The Recall Desk

State

Northern Mariana Islands product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52901–52925 of 73847

  • SevereCPSC·15182·2015-07-15

    Cooper Lighting Recalls Fluorescent Fixtures Due to Fire Hazard

    Cooper Lighting is recalling about 1.62 million fluorescent fixtures because the sockets can overheat, arc, and melt, posing a fire hazard.

    Product
    Cooper Lighting, Portfolio and Utilitech fluorescent lighting fixtures
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1950-2015·2015-07-15

    Shiley Neonatal and Pediatric Tracheostomy Tubes Recalled for Breathing Difficulties

    FDA is recalling Shiley Neonatal and Pediatric Tracheostomy Tubes because patients reported discomfort and breathing difficulties after switching to these products.

    Product
    Shiley Neonatal, Pediatric and Long Pediatric Tracheostomy Tube, Cuffless. Model Numbers…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1089-2015·2015-07-15

    Teva Recalls Adrucil Fluorouracil Injection Due to Particulate Matter

    Teva Pharmaceuticals is recalling Adrucil (fluorouracil injection) vials due to the presence of black particulate matter, including silicone rubber and drug crystals.

    Product
    Adrucil (fluorouracil injection, USP) Pharmacy Bulk Package Not for Direct Infusion, 5 g/100 mL (50 mg/mL), For Intravenous Use Only, Rx Only, Teva Parenteral Medicines, Inc., Irvine, CA 92618, NDC 0703-3019-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2425-2015·2015-07-15

    New Punjab Ladoo Recalled for Missing Ingredient Label and Undeclared Allergens

    New Punjab Sweets Inc. is voluntarily recalling Ladoo snacks because they lack an ingredient label and may contain undeclared nuts, colors, and wheat.

    Product
    New Punjab Ladoo is a ball-shaped Indian snack coated with almonds and/or pistachios. Product is packaged in clear plastic container with a clear plastic lid. Container sizes are 1lb. and 0.5lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2427-2015·2015-07-15

    New Punjab Rosgula Recalled for Undeclared Almonds, Colors, and Wheat

    New Punjab Sweets Inc. is voluntarily recalling Rosgula snacks due to undeclared almonds, colors, and wheat.

    Product
    New Punjab Rosgula is a ball-shaped Indian snack. Product is packaged in clear plastic container with a clear plastic lid. Container sizes are 1lb. and 0.5lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1990-2015·2015-07-15

    Maquet Surgical Light Suspension Arms Recalled for Debris Risk

    Maquet is recalling 646 PowerLED, X-TEN, and VOLISTA surgical light systems because suspension arms may grind and release paint chips into the surgical field.

    Product
    The PowerLED / X-TEN / VOLISTA Surgical Light Systems are surgical light systems intended to be used to provide visible illumination of the surgical area or the patient. Ceiling surgical light systems typically include one or more arms that are able to rotate 360 degrees around…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1987-2015·2015-07-15

    Philips GoSafe Communicator 7000L Personal Emergency Response System Recall

    Lifeline Systems is recalling 38 Philips GoSafe Communicator 7000L units because they may fail to sense the phone line under unusual landline conditions.

    Product
    Philips GoSafe Communicator 7000L Personal emergency response system.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2424-2015·2015-07-15

    New Punjab Kaju Fry Recalled for Undeclared Cashew Nuts

    New Punjab Sweets Inc. is voluntarily recalling Kaju Fry (toasted fried cashews) because the product may contain undeclared cashew nuts.

    Product
    New Punjab Kaju (Kajoo) Fry is the Indian translation for Toasted Fried Cashews. Product is packaged in clear plastic container with a clear plastic lid. Container sizes are 1lb. and 0.5lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·15185·2015-07-15

    Bexco Recalls DaVinci Cribs Due to Entrapment and Fall Hazards

    Bexco is recalling DaVinci brand cribs because a metal bracket can break, creating gaps that pose entrapment, fall, and laceration risks to infants.

    Product
    DaVinci Cribs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2421-2015·2015-07-15

    New Punjab Burfi Recalled for Undeclared Nuts

    New Punjab Sweets Inc. is voluntarily recalling New Punjab Burfi because the Indian snack may contain undeclared almonds, pistachios, and cashews.

