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.

44676–44700 of 73832

  • LowUSDA FSIS·007-2017·2017-01-18

    Willow Tree Poultry Farm Recalls Misbranded Chicken Salad Products

    Willow Tree Poultry Farm is recalling 204 pounds of chicken salad products because they are misbranded as chicken salad but contain egg salad.

    Product
    WILLOW TREE POULTRY FARM, INC. — Willow Tree Poultry Farm, Inc. Recalls Chicken Salad Products Due To Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0424-2017·2017-01-18

    Pfizer Recalls Cytotec Tablets Due to Failed Impurity Specifications

    Pfizer is recalling 1,706 cartons of Cytotec (misoprostol) tablets nationwide because the product failed impurity and degradation specifications.

    Product
    CYTOTEC — CYTOTEC (MISOPROSTOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V037000·2017-01-17

    Highland Ridge RV Recalls 2017 Fifth Wheels and Travel Trailers for Gas Leak Risk

    Highland Ridge RV is recalling 2017 Open Range, Mesa Ridge, and Roamer models because the outside range can be stored with the gas valve open, creating a fire or explosion hazard.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT, HIGHLAND RIDGE FW ROAMER, OPEN RANGE, MESA RIDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V034000·2017-01-13

    Renegade RV Recalls Motorhomes Due to Seat Belt Anchorage Defect

    REV Recreation Group is recalling specific Renegade RV motorhomes because seat belt anchorage hardware may pull out of the floor framing during a crash.

    Product
    RENEGADE RV — RENEGADE RV CORE, SPECIALTY SPRINTER, VIENNA, VILLAGIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17728·2017-01-12

    Nantucket Distributing Recalls Pre-Lit Christmas Trees Due to Fire Hazard

    Nantucket Distributing is recalling pre-lit artificial Christmas trees because the fuse can overheat and blow, posing a fire hazard. No injuries have been reported.

    Product
    Pre-Lit Globe Light Christmas trees
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17726·2017-01-12

    BRP Recalls Side-by-Side Off-Road Vehicles Due to Roll-Away Hazard

    BRP is recalling about 780 Can-Am Defender side-by-side off-road vehicles because they can unexpectedly roll away while in park, posing an injury risk.

    Product
    Side-by-side off-road vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V033000·2017-01-12

    GM Recalls 2016-2017 Chevrolet Suburban HD for Incorrect Rearview Mirror

    General Motors is recalling 2016-2017 Chevrolet Suburban HD vehicles equipped with a convex right-hand outside mirror instead of a non-convex one, which may cause drivers to misjudge distance.

    Product
    CHEVROLET — CHEVROLET SUBURBAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17068·2017-01-12

    Boosted Recalls Electric Skateboards Due to Fire Hazard

    Boosted Inc. is recalling 2nd Generation Dual+ electric skateboards because the lithium ion battery packs can overheat and smoke, posing a fire hazard.

    Product
    Electric-powered skateboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·17067·2017-01-11

    Bad Boy Off-Road Utility Vehicles Recalled Due to Missing Seat Belts

    Textron Specialized Vehicles is recalling about 1,100 Bad Boy off-road utility vehicles because they lack seat belts, posing a risk of serious injury or death.

    Product
    Bad Boy off-road utility vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0366-2017·2017-01-11

    Wells Pharmacy Recalls Methylcobalamin Injectable Due to Sterility Concerns

    Wells Pharmacy Network LLC is recalling 265 vials of compounded Methylcobalamin 5,000 mcg/mL Injectable because the product lacks assurance of sterility.

    Product
    Methylcobalamin 5,000 mcg/mL Injectable, 10 mL vial, Compounded by Wells Pharmacy, Ocala, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0345-2017·2017-01-11

    Wells Pharmacy Recalls Ceftazidime Ophthalmic Kits Due to Sterility Concerns

    Wells Pharmacy Network LLC is recalling 46 kits of compounded Ceftazidime Ophthalmic 2.25% due to a lack of assurance of sterility.

    Product
    Ceftazidime, Lyophilized, Ophthalmic 2.25% Kit, Rx only, Compounded by Wells Pharmacy, Ocala , FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0320-2017·2017-01-11

    Tri-Coast Pharmacy Recalls TriMix Injection Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 2 units of TriMix injection because the agency cannot assure the products are sterile.

    Product
    TriMix, Alprostadil/Phentolamine/Papaverine 100mcg/3mg/30mg/mL, (1 ML). Compounded by Tri-Coast Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0268-2017·2017-01-11

    Tri-Coast Pharmacy Recalls L-Tyrosine Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 50 vials of compounded L-Tyrosine 10 mg/mL because the products lack assurance of sterility.

    Product
    L-Tyrosine 10 mg/mL, (30 ML). Compounded by Tri-Coast Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0421-2017·2017-01-11

    Wells Pharmacy Recalls Vitamin D3 Injectable Due to Sterility Concerns

    Wells Pharmacy Network LLC is recalling 335 vials of Vitamin D3 in Sesame Oil Injectable due to a lack of assurance of sterility.

    Product
    Vitamin D3 in Sesame Oil Injectable 50,000 IU/mL, 5 mL vial, Compounded by Wells Pharmacy, Ocala, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0294-2017·2017-01-11

    Tri-Coast Pharmacy Recalls Sermorelin GT Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 920 vials of compounded Sermorelin GT nationwide due to a lack of assurance of sterility.

    Product
    Sermorelin GT (Sermorelin Acetate 15 mg/GHRP-2 5.4 mg/Theanine (L) 75 mg). Compounded by Tri-Coast Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0266-2017·2017-01-11

    Tri-Coast Pharmacy Recalls L-Arginine HCL Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 41 vials of compounded L-Arginine HCL 100 mg/mL because there is a lack of assurance of sterility. The products were distributed nationwide.

    Product
    L-Arginine HCL 100 mg/mL, (30 ML). Compounded by Tri-Coast Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0287-2017·2017-01-11

    Tri-Coast Pharmacy Recalls Sermorelin Acetate Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 260 vials of Sermorelin Acetate 6 mg compounded between May and November 2016 because the agency cannot assure the products are sterile.

    Product
    Sermorelin Acetate 6 mg. Compounded by Tri-Coast Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0418-2017·2017-01-11

    Wells Pharmacy Recalls Trimix Injectable Due to Sterility Concerns

    Wells Pharmacy Network LLC is recalling specific vials of Trimix Injectable because the agency could not ensure the product was sterile.

    Product
    Trimix Injectable 30 mg/3 mg/60 mcg/mL, a) 2 mL, b) 5 mL and c) 10 mL vials, Compounded by Wells Pharmacy, Ocala, FL
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0299-2017·2017-01-11

    Tri-Coast Pharmacy Recalls Testosterone Cypionate Due to Sterility Concerns

    Tri-Coast Pharmacy is recalling 2,818 vials of compounded Testosterone Cypionate in Grapeseed nationwide due to a lack of assurance of sterility.

    Product
    Testosterone Cypionate in Grapeseed, 200 mg/mL, (5 ML and 10 ML). Compounded by Tri-Coast Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide