The Recall Desk

State

Northern Mariana Islands product recalls

73,734 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 73,734 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33851–33875 of 73757

  • ModerateFDA (Drugs)·D-1278-2019·2019-05-22

    Pfizer Recalls Relpax Tablets Due to Incorrect Strength Labeling

    Pfizer is recalling Relpax 40 mg tablets because secondary packaging incorrectly lists the strength as 20 mg. The error is on one side of the carton.

    Product
    Relpax (eletriptan HBr) 40 mg, a) 12 tablets 2 cards x six 40 mg tablets per blister pack, NDC 0049-2340-05; b) 6 tablets 1 card x six 40 mg tablets per blister pack, NDC 0049-2340-45, Rx Only, Made in Ireland, Distributed by Roerig, Division of Pfizer Inc, NY NY 10017.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1366-2019·2019-05-22

    Barlean's Essential Woman Softgels Recalled for Undeclared Sulfites

    Barlean's is recalling Essential Woman softgels due to undeclared sulfites. Sulfite levels in the finished goods do not exceed 10 ppm.

    Product
    Item FG 10146, Barlean s, Essential Woman, 120 count Softgels per bottle, UPC 7 05875 10013 7. Item FG 10147, Barlean s, Essential Woman, 60 count Softgels per bottle, UPC 7 05875 10009 0.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1302-2019·2019-05-22

    CVS Children's Cough Syrup Recalled for Potential B. cepacia Contamination

    Unipharma, LLC is recalling CVS Health Children's Cough Syrup due to potential contamination with B. cepacia bacteria.

    Product
    CVS Health Children's Cough Syrup English Ivy Leaf Daytime Relief Natural Pineapple Flavor 20 Single-Use 0.08 fl. oz. (2.5 mL), Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, UPC 050428597958
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1368-2019·2019-05-22

    Barlean's Full Spectrum Hemp Extract Recalled for Undeclared Sulfites

    Barlean's is recalling Full Spectrum Hemp Extract softgels due to undeclared sulfites. Sulfite levels do not exceed 10 ppm.

    Product
    Item FG 10190, Barleans Full Spectrum Hemp Extract, 60 Softgels per bottle. UPC 7 05875 80113 3. Item FG 10193, Barleans Full Spectrum Hemp Extract, 30 Softgels per bottle. UPC 7 05875 80115 7.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1300-2019·2019-05-22

    CVS Children's Allergy Liquid Recalled for Potential B. cepacia Contamination

    Unipharma is recalling CVS Health Children's Allergy Relief Liquid Medication due to a precautionary measure regarding potential contamination with B. cepacia bacteria.

    Product
    CVS Health Children's Allergy Relief Liquid Medication Diphenhydramine HCl 12.5 mg/5 mL Oral Solution Antihistamine Mixed Berry Flavor 20 Single-Use 0.17 fl. oz. (5 mL), Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI 02895, NDC 69842-261-01, UPC 050428597156
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1356-2019·2019-05-22

    Back Roads Granola Recalled for Potential Aluminum Contamination

    Back Roads Food Company is recalling Maple Pecan Granola because it may contain pieces of aluminum.

    Product
    Back Roads Granola: Maple Pecan Best by date: 01/11/20-02/2/20 In 10 oz, 12 oz, 2.45lb, 3 lb, and 28lb
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1354-2019·2019-05-22

    Back Roads Granola Recalled for Potential Aluminum Contamination

    Back Roads Food Company is recalling specific lots of Coconut Crunch Granola because the products may contain pieces of aluminum.

    Product
    Back Roads Granola: Coconut Crunch Best by date: 01/11/20-02/2/20 In 10 oz, 12 oz, 2.45lb, 3 lb, and 28lb
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1361-2019·2019-05-22

    Barlean's Ultra EPA Fish Oil Recalled for Undeclared Sulfites

    Barlean's is recalling Ultra EPA Fish Oil softgels due to undeclared sulfites. Sulfite levels in the finished goods do not exceed 10 ppm.

    Product
    Item FG 10084, Barlean s, Ultra EPA Fish Oil 1250 mg Omega-3, 60 softgels per bottle, UPC 7 05875 61005 6.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1338-2019·2019-05-22

    Integra Flowable Wound Matrix Recalled for Stability Failure

    Integra Limited is recalling 274 units of Integra Flowable Wound Matrix (Lot 2991332) because the product failed stability testing for visual appearance and force displacement.

    Product
    Integra Flowable Wound Matrix Catalog No: FWD301 Product Usage: Integra Flowable Wound Matrix is indicated for the treatment of tunneling and/or undermined wounds including: surgical wounds (donor sites/grafts, post-Moh s surgery, post-laser surgery, podiatric, wound…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1341-2019·2019-05-22

    Siemens Artis Q Angiography Systems Recalled for Tabletop Movement Blockage

    Siemens Medical Solutions is recalling 459 Artis Q angiography systems because the floating tabletop movement may be blocked after a collision sensor activates.