    Product
    New Punjab Burfi is an Indian snack cut into 1lb or 0.5 lb. squares. Product is packaged in clear plastic container with a clear plastic lid.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2426-2015·2015-07-15

    New Punjab Chum Chum Recalled for Undeclared Allergens and Colors

    New Punjab Sweets Inc. is voluntarily recalling Chum Chum snacks due to undeclared almonds, coconut, wheat, and food colors.

    Product
    New Punjab Chum Chum is a oval-shaped Indian snack coated with almonds and/or coconuts. Product is packaged in clear plastic container with a clear plastic lid. Container sizes are 1lb. and 0.5lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1986-2015·2015-07-15

    BTE Technologies Recalls Primus Exercise Devices Due to Detachment Risk

    BTE Technologies is recalling 510 Primus rehabilitation devices because the optional Chop / Lift Bar may detach, posing a fall hazard to users.

    Product
    Primus (THE BTE WS30), model PrimusRS (PRRS) and Primus+ (PR30) a measuring exercise equipment device designed to provide active and passive torque resistance to patient motion during rehabilitation therapy. The Primus that includes the optional Chop / Lift Bar.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15186·2015-07-15

    Olympus Recalls VG 170 Digital Cameras Due to Electric Shock Hazard

    Olympus is recalling about 1,200 VG 170 digital cameras sold at HHGregg because an improperly installed part poses an electric shock risk. No injuries have been reported.

    Product
    Olympus VG 170 Digital Cameras
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2034-2015·2015-07-15

    Stradis Pediatric Pack Recalled Due to Medtronic Component Recall

    Stradis Healthcare is recalling Pediatric Packs containing Devon Light Gloves due to a manufacturer recall of the glove component by Medtronic.

    Product
    Pediatric Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1993-2015·2015-07-15

    Stradis Basic Pack Recalled Due to Medtronic Component Recall

    Stradis Healthcare is recalling Basic Packs containing Devon Light Gloves because the manufacturer, Medtronic, is recalling the glove component.

    Product
    Basic Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2423-2015·2015-07-15

    New Punjab Kaju Roll Recalled for Undeclared Cashews and Colors

    New Punjab Sweets Inc. is voluntarily recalling Kaju Roll snacks because they may contain undeclared cashews and artificial colors Yellow 5 and 6.

    Product
    New Punjab Kaju Roll is an Indian snack cut into squares. Product is packaged in clear plastic container with a clear plastic lid. Container sizes are 1lb. and 0.5lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2041-2015·2015-07-15

    Stradis Arthroscopy Packs Recalled Due to Component Recall

    Stradis Healthcare is recalling Arthroscopy Packs because they contain Devon Light Gloves, which are being recalled by the manufacturer Medtronic.

    Product
    Arthroscopy Pack - contains Devon Light Glove Used during surgery
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2422-2015·2015-07-15

    New Punjab Kaju Katri Recalled for Undeclared Cashews and Colors

    New Punjab Sweets Inc. is voluntarily recalling Kaju Katri Indian snacks because they may contain undeclared cashews and artificial colors Yellow 5 and 6.

    Product
    New Punjab Kaju Katri is an Indian snack cut into squares. Product is packaged in clear plastic container with a clear plastic lid. Container sizes are 1lb. and 0.5lbs.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·15V448000·2015-07-15

    Spartan Emergency Response Vehicles Recalled for Valve Stem Wear

    Spartan is recalling 2007-2015 emergency response vehicles because front wheel valve stems may rub against brake calipers, causing sudden tire deflation.

    Product
    SPARTAN — SPARTAN GLADIATOR, METROSTAR, ADVANTAGE, DIAMOND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2045-2015·2015-07-15

    Volcano ComboMap Intravascular System Recalled for Interoperability Limitation

    Volcano Corp is recalling 227 ComboMap Intravascular Flow and Pressure Systems due to a limitation in interoperability with the Philips Xper Flex Cardia Physiomonitoring System.

    Product
    ComboMap Intravascular Flow and Pressure System; Product/Part number: Combo Map - 802745-001. Intravascular Imaging and Pressure System for evaluation of blood flow, perfusion and vascular structures.
    Category
    Medical Device
    Distribution
    Distributed nationwide