The Recall Desk

State

Northern Mariana Islands product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35451–35475 of 73760

  • SevereNHTSA·19V049000·2019-01-23

    Spartan K1 Motor Home Chassis Recalled for Brake Component Defect

    Spartan is recalling 2019-2020 K1 motor home chassis because missing or improper cotter pins may cause brake actuator rods to detach, increasing stopping distance.

    Product
    SPARTAN — SPARTAN K1
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0724-2019·2019-01-23

    Arthrex Suture Anchor Recall Due to Potential Breakage During Insertion

    Arthrex is recalling Nano Corkscrew FT Suture Anchors because they may break during insertion. The recall covers 1,418 units distributed in the US and abroad.

    Product
    Arthrex Suture Anchor, Nano Corkscrew FT (consists of an anchor pre-loaded on a handled inserter including suture, with needles.) Part Number AR-1317FT Product Usage: Soft tissue fixation to bone in the hand and wrist
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0750-2019·2019-01-23

    Kimberly-Clark Recalls U by Kotex Sleek Tampons for Structural Defect

    Kimberly-Clark is recalling U by Kotex Sleek tampons because they may come apart upon removal. The recall covers 68,852,076 units distributed nationwide and in Canada.

    Product
    U by Kotex¿ Sleek¿, Regular/Super Tampons, 34 Count Multipack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0735-2019·2019-01-23

    Zimmer Biomet Recalls Maximum Variable Pitch Compression Screw Caddy

    Zimmer Biomet is recalling 971 Maximum Variable Pitch Compression Screw Caddies due to a potential for silicone shedding during cleaning and sterilization.

    Product
    Maximum Variable Pitch Compression Screw Caddy, Reference Number 231201003 Product Usage: Intended to carry implants and instruments during regular inventory distribution and handling and sterilization in the hospitals
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0749-2019·2019-01-23

    U by Kotex Sleek Regular Tampons Recalled for Potential Breakage

    Kimberly-Clark is recalling U by Kotex Sleek Regular Tampons because they may come apart upon removal.

    Product
    U by Kotex¿ Sleek¿, Regular Tampons, 34 Count
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0734-2019·2019-01-23

    Zimmer Biomet Recalls Compression Tray Bases Due to Silicone Shedding

    Zimmer Biomet is recalling 971 Maximum Variable Pitch Compression Tray Bases because they may shed silicone during cleaning and sterilization.

    Product
    Maximum Variable Pitch Compression Tray Base, Reference Number 231201002 Product Usage: Intended to carry implants and instruments during regular inventory distribution and handling and sterilization in the hospitals
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0732-2019·2019-01-23

    Meridian Premier Cryptococcal Antigen Test Recalled for Stability Issues

    Meridian Bioscience is recalling Premier Cryptococcal Antigen kits because an enzyme reagent may not maintain stability, potentially causing false negative results.

    Product
    PREMIER Cryptococcal Antigen, Catalog Number 602096 Product Usage: The PREMIER Cryptococcal Antigen enzyme immunoassay (EIA) is a screening or a semi-quantitative test system for the detection of capsular polysaccharide antigens of Cryptococcus neoformans in serum and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0733-2019·2019-01-23

    Waldemar Link LINK STEM Reconstruction Prosthesis Recalled for Depth Defect

    Waldemar Link is recalling 11 LINK STEM Reconstruction Prostheses because a manufacturing defect prevents the reaming guide from reaching the intended depth, which may lead to incorrect surgical positioning.

    Product
    LINK STEM with Microporous Surface MP Reconstruction Prosthesis, CEMENTLESS (Size XS-0, D: 12mm, L: 160mm), Reference Number 172-916/12 Product Usage: The LINK¿ STEM with Microporous Surface MP¿ Reconstruction Prosthesis, CEMENTLESS System is indicated for patients with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0745-2019·2019-01-23

    Bayer Medical Care Recalls MAVIG Portegra Overhead Counterpoise Systems

    Bayer Medical Care is recalling MAVIG Portegra and Portegra2 Overhead Counterpoise Systems because the head mount knob may not be properly tightened, causing the injector head to become loose or fall.

    Product
    MAVIG Portegra or Portegra2 Overhead Counterpoise System (OCS) used in conjunction with the Medrad Stellant CT Injection System (Certegra Workstation), Medrad Mark 7 Arterion" Injection System, or Medrad Mark V ProVis Injection System, Catalog Numbers: Catalog numbers: OCS CEIL…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0381-2019·2019-01-23

    Teva Recalls Olmesartan Medoxomil and Hydrochlorothiazide Tablets for Dissolution Failure

    Teva Pharmaceuticals USA is recalling specific lots of Olmesartan Medoxomil and Hydrochlorothiazide Tablets because they failed to meet dissolution specifications.

