The Recall Desk

State

Northern Mariana Islands product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44126–44150 of 73832

  • SevereFDA (Devices)·Z-1409-2017·2017-03-15

    FDA Recalls Premier Guard Drape Due to Sterility Compromise

    The FDA is recalling Premier Guard Drape, Sterile, because the sterile barrier was breached, compromising sterility. The product is used with RF Surgical Gauze detection systems.

    Product
    Premier Guard Drape, Sterile. For Use with Verisphere (01-0035) and ArQ.Sphere (01-0044) Item Number: 01-0037 Used in conjunction RF Surgical Gauze detection systems to protect scanning device from contamination during various surgical procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1428-2017·2017-03-15

    Villa Sistemi Medicali Recalls Apollo X-Ray Systems Due to Footrest Detachment

    Villa Sistemi Medicali is recalling 65 Apollo multi-function x-ray systems because the footrest detached from the table, causing a patient to fall.

    Product
    Apollo; Models: 9784000131 9784000231 9784020131 9784020231 9784100231 9784120131 9784120231 9784130131 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1408-2017·2017-03-15

    FDA Recalls Premier Guard Sterile Drapes Due to Sterility Compromise

    The FDA is recalling Premier Guard Sterile Drapes because the sterile barrier was breached, compromising sterility. The recall covers 1,111,600 units distributed nationwide.

    Product
    Premier Guard Sterile Drape For Use with Blair-Port Wand (02-0029) and Blair-Port Wand X (01-0046) Item Number: 01-0020 Used in conjunction RF Surgical Gauze detection systems to protect scanning device from contamination during various surgical procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0513-2017·2017-03-15

    McKesson Recalls Aspirin Chewable Tablets Due to Foreign Material

    McKesson Packaging Services is recalling 6,717 cartons of 81 mg Aspirin Chewable Tablets because foreign material was found in the bulk inventory.

    Product
    Aspirin Chewable Tablets, 81 mg, (NSAID*), packaged in UD 750 Tablets (25 x 30) tablets in blisters per carton, Dist. By: McKesson Packaging Services, a business unit of McKesson Corporation, 7101 Weddington Rd., Concord, NC 28027, NDC 63739-434-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1432-2017·2017-03-15

    Siemens PRIMUS HI and Mevatron M2 Linear Accelerators Recalled for Weld Defect

    Siemens is recalling 35 PRIMUS HI and Mevatron M2 linear accelerators due to a defective weld seam that could cause overhead suspensions to fall and injure people.

    Product
    PRIMUS HI and Mevatron M2/Primus Mid-Energy, Accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0492-2017·2017-03-15

    Mylan Recalls Mirtazapine Tablets Due to Foreign Glipizide Contamination

    Mylan Pharmaceuticals is recalling Mirtazapine tablets because bottles may contain foreign Glipizide 10 mg tablets. Consumers should stop using the product and contact their pharmacist.

    Product
    MIRTAZAPINE — MIRTAZAPINE (MIRTAZAPINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1433-2017·2017-03-15

    Siemens Medical Recalls 35 MEVATRON M 6700 Linear Accelerators

    Siemens Medical Solutions USA is recalling 35 MEVATRON M 6700 linear accelerators due to a defective weld seam that could cause the overhead suspension to fall and injure a patient or other person.

    Product
    MEVATRON M 6700 (MX) Accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1430-2017·2017-03-15

    Villa Sistemi Medicali Recalls Apollo EZ X-Ray Systems Due to Footrest Detachment

    Villa Sistemi Medicali is recalling 65 Apollo EZ x-ray systems because the footrest detached from the table, causing a patient to fall.

    Product
    Apollo EZ; Model: 9784152036 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1532-2017·2017-03-15

    Pharmanex ageLOC TR90 Protein Boost Recalled for Undeclared Milk Allergen

    Nu Skin is voluntarily recalling Pharmanex ageLOC TR90 Protein Boost because it contains an undeclared milk allergen.

    Product
    Pharmanex ageLOC TR90 Protein Boost. Protein Powder. Net wt. 1.59 lbs (720g). 30 Servings. Natural Vanilla Flavor. Lactose, Gluten, & Soy Free. Plant Protein/Vegetarian.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1429-2017·2017-03-15

    Apollo DRF X-ray Systems Recalled Due to Footrest Detachment Hazard

    Villa Sistemi Medicali is recalling 65 Apollo DRF x-ray systems because the footrest can detach, causing patients to fall from the table.

    Product
    Apollo DRF; Model: 9784220831 Product Usage: General, multi-function x-ray systems capable of routine radiographs and general fluoroscopy procedures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1437-2017·2017-03-15

    Siemens MEVATRON KD-2 Linear Accelerators Recalled for Defective Weld Seams

    Siemens is recalling 35 MEVATRON KD-2 linear accelerators due to defective weld seams that could break and cause the overhead suspension to fall, posing a risk of severe injury.

    Product
    MEVATRON KD-2, accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1436-2017·2017-03-15

    Siemens Medical Linear Accelerators Recalled for Defective Overhead Suspension Welds

    Siemens is recalling 35 linear accelerator systems due to defective weld seams that could cause overhead suspensions to fall, posing a risk of severe injury.

    Product
    MEVATRON MD-2, MEVATRON MDX-2 and MEVATRON ME, accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1585-2017·2017-03-15

    Versa Marketing Recalls Fusia Szechuan Stir Fry Due to Listeria

    Versa Marketing is recalling Fusia Asian Aspirations Szechuan Stir Fry because the product tested positive for Listeria monocytogenes. The recall affects 4,089 cases sold at Aldi stores nationwide.

    Product
    Fusia Asian Aspirations Szechuan Stir Fry; A delicious blend of premium vegetables with a savory sauce packed in a plastic bag: Sauce packet included. NET WT 21 oz. (1 lb 5 oz) 595 g
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1434-2017·2017-03-15

    Siemens Medical Linear Accelerators Recalled for Defective Weld Seams

    Siemens is recalling 35 MEVATRON M 6730/6740 linear accelerators because defective weld seams on overhead suspensions could break and fall, posing a risk of severe injury.

    Product
    MEVATRON M 6730/6740 (MEX) Accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1435-2017·2017-03-15

    Siemens MEVATRON M 7400/7440 Linear Accelerators Recalled for Defective Welds

    Siemens is recalling 35 MEVATRON M 7400/7440 linear accelerators because a defective weld seam could break, causing the overhead suspension to fall and potentially injure patients or others.

    Product
    MEVATRON M 7400/7440(MEX) Accelerator, Linear, Medical The intended use of the SIEMENS branded PRIMUS family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1576-2017·2017-03-15

    Stubb's Barbecue Sauce Recalled for Glass Bottle Defects

    McCormick & Co. is voluntarily recalling 18oz bottles of Stubb's Sticky Sweet BBQ Sauce due to glass defects that may cause chipped or missing glass.

    Product
    McCormick & Co., Inc., Stubbs Barbecue. 18oz Best By Date of January 17, 2020.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1420-2017·2017-03-15

    Siemens IMMULITE Progesterone Test Kits Recalled for DHEA-S Interference

    Siemens is recalling IMMULITE Progesterone test kits because DHEA-S causes falsely elevated results, potentially affecting diagnosis.

    Product
    IMMULITE/ IMMULITE 1000 Progesterone; Catalog Number: LKPW1; Siemens Material Number: 10381128 Product Usage: For in vitro diagnostic use with the IMMULITE¿2000 Systems Analyzers- for the quantitative measurement of progesterone in serum, as an aid in the diagnosis and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V182000·2017-03-15

    Ride The Ducks Recalls Amphibious Vehicles Due to Seat Belt Defect

    Ride The Ducks International LLC is recalling 1996-2014 amphibious vehicles because driver seats and seat belts may not secure occupants in a crash.

    Product
    RIDE THE DUCKS — RIDE THE DUCKS AMPHIBIOUS VEHICLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1399-2017·2017-03-15

    Parker Medical Recalls Left Double Lumen Endobronchial Tubes

    Parker Medical is recalling specific lots of Left Double Lumen Endobronchial Tubes because the single lung isolation feature did not function as intended.

    Product
    Parker Left Double Lumen Endobronchial Tube with Parker Flex-Tip (Parker Endo-Bronch with Flex Tip). Model Numbers: H-PFTDL-28-1, H-PFTDL-32-1, H-PFTDL-35-1, H-PFTDL-37-1, H-PFTDL-39-1, H-PFTDL-41-1. The product is an endotracheal tube with a double lumen for single lung…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1404-2017·2017-03-15

    See Clear Company Recalls Color Contact Lenses for Sterility and Labeling Issues

    The See Clear Company is recalling 119,829 units of color contact lenses because they may not be sterile and may have incorrect lot numbers or expiry dates.

    Product
    Color contact lenses labeled under the following brands: Diamond, Fierce, Ambition, Circle Collection, Lunatic, Fright, Desire and See Clear.
    Category
    Medical Device
    Distribution
    Distributed nationwide