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.

54651–54675 of 73850

  • SevereFDA (Food)·F-1803-2015·2015-04-08

    My Spice Sage Ground Cumin Recalled for Undeclared Peanut

    Zenobia Company LLC is recalling My Spice Sage Ground Cumin because it may contain undeclared peanut protein. The recall covers 1,467 units sold nationwide.

    Product
    My Spice Sage CUMIN GROUND under the following labels and packaging: 1) NET WT 1 oz (28g) UPC 00105001, packed in a plastic resealable bag 2) NET WT 4 oz (113g) UPC 00105004 packed in a plastic resealable bag, 3) NET WT 4.9 oz (139g) UPC 00105000 packed in a plastic bottle, 4)…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1872-2015·2015-04-08

    Healthy Mama Boost It Up Protein Drink Recalled for Undeclared Milk

    Maternal Science Inc. is recalling Healthy Mama Boost It Up Mango with Ginger Protein Drink because it contains undeclared milk.

    Product
    Healthy Mama Boost it Up Mango with Ginger Caffeine Free Protein with Energy Drink 12 fl oz Distributed by: Maternal Science, Inc. 50 Tice Boulevard, Suite 340 Woodcliff Lake, NJ 07677 UPC 810758020058
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V210000·2015-04-08

    KTM Recalls 2015 690 Enduro R Motorcycles Due to Rear Brake Line Damage

    KTM is recalling 409 model year 2015 690 Enduro R motorcycles because the rear brake line may be damaged, potentially causing a loss of braking ability and increasing crash risk.

    Product
    KTM — KTM 690 ENDURO R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1790-2015·2015-04-08

    Archer Farms Ground Cumin Recalled for Undeclared Peanut Allergen

    Brinkhoff & Monoson Inc is recalling Archer Farms ground cumin because it may contain undeclared peanut allergens.

    Product
    Archer Farms Cumin, ground, packaged in 6 oz clear square glass bottle with a silver metal cap and a label weight of 2.8oz (79 g), Distributed by Target Corp. Minneapolis, MN;
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1789-2015·2015-04-08

    Brinkhoff & Monoson Dark Chili Powder Recalled for Undeclared Peanut Allergen

    Brinkhoff & Monoson is recalling Dark Chili Powder distributed by The Fresh Market because it contains cumin that may be contaminated with undeclared peanut allergens.

    Product
    Dark Chili Powder packaged in the following configurations: (1) a 5 by 7 in clear square bag with a zipper seal and a label weight of 2.24 oz (63.5 g), Distributed by The Fresh Market, Greensboro, NC, and (2) 4 oz clear square glass bottle with a silver metal cap and a label…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1806-2015·2015-04-08

    Gilster-Mary Lee Recalls Honey & Oat Mixers Cereal for Undeclared Almonds

    Gilster-Mary Lee Corp. is recalling Honey & Oat Mixers dry cereal because it contains undeclared almonds, a major food allergen.

    Product
    Honey & Oat Mixers ready-to-eat dry cereal sold under the market pantry brand and packaged in card stock cartons with a new weight of 18 oz. (1 lb. 2 oz.) 510 g.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1357-2015·2015-04-08

    DePuy RECLAIM Hip Implant Inserter Adaptor Recalled for Fracture Risk

    DePuy Orthopaedics is recalling 54 units of the RECLAIM Assembled Implant Inserter Adaptor because the instrument may fracture during surgery, potentially leaving plastic pieces in the patient.

    Product
    RECLAIM Assembled Implant Inserter Adaptor orthopedic manual surgical instrument for hip implantation.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1873-2015·2015-04-08

    Healthy Mama Protein Drink Recalled for Undeclared Milk Allergen

    Maternal Science Inc. is recalling 60 units of Healthy Mama Boost it Up Pom Cherry Caffeine Free Protein with Energy Drink because it contains undeclared milk.

    Product
    Healthy Mama Boost it Up Pom Cherry Caffeine Free Protein with Energy Drink 12 fl oz Distributed by: Maternal Science, Inc. 50 Tice Boulevard, Suite 340 Woodcliff Lake, NJ 07677 UPC 810758020126
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1788-2015·2015-04-08

    See's Candies Recalls Classic Red Hearts for Missing Tree Nut Labeling

    See's Candies is recalling 8 oz. Classic Red Hearts with Assorted Chocolates because the packaging failed to list tree nuts in the ingredient statement.

