The Recall Desk

State

Northern Mariana Islands product recalls

73,576 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 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27276–27300 of 73599

  • HighNHTSA·20V655000·2020-10-26

    2021 Forest River Cardinal Fifth-Wheel Trailers: Furnace Exhaust Intrusion Risk

    Forest River is recalling 2021 Cardinal fifth-wheel trailers. The furnace intake sleeve is too short and does not properly connect to the exterior, allowing furnace exhaust to enter the trailer and cause carbon monoxide poisoning.

    Product
    FOREST RIVER — FOREST RIVER CARDINAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V656000·2020-10-26

    2019-2021 Forest River Palomino Trailers Antenna Detachment Safety Recall

    Forest River is recalling 2019-2021 Palomino trailers because the antenna wing may not be properly secured, allowing it to detach while moving and create a road hazard.

    Product
    FOREST RIVER — FOREST RIVER PALOMINO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V654000·2020-10-26

    Forest River Cherokee recreational trailers recalled for electrical fire risk

    Forest River is recalling 2019-2021 Cherokee recreational trailers due to inadequate wiring insulation on shore cord inlets, which can increase fire risk. Owners should contact Forest River for recall details.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V651000·2020-10-23

    Mercedes-Benz Recalls 2020 GLC Models for Steering Wiring Defect

    Mercedes-Benz is recalling 2,533 2020 GLC models because a damaged steering wiring harness could cause loss of power assist or a fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 300, AMG GLC63, AMG GLC43, GLC 350 E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V650000·2020-10-22

    GM Recalls 2019-2020 Silverado and Sierra Trucks for Driveshaft Defect

    General Motors is recalling 2019-2020 Chevrolet Silverado and GMC Sierra trucks because a driveshaft joint may not be properly welded, risking separation and loss of propulsion.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 2500, SILVERADO 1500, SIERRA 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21704·2020-10-22

    Rocky Mountain Oils Recalls Wintergreen Essential Oil and Blends for Packaging Defect

    Rocky Mountain Oils is recalling Wintergreen essential oil and four oil blends because the packaging is not child-resistant, posing a risk of poisoning to young children.

    Product
    Wintergreen essential oil, and Pain Ease, Sports Pro, True Blue, Relieve Me oil blends
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0016-2021·2020-10-21

    Seneca Cinnamon Apple Crisps Recalled for Salmonella Contamination

    Seneca Foods is recalling Cinnamon Apple Crisps due to potential Salmonella contamination. The recall covers specific brands and sizes distributed nationwide.

    Product
    Cinnamon Apple Crisps packaged under the following Brands and sizes: 1. Seneca, 2.5 ounce, UPC 0 18195-70100 8; 2. Clancy's 2.5 ounce, UPC 41498-27266. 3. Seneca, 0.7 ounce, UPC 0 18195-70140 4 4. Seneca 20 lb. 1" dices, product code 10134
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0096-2021·2020-10-21

    Handicare SwiftHook Component Recall for Mobile and Ceiling Lifts

    Handicare AB is recalling SwiftHook components used in mobile and ceiling lifts because the carry bar may detach during use, posing a risk of injury to patients and caregivers.

    Product
    SwiftHook sold as the following: a. Individually as SwiftHook b. Included with Vega505EE mobile lifts Product Usage: The mobile lifts are intended to assist people with functional impairments in scenarios involving physical positioning.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0022-2021·2020-10-21

    Lucky Spoon Bakery Recalls Gluten-Free Zucchini Cupcakes Due to Gluten Contamination

    Lucky Spoon Bakery is recalling gluten-free zucchini cupcakes because a flour batch tested positive for gluten. The products were distributed in eight states and nationwide via drop ship.

    Product
    Lucky Spoon Bakery Gluten Free Frosty Zucchini Cupcakes, 8.0 oz. plastic clam shell containing 4 cupcakes, UPC 8-50489-00311-1, P.O. Box 2954 Salt Lake City, UT 84110. 12 packages/case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0025-2021·2020-10-21

    Lucky Spoon Bakery Recalls Gluten-Free Chocolate Cake Due to Gluten Contamination

    Lucky Spoon Bakery is recalling its Gluten Free Chocolate Celebration Cake because a batch of flour used in production tested positive for gluten.

    Product
    Lucky Spoon Bakery Gluten Free Chocolate Celebration Cake, 17.5 oz. plastic clam shell containing 1 cake, UPC 8-50489-00322-7, P.O. Box 2954 Salt Lake City, UT 84110. 6 packages/case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0021-2021·2020-10-21

    Lucky Spoon Bakery Recalls Gluten-Free Chocolate Cupcakes Due to Gluten Contamination

    Lucky Spoon Bakery is recalling gluten-free chocolate cupcakes because a flour supplier batch tested positive for gluten. The products were distributed in eight states and nationwide via drop ship.

    Product
    Lucky Spoon Bakery Gluten Free Chocolate Cupcakes with Vanilla Buttercream Frosting, 8.0 oz. plastic clam shell containing 4 cupcakes, UPC 8-50489-00310-4, P.O. Box 2954 Salt Lake City, UT 84110. 12 packages/case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·21010·2020-10-21

    Jakks Pacific Recalls MorfBoard Skate Scooters Due to Fall Hazard

    Jakks Pacific is recalling MorfBoard Skate & Scoot Combo scooters with "Y" handlebars because the joint can break, posing a fall hazard.

    Product
    MorfBoard Skate & Scoot Combo scooters with "Y" handlebars
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0024-2021·2020-10-21

    Lucky Spoon Bakery Recalls Gluten-Free Pumpkin Cupcakes Due to Gluten Contamination

    Lucky Spoon Bakery is recalling gluten-free pumpkin cupcakes because a flour batch tested positive for gluten. The products were distributed in eight states and nationwide via drop ship.

