The Recall Desk

State

Northern Mariana Islands product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32776–32800 of 73745

  • SevereFDA (Drugs)·D-1517-2019·2019-07-31

    Tris Pharma Recalls Hydrocodone and Chlorpheniramine Suspension Due to Potency Issues

    Tris Pharma is recalling 2,550 bottles of Hydrocodone Polistirex and Chlorpheniramine Polistirex Extended-Release Suspension due to high out-of-specification results for active ingredients and preservatives.

    Product
    HYDROCODONE POLISTIREX AND CHLORPHENIRAMINE POLISTIREX — HYDROCODONE POLISTIREX AND CHLORPHENIRAMINE POLISTIREX (HYDROCODONE POLISTIREX AND CHLORPHENIRAMINE POLISTIREX)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1522-2019·2019-07-31

    Geritrex Recalls Gericare Diocto Liquid Stool Softener Due to Microbial Contamination Risk

    Geritrex, LLC is recalling 6,165 bottles of Gericare Diocto Liquid Stool Softener due to cGMP deviations that may result in microbial contamination.

    Product
    Gericare Diocto Liquid Docusate Sodium Stool Softener, 50 mg/5mL, 16 FL OZ (473 ml), Dist. BY: Gericare Pharmaceuticals corp. 1650 63rd Street Brooklyn, NY 11204, NDC 57896-403-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1967-2019·2019-07-31

    PROBAR Meal Wholeberry Blast bars recalled for potential undeclared milk and soy allergens

    The FDA is recalling PROBAR Meal Wholeberry Blast bars because they may contain undeclared milk and soy ingredients. Consumers should discard affected bars and consult their healthcare provider if allergic.

    Product
    PROBAR MEAL Wholeberry Blast, Net Wt. 3oz.(85g), Film wrapped bar
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1525-2019·2019-07-31

    Geritrex Recalls Ritussin DM Due to Potential Microbial Contamination

    Geritrex, LLC is recalling Ritussin DM Double Strength cough syrup due to cGMP deviations that may result in microbial contamination.

    Product
    Ritussin DM Double Strength, 4 FL. OZ. (118 mL), RIJ Pharmaceutical Corporation 40 Commercial Avenue Middletown, NY 10941
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V563000·2019-07-31

    BMW Recalls 2018-2019 X3 and X4 Models for Seatback Welding Defect

    BMW is recalling 2018-2019 X3 and 2019 X4 vehicles because improperly welded front seatback frames may fold unexpectedly, increasing injury risk in a crash.

    Product
    BMW — BMW X3, X4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1524-2019·2019-07-31

    Geritrex Recalls Iron Elixir Due to Potential Microbial Contamination

    Geritrex, LLC is recalling Preferred Plus Pharmacy Iron Elixir due to cGMP deviations that may result in microbial contamination.

    Product
    Preferred Plus Pharmacy Iron Elixir Ferrous Sulfate, 220 mg, 16 fl oz. (473 mL), Distributed by: Geri-care Pharmaceuticals Corp. 1650 63rd Street Brooklyn, NY 11204, NDC 52807-177-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1521-2019·2019-07-31

    Geritrex Recalls Ritussin DM Due to Potential Microbial Contamination

    Geritrex, LLC is recalling 5,107 bottles of Ritussin DM Children & Adults due to cGMP deviations that may result in microbial contamination.

    Product
    Ritussin DM Children & Adults, 4 Fl. Oz. (118 mL), RIJ Pharmaceutical Corporation 40 Commercial Avenue Middletown, NY 10941, NDC 53807-409-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1527-2019·2019-07-31

    Geritrex Recalls Preferred Plus Dioctyl Liquid Stool Softener Due to Microbial Contamination

    Geritrex, LLC is recalling Preferred Plus Dioctyl Liquid Stool Softener due to cGMP deviations that may result in microbial contamination.

    Product
    Preferred Plus Dioctyl Liquid Stool Softener (Docusate Sodium), 50mg/5mL, 16 FL. Oz. (1 PT.) 473 mL, Manufactured by RIJ Pharmaceutical Corp. 40 Commercial Avenue Middletown, NY 10941, Distributed by Kinray Inc. Whitestone, NY 11357, NDC 53807-216-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1498-2019·2019-07-31

    Pharma-Natural Recalls Double Tussin DM Due to Manufacturing Violations

    Pharma-Natural Inc. is recalling 500 bottles of Double Tussin DM because the product was manufactured with current good manufacturing practice violations.