    Product
    See's Candies Classic Red Heart with Assorted Chocolates (8 oz. 227 g), 42 hearts per carton; UPC 737666091201 Ingredients: Sugar, Cream, Chocolate , Cocoa Butter, Corn Syrup, milk, brown sugar, butter, honey, egg whites, molasses, salt, gelatin, vanilla, baking soda…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1364-2015·2015-04-08

    Biomet Recalls Ziploop Button and ToggleLocs Due to Packaging Seal Issues

    Biomet, Inc. is recalling 50 units of Ziploop Buttons and ToggleLocs manufactured in 2014 because sterile packaging was not properly sealed.

    Product
    Ziploop Button Product Usage: The Ziploop Button is a non-resorbable system intended to aid in ACL reconstructive procedure due to injury or degenerative disease
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1875-2015·2015-04-08

    Michael Foods Recalls Frozen Egg Patties Due to Undeclared Milk Allergen

    Michael Foods is recalling 181,127 cases of frozen egg patties because they contain milk, an allergen not declared on the label.

    Product
    Natural Shaped Fried Egg (patties), 1.75 oz. frozen egg patties, packaged 144-count per case, Net WT. 15.75 lb. (7.14 KG), under two brand names: (1) Pappetti's Table Ready, UPC Code 46025 85879. The responsible firm name on the label is Michael Foods Inc., Minnetonka, MN…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1341-2015·2015-04-08

    Microtek Medical Recalls Laparoscopic Tubing Sets Due to Unlabeled Latex Packaging

    Microtek Medical Inc. is recalling 270 units of sterile laparoscopic tubing sets because the packaging contains latex but lacks the required warning label.

    Product
    LAPAROSCOPIC TUBING SET, 3/16" ¿ X 10' (48cm x 304.8cm) WITH MALE LUER LOCK - STERILE, REF 24311 QTY 10/CS, STERILE EO Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1371-2015·2015-04-08

    Edwards Lifesciences Recalls Fem-Flex II Pediatric Femoral Arterial Cannulas

    Edwards Lifesciences is recalling specific sizes of the Fem-Flex II Pediatric Femoral Arterial Cannula due to a protruding wire at the tip that could cause tissue damage.

    Product
    Edwards Lifesciences Fem-Flex II Femoral Arterial Cannula 8, 10, 12 French,Sterile EO, Rx Only, Manufacturer Edwards Lifesciences LLC, Irvine, CA.-Model Numbers: FEMII008A, FEMII008AT, FEMII008V, FEMII010A, FEMII010AT, FEMII010V, FEMII012A, FEMII012AT, and FEMII012V. Edwards…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15726·2015-04-08

    Dimension Industries Recalls Patio Set Rockers Due to Fall Hazard

    Dimension Industries is recalling Hampton Bay-branded patio set rockers sold at Home Depot because the chairs can break during normal use, posing a fall hazard.

    Product
    Patio set rockers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1338-2015·2015-04-08

    Microtek Medical Recalls Surgical Helmet Motor Modules for Latex Packaging

    Microtek Medical Inc is recalling 38 units of FREEDOMAIRE Motor Modules because the packaging contains latex but lacks the required warning label.

    Product
    FREEDOMAIRE(R) MOTOR MODULE, REF 11112STK, QTY 1/CS, NON STERILE, NO LATEX The Surgical Helmet System is intended to be worn by surgical personnel to provide barrier between the operating environment and the surgical personnel in order to protect against contamination, body…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1346-2015·2015-04-08

    Microtek Medical Smoke Evacuator Tubing Set Recalled for Latex Packaging

    Microtek Medical is recalling smoke evacuator tubing sets because the packaging contains latex but lacks the required warning label.

    Product
    TUBING SET 7/8" X 6' WITH 1/4" x 24" TUBING, REF 24136, QTY 3/CS, NON STERILE, NO LATEX Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures. Locations include…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1363-2015·2015-04-08

    Biomet Recalls ToggleLoc and Ziploop Fixation Devices Due to Packaging Defects

    Biomet is recalling ToggleLoc and Ziploop devices manufactured in 2014 because sterile packaging was not sealed, potentially compromising sterility.

    Product
    ToggleLoc; fastener, fixation, non degradable, soft tissue; Artificial Ligament Fixation Device #7 PE Ziploop Extended Toggleloc Product Usage: The Toggleloc System is a non-resorbable system intended to aid in arthroscopic and orthopedic reconstructive procedures requiring…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1674-2015·2015-04-08

    Health One Pharmaceuticals Recalls Salvia Dietary Supplements

    Health One Pharmaceuticals is recalling Salvia dietary supplements due to significant violations of current good manufacturing practices (cGMP) regulations.

    Product
    Salvia, 100 Vegetarian Capsules, 500mg
    Category
    Food
    Distribution
    Distributed nationwide