    Product
    Lucky Spoon Bakery Gluten Free Fall Frost Pumpkin Cupcake, 8.0 oz. plastic clam shell containing 4 cupcakes, UPC 8-50489-00320-3, P.O. Box 2954 Salt Lake City, UT 84110. 12 packages/case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·21011·2020-10-21

    CB2 Recalls Trace Bookcases Due to Risk of Collapse and Injury

    CB2 is recalling Trace bookcases because the frame can collapse when fully loaded, posing an injury hazard. Consumers should stop using the units and contact CB2 for a replacement or refund.

    Product
    Trace bookcases
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0094-2021·2020-10-21

    Genicon Aquas PowerFlow Tube Set Recalled for Lack of FDA Clearance

    Genicon, Inc. is recalling 10,808 units of the Aquas PowerFlow Tube Set because the device design did not receive proper premarket clearance from the FDA.

    Product
    Aquas PowerFlow Tube Set - Product Usage: The device delivers sterile irrigation fluids to surgical sites during laparoscopic procedures and to evacuate blood, tissue debris, and smoke from the surgical site
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0091-2021·2020-10-21

    Mizuho OSI Recalls Levo Arms Due to Fluid Ingress Risk

    Mizuho OSI is recalling 174 Levo Arms used in spinal surgery tables due to a potential fluid ingress issue that could cause the locking mechanism to fail.

    Product
    Levo Arm Label: LEVO ARM REF 7887-050 MIZUHO OSI Refurbished Levo Arm Label: LEVO ARM REF 7887-050R MIZUHO OSI - Product Usage: used with Mizuho OSI spinal surgery tables to provide patient head support and positioning during spinal surgery.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0109-2021·2020-10-21

    SkyVision SDS System Recalled for Intermittent Video Signal Failure

    Skytron is recalling 36 SkyVision SDS System units because intermittent signal failures can cause monitors to go blank during surgery, increasing patient risk.

    Product
    SkyVision SDS System - Video Integration Model: GC-SDS-BSCB-200 - Product Usage: is a high quality, self-contained video switching and control unit for use in the operating room.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0023-2021·2020-10-21

    Lucky Spoon Bakery Recalls Gluten-Free Brownie Bites Due to Gluten Contamination

    Lucky Spoon Bakery is recalling specific lots of Gluten Free Chewy Chocolatey Brownie Bites because a flour supplier's batch tested positive for gluten.

    Product
    Lucky Spoon Bakery Gluten Free Chewy Chocolatey Brownie Bites, 6.6 oz. plastic clam shell containing approximately 12 (6.6 oz.), UPC 8-50489-00315-9, P.O. Box 2954 Salt Lake City, UT 84110. 12 packages/case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0020-2021·2020-10-21

    Lucky Spoon Bakery Recalls Gluten-Free Cupcakes Due to Gluten Contamination

    Lucky Spoon Bakery is recalling gluten-free cupcakes because a flour batch tested positive for gluten. The products were distributed in eight states and nationwide via drop ship.

    Product
    Lucky Spoon Bakery Gluten Free Very Vanilla Cupcakes with Vanilla Buttercream Frosting, 8.0 oz. plastic clam shell containing 4 cupcakes, UPC 8-50489-00309-8, P.O. Box 2954 Salt Lake City, UT 84110. 12 packages/case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0019-2021·2020-10-21

    Lucky Spoon Bakery Recalls Gluten-Free Muffins Due to Gluten Contamination

    Lucky Spoon Bakery is recalling Gluten Free Utterly Almond Muffins because a flour supplier's batch tested positive for gluten.

    Product
    Lucky Spoon Bakery Gluten Free Utterly Almond Muffins, 7.25 oz. plastic clam shell containing 6 muffins, UPC 8-50489-00305-0, P.O. Box 2954, Salt Lake City, UT 84110. 12 packages/case
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·20V647000·2020-10-21

    Braun Ambulances Recall 156 Units Due to Display Lockup

    Braun Ambulances is recalling 156 units because the lighting and HVAC display may lock up, potentially delaying emergency operations and increasing crash risk.

    Product
    BRAUN AMBULANCES — BRAUN AMBULANCES EXPRESS PLUS TYPE I, CHIEF XL TYPE III, LIBERTY TYPE I, EXPRESS TYPE III
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0095-2021·2020-10-21

    Alcon Custom-Pak Surgical Packs Recalled for Latex Glove Degradation

    Alcon is recalling 16,971 Custom-Pak Surgical Procedure Packs containing Cardinal Health PROTEXIS Latex Micro Surgical Gloves due to a degradation defect that could cause holes or tears.

    Product
    Alcon Custom-Pak Surgical Procedure Packs containing Cardinal Health" PROTEXIS" Latex Micro Surgical Gloves - Product Usage: used by ophthalmic surgeons in a variety of ophthalmic surgeries.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0097-2021·2020-10-21

    Biomet Recalls RingLoc Hip Cups Due to Double Sterilization

    Biomet is recalling 48 RingLoc Bi-Polar Hip System Acetabular Cups because they were gamma sterilized twice, which may compromise functionality and shelf life.

    Product
    (1) RingLoc Bi-Polar Hip System Acetabular Cup ArCom: Acetabular Bi-Polar Cup, E1 Antioxidant Infused, 28 MM, 41 MM: Item No. 110010458; Lot No. 710930; UDI No. (01) 00880304568747 (17) 230614 (10) 710930 (2) RingLoc Hip system Acetabular Bi-Polar Cup: Acetabular Cup…
    Category
    Medical Device
    Distribution
    Distributed nationwide