    Product
    Artis Q (material 10848280, 10848281, 10848282) - Product Usage: AXIOM Artis zee and Q/ Q.zen is a family of dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1366-2019·2019-05-22

    Arrow PICC Recall for Incorrect Length Labeling

    Arrow International is recalling 963 Arrow PICC kits because some are labeled with the wrong length, potentially leading to incorrect clinical use.

    Product
    Arrow PICC powered by Arrow VPS Precision Stylet Product Code:CDC-44052-VPS2 Product Usage: The Arrow Pressure Injectable PICC is indicated for short-term or longterm peripheral access to the central venous system for intravenous therapy, blood sampling, infusion, pressure…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1364-2019·2019-05-22

    Barlean's Olive Leaf Complex Recalled for Undeclared Sulfites

    Barlean's is recalling Olive Leaf Complex softgels due to undeclared sulfites. Sulfite levels do not exceed 10 ppm.

    Product
    Item FG 10106, Barlean s, Olive Leaf Complex, 120 Softgels per bottle. UPC 7 05875 70009 2. Item FG 10107, Barlean s, Olive Leaf Complex, 60 Softgels per bottle. UPC 7 05875 0008 5.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·19124·2019-05-21

    ION Audio Recalls Portable Speakers Due to Explosion Hazard

    ION Audio is recalling four models of portable speakers because hydrogen gas can leak from the battery, causing the speaker to burst and explode.

    Product
    Portable speakers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V383000·2019-05-21

    Honda Recalls 2019 CR-V Vehicles for Steering Wheel Air Bag Defect

    Honda is recalling 2019 CR-V vehicles because burrs on the steering wheel core may damage air bag wiring, potentially disabling the driver's air bag or causing it to deploy unexpectedly.

    Product
    HONDA — HONDA CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V381000·2019-05-20

    Newmar Recalls 2019-2020 Motorhomes Due to Brake Valve Defect

    Newmar is recalling 40 specific 2019 and 2020 motorhomes because a brake relay valve defect may cause extended stopping distances, increasing crash risk.

    Product
    NEWMAR — NEWMAR KING AIRE, LONDON AIRE, ESSEX, DUTCH STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V382000·2019-05-20

    Ducati Recalls Panigale Motorcycles Due to Fuel Tank Pressure Issue

    Ducati is recalling 2018-2019 Panigale motorcycles because excessive fuel tank pressure may cause fuel to spray when opening the cap, increasing injury and fire risks.

    Product
    DUCATI — DUCATI PANIGALE SPECIALE, PANIGALE V4 S, PANIGALE V4, PANIGALE R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V380000·2019-05-19

    Heil AJB9-1040 Hybrid Trailers Recalled for Frame Cracking

    Entrans is recalling 2017-2020 Heil AJB9-1040 Hybrid trailers because frame cracks may develop, affecting handling and increasing crash risk.

    Product
    HEIL — HEIL AJB9-1040 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V379000·2019-05-17

    Newell Recalls 2017-2020 P50 Motorcoaches Due to Wiper Linkage Defect

    Newell Coach Corp. is recalling 2017-2020 P50 motorcoaches because a short wiper arm linkage may cause the wiper to rotate downward, reducing visibility and increasing crash risk.

    Product
    NEWELL — NEWELL P50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V376000·2019-05-16

    Micro Bird Recalls 2018-2019 School Buses for Solenoid Overheating Risk

    Micro Bird is recalling 2018-2019 G5 and T-Series school buses because a heavy-duty solenoid may overheat nearby components, potentially causing vehicle stoppage or fire.

    Product
    MICRO BIRD — MICRO BIRD T-SERIES SCHOOL BUS, G5 TRANSIT BUS, G5 SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V378000·2019-05-16

    Honda and Acura Recall Vehicles Due to Passenger Air Bag Defect

    Honda is recalling 19,138 vehicles because the front passenger air bag inflator may be installed incorrectly, potentially preventing proper deployment in a crash.

    Product
    HONDA — HONDA, ACURA INSIGHT, CIVIC, ACCORD CROSSTOUR, CIVIC GX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1277-2019·2019-05-15

    Alvogen Recalls Fentanyl Transdermal Systems Due to Product Mix-Up

    Alvogen is recalling Fentanyl Transdermal Systems because a customer reported a carton labeled 12 mcg/h contained 50 mcg/h patches.

    Product
    FENTANYL SYSTEM — FENTANYL SYSTEM (FENTANYL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1272-2019·2019-05-15

    Zydus Recalls Acyclovir Tablets Due to Labeling Error with Carvedilol

    Zydus Pharmaceuticals is recalling Acyclovir 400 mg tablets because one bottle was found to contain Carvedilol 6.25 mg tablets due to a label mix-up.

    Product
    ACYCLOVIR — ACYCLOVIR (ACYCLOVIR)
    Category
    Drug
    Distribution
    Distributed nationwide