    Product
    DOUBLE TUSSIN DM (Dextromethorphan Hbr 20 mg, Guaifenesin 300 mg) in each 5ml teaspoon, 4 FL OZ (120 mL) bottle, Distributed by: Pamby Dist., Miami, FL 33414, NDC 63708-121-04.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1526-2019·2019-07-31

    Gericare Geri-Tussin DM Recalled for Potential Microbial Contamination

    Geritrex, LLC is recalling Gericare Geri-Tussin DM due to cGMP deviations that may result in microbial contamination.

    Product
    Gericare Geri-Tussin DM, 16 FL OZ (473 mL), Geri-care Phamaceuticals Corp. 1650 63rd Street Brooklyn, NY, NDC 57896-660-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1520-2019·2019-07-31

    Geritrex Recalls Diphenhydramine Oral Liquid Due to Potential Microbial Contamination

    Geritrex, LLC is recalling 8,645 bottles of Diphenhydramine Oral Liquid due to cGMP deviations that may result in microbial contamination.

    Product
    Diphenhydramine Oral Liquid Alcohol Free, 12.5 mg/5 mL, 4 fl oz (118 mL), RIJ Pharmaceutical Corporation 40 Commercial Avenue Middletown, NY 10941, NDC 53807-204-04
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1965-2019·2019-07-31

    Probar Meal Superfood Slam Bars Recalled for Undeclared Milk and Soy

    Probar LLC is recalling 2,908 Superfood Slam meal bars nationwide and in Canada due to undeclared milk and soy allergens.

    Product
    PROBAR MEAL Superfood Slam, Net Wt. 3oz.(85g), Film wrapped bar
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1969-2019·2019-07-31

    Probar Chocolate Coconut Bars Recalled for Undeclared Milk and Soy

    Probar LLC is recalling 2,016 Chocolate Coconut bars because they may contain undeclared milk and soy allergens.

    Product
    PROBAR The Simply Real Bar: Chocolate Coconut, Net Wt. 85g, Film wrapped bar
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2011-2019·2019-07-31

    Philips BrightView XCT Medical Device Recalled for Handcontroller Motion Defect

    Philips Medical Systems is recalling 427 BrightView XCT devices because a handcontroller issue may cause uncommanded motions or continued motion after buttons are released.

    Product
    BrightView XCT , Model Number 882482
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2026-2019·2019-07-31

    Siemens AXIOM Artis TC X-ray Generator Recall for Power Supply Issue

    Siemens is recalling one AXIOM Artis TC unit due to a power supply tolerance issue that may cause X-ray generation failure during procedures.

    Product
    AXIOM Artis TC, Model Number 7728350
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2080-2019·2019-07-31

    Bard Nautilus Delta Port Kits Recalled for ECG Signal Loss

    Bard Peripheral Vascular is recalling specific Nautilus Delta Port Kits due to a risk of losing the intravascular ECG signal during placement procedures.

    Product
    POWERPORT CLEARVUE isp, 6F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE isp, 8F CHRONOFLEX Catheter, Intermediate NAUTILUS DELTA Kit; POWERPORT CLEARVUE Slim, 6F CHRONOFLEX Catheter and Suture Plugs, Intermediate NAUTILUS DELTA Kit; POWERPORT…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2039-2019·2019-07-31

    Cardinal Health Recalls Monoject Hypodermic Needles Due to Sterility Barrier Defect

    Cardinal Health is recalling Monoject Standard Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.

    Product
    Monoject Standard Hypodermic Needle, 16 G x 1-1/2" Item code:8881200045
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2025-2019·2019-07-31

    Siemens AXIOM Artis dFC X-ray Generator Recall for Power Supply Issue

    Siemens is recalling 19 AXIOM Artis dFC units because a power supply tolerance issue may cause generator failure, preventing X-ray procedures.

    Product
    AXIOM Artis dFC, Model Number 7727717
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19E052000·2019-07-31

    Vitro Recalls Aftermarket Rear Window Glass for Non-Compliant Fragment Size

    Vitro is recalling 47,366 aftermarket rear window glass units for various vehicles because improper tempering may result in large fragments that increase injury risk in a crash.

    Product
    VISIBILITY:GLASS, SIDE/REAR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2035-2019·2019-07-31

    Spacelabs Smart Disclosure System Recalled for Patient Data Mismatch

    Spacelabs Healthcare is recalling the Smart Disclosure System because patient records were printed with waveforms from other patients.

    Product
    Spacelabs Healthcare Smart Disclosure System, Model 92810, a component of the Intesys Clinical Suite (ICS) G2.
    Category
    Medical Device
    Distribution
    Distributed nationwide