    Product
    Olmesartan Medoxomil and Hydrochlorothiazide Tablets, 40 mg/25 mg, packaged in a) 30-count bottle (NDC 0093-7617-56), b) 90-count bottle (NDC 0093-7617-98), Rx only, Manufactured In Israel By: Teva Pharmaceutical, IND. LTD., Jerusalem, 9777402, Israel, Manufactured For: Teva…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0723-2019·2019-01-23

    Arrow Pediatric Central Venous Catheter Recalled for Incorrect Labeling

    Arrow International Inc. is recalling specific lots of pediatric central venous catheters because the lidstock labels list incorrect priming volumes and flow rates.

    Product
    Arrow CVC 2 Lumen, Pediatric Two-Lumen Central Venous Cauterization Set with Blue FlexTip Catheter, 4 Fr 2 Lumen 5cm, Reference # CS-12402 The Arrow CVC is intended to provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0371-2019·2019-01-23

    Recall of Curaplex Epi Safe Kits Due to Expired Epinephrine Vials

    Bound Tree Medical is recalling 84 Curaplex Epi Safe Administration and Training Kits because the epinephrine vials inside expired in December 2018, despite the outer label showing January 2020.

    Product
    curaplex Epi Safe Administration and Training Kits # 8600-01100. Kit contains 2 Epi Safe Administration Kit (8600-01101) and 1 Epi Safe Training Kit (8600-01102), Rx Only. Distributed by Sarnova HC, LLC's family of companies: Bound Tree Medical, LLC, Cardio Partners, Inc.…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0379-2019·2019-01-23

    Bound Tree Medical Recalls Curaplex Epi Safe Kits Due to Labeling Errors

    Bound Tree Medical is recalling 747 Curaplex Epi Safe Kits because they are incorrectly labeled with an expiration date of May 2018 instead of May 2019, and the syringe component lacks 510(k) clearance.

    Product
    Curaplex Epi Safe Kit, Rx Only, contains: 1mL Vial of Epinephrine, 1 Epi-Safe Syringe, 1 Safety needle, 2 Alcohol Prep Pads,1 Adhesive Dressing, 1 Insert. Distributed by Sarnova, HC. LLC's family companies: Bound Tree Medical. LLC, Cardio Partners, Inc., Emergency Medical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V048000·2019-01-22

    Forest River Recalls 2017-2019 Motorhomes Due to Fire Risk

    Forest River is recalling 2017-2019 Glaval Entourage and Berkshire Coach Ultra motorhomes because a block heater cable defect may cause a fire.

    Product
    GLAVAL BUS — GLAVAL BUS, FOREST RIVER ENTOURAGE, BERKSHIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V047000·2019-01-21

    Mack Trucks Recalls 2018 Anthem and Pinnacle Models for Clutch Defect

    Mack Trucks is recalling 2018 Anthem and Pinnacle vehicles because a clutch component may fail, causing unintended movement and increasing crash risk.

    Product
    MACK — MACK PINNACLE (CXU), ANTHEM (AN)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·003-2019·2019-01-18

    Johnsonville Recalls Raw Pork Patties Due to Black Rubber Contamination

    Johnsonville is recalling raw ground pork patties potentially contaminated with black rubber. Consumers should discard or return the affected products.

    Product
    Johnsonville, LLC — Johnsonville, LLC Recalls Raw Ground Frozen Cheddar Cheese and Bacon Flavored Pork Patty Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V044000·2019-01-18

    Hino Recalls NJ8J Trucks for Missing Front Brake Dust Shields

    Hino is recalling 2007-2019 NJ8J trucks because missing front brake dust shields can cause the vehicle to pull left in wet conditions, increasing crash risk.

    Product
    HINO — HINO NJ8J
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V043000·2019-01-18

    Heartland Recalls 2019 Trailers Due to Incorrect Tire Certification Labels

    Heartland is recalling 2019 Prowler and Trail Runner trailers because their Federal Certification Labels may list incorrect tire size, load range, and pressure information.

    Product
    HEARTLAND — HEARTLAND TRAIL RUNNER, PROWLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V040000·2019-01-17

    Land Rover Recalls 2019 Models for Crankshaft Bolt Fracture Risk

    Jaguar Land Rover is recalling 2019 Range Rover and Discovery models because a crankshaft pulley bolt may fracture, causing engine failure and increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER VELAR, RANGE ROVER, RANGE ROVER SPORT, DISCOVERY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·002-2019·2019-01-17

    Perdue Recalls Gluten-Free Chicken Nuggets Due to Wood Contamination

    Perdue Foods is recalling approximately 68,244 pounds of SimplySmart Organics Gluten Free Chicken Nuggets due to possible wood contamination. Consumers should discard or return the product.

    Product
    Perdue Foods LLC — Perdue Foods LLC Recalls Simplysmart Organics Gluten Free Chicken Nugget Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide