-0006-02), 10 x 10 mL vials per carton (NDC 0069-0006-01) and b) 40 mg/20 mL (2 mg/mL) 20 mL Single Dose Vials (NDC 0069-0006-04), 10 x 20 mL vials per carton (NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1441-2014·2014-04-16

    Remington Medical Recalls FAS-LOC Extension Cables Due to Labeling Error

    Remington Medical is recalling FAS-LOC 6 Foot Disposable Extension Cables because the instruction manual incorrectly displays the polarity for the black connector.

    Product
    FAS-LOC 6 Foot Disposable Extension Cable with Safe Connect/Screw Down. Electrical extension cable intended to transmit signal from, or power or excitation signal to patient connected electrodes. The cable is a sterile, disposable device.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1756-2014·2014-04-16

    Smiley National Recalls Kratom Products Due to Unapproved Dietary Ingredients

    Smiley National is voluntarily recalling specific Kratom products because they contain unapproved dietary ingredients.

    Product
    Enhanced Maeng Da Leaf Powder, Maeng Da Kratom, capsule, UPC code 5410600330, 10 Pack, 2 Servings Per Pack, 10 grams.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1449-2014·2014-04-16

    Roche Cobas c502 Analyzer Recall Due to Inactive Volume Check

    Roche Diagnostics is recalling 76 Cobas c502 clinical chemistry analyzers because the Initial Cassette Volume Check feature fails to activate when specific reagent packs are loaded.

    Product
    Cobas c8000 Modular Analyzer Series Cobas c502, Part Number 5964067001, a clinical chemistry analyzer intended for the in vitro quantitative / qualitative determination of analytes in body fluids.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1757-2014·2014-04-16

    Smiley National Recalls Kratom Supplements Due to Unapproved Ingredients

    Smiley National is voluntarily recalling specific Kratom herbal dietary supplements because they contain unapproved dietary ingredients.

    Product
    All Natural, XL Kratom, Herbal Dietary Supplement, capsule, UPC code 5410600307, 4 capsules per package.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1755-2014·2014-04-16

    Smiley National Recalls Kratom Supplements Due to Unapproved Ingredients

    Smiley National is voluntarily recalling specific Kratom herbal dietary supplements because they contain unapproved dietary ingredients.

    Product
    Enhanced Bali Leaf Powder, Max Kratom, Capsule, UPC Code 5410600332, 20 count pack, 5 servings per pack, Herbal Dietary Supplement.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1436-2014·2014-04-16

    Clinical Diagnostic Solutions Recalls Hematology Control Material Due to Elevated MCV

    Clinical Diagnostic Solutions is recalling Boule Con-Diff Tri-Level Hematology Control material because of elevated MCV results in specific lots.

    Product
    Boule Con-Diff Tri-Level Multi-Parameter Assayed Hematology Control, used for in vitro diagnostic use as a control to monitor the performance of multi-parameter hematology instruments.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1758-2014·2014-04-16

    Smiley National Recalls Kratom Products Due to Unapproved Ingredients

    Smiley National is voluntarily recalling four kratom products because they contain unapproved dietary ingredients.

    Product
    Natural Bali Kratom 40, capsule, UPC code 5410600335, 20 capsules per bottle.
    Category
    Food
    Distribution
    Distributed nationwide