The Recall Desk

State

Northern Mariana Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

56276–56300 of 73850

  • LowFDA (Drugs)·D-0244-2015·2014-11-12

    Apotex Recalls Candesartan Cilexetil Tablets Due to Impurity Failures

    Apotex Inc. is recalling Candesartan Cilexetil Tablets, 32 mg, because out-of-specification results were observed for specific impurities and total impurities.

    Product
    Candesartan Cilexetil Tablets, 32 mg, a) 30-count bottle (NDC 60505-3621-3) b) 90-count bottles (NDC 60505-3621-9) Rx Only, Manufactured by Apotex Research Pvt. Ltd., Bangalore- 560 099, India, Manufactured for Apotex Corp., Weston, FL 33326
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0239-2015·2014-11-12

    Physicians Total Care Recalls Loratadine Tablets Due to Chipped or Broken Pieces

    Physicians Total Care is recalling specific lots of Loratadine 24 HR-OTC 10 mg tablets because they may contain chipped or broken pieces.

    Product
    Loratadine 24 HR-OTC,10 mg, 30-count bottle, Manufactured by Novartis Consumer Health, Parsippany, NJ 07054, Distributed by Physicians Total Care, Tulsa OK 74146, NDC 54868-5268-00
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V722000·2014-11-10

    Kenworth Heavy Trucks Recalled for Undersized Wire Gauge Fire Risk

    PACCAR is recalling 2015 Kenworth heavy trucks because an undersized wire in the instrument panel harness may overheat, increasing the risk of a vehicle fire.

    Product
    KENWORTH — KENWORTH T660, T800, W900, C500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V717000·2014-11-10

    Daimler Recalls 2014-2015 Freightliner Trucks Due to Brake Valve Defect

    Daimler is recalling 2014-2015 Freightliner trucks because defective air brake valves may reduce braking performance and increase crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER 122SD, ARGOSY, CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V719000·2014-11-10

    GM Recalls 2015 Trucks and SUVs for Power Steering Loss

    General Motors is recalling 2015 Chevrolet and GMC vehicles because a steering module defect may cause sudden loss of power assist, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, GMC SUBURBAN, YUKON, TAHOE, SILVERADO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15021·2014-11-10

    McDonald's Recalls Hello Kitty Whistles Due to Choking Hazard

    McDonald's is recalling Hello Kitty Birthday Lollipop Whistles because internal components can detach, posing choking and aspiration risks to young children.

    Product
    Hello Kitty® Birthday Lollipop Whistles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V718000·2014-11-10

    Sutphen Aerial Devices Recalled for Potential Ladder Cable Failure

    Sutphen is recalling 2000-2014 aerial devices because a cable failure could cause the ladder to collapse, increasing injury risk.

    Product
    SUTPHEN — SUTPHEN SPH 100, SP 110, SAI 110, SPI 112
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V712000·2014-11-07

    Forest River Recalls 2015 Wildwood and Salem Trailers for Draw Bar Defect

    Forest River is recalling 2015 Wildwood and Salem Ice Cabin trailers because the draw bar may break, potentially causing the trailer to detach from the vehicle.

    Product
    FOREST RIVER — FOREST RIVER WILDWOOD, SALEM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V716000·2014-11-07

    PACCAR Recalls Kenworth and Peterbilt Trucks Due to Brake Valve Defect

    PACCAR is recalling specific 2014-2015 Kenworth and Peterbilt trucks because defective parking brake valves may reduce braking performance and increase crash risk.

    Product
    KENWORTH — KENWORTH, PETERBILT K270, 220, K370, MODEL 220
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V711000·2014-11-07

    Dodge Journey Recall for Inaccurate Tire Placard Weight Information

    Chrysler is recalling 2014-2015 Dodge Journey vehicles because tire placard labels may contain inaccurate weight and seating information, increasing crash risk.

    Product
    DODGE — DODGE JOURNEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V713000·2014-11-07

    Hyundai Recalls Genesis and Equus Vehicles for Stop Lamp Circuit Failure

    Hyundai is recalling 2009-2011 Genesis and 2011 Equus vehicles because a circuit failure may prevent stop lamps from illuminating, increasing the risk of a rear-end crash.

    Product
    HYUNDAI — HYUNDAI EQUUS, GENESIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0230-2015·2014-11-05

    FDA Recalls Calcium Glucosate Injection Due to Microbial Contamination

    Specialty Compounding, LLC is recalling Calcium Gluconate 2 gm in 100 mL Sodium Chloride 0.9% for Injection due to non-sterility and microbial contamination.

    Product
    CALCIUM GLUCONATE 2 gm (PF) PRESERVATIVE FREE in 100 mL Sodium Chloride 0.9% for Injection, Rx Only Manufactured by Specialty Compounding, 211 S. Bell Blvd, Cedar Park, TX 78613
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0071-2015·2014-11-05

    Martin Avenue Pharmacy Recalls Cromolyn Sodium Inhalant Solution

    Martin Avenue Pharmacy is voluntarily recalling Cromolyn sodium 1% inhalant solution due to sterility assurance concerns identified during an FDA inspection.

    Product
    Cromolyn sodium 1% inhalant solution packaged in a 3 mL or 7 mL vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0085-2015·2014-11-05

    Martin Avenue Pharmacy Recalls Compounded Sterile Preparations Due to Sterility Concerns

    Martin Avenue Pharmacy is voluntarily recalling compounded sterile preparations, including Hyaluronidase base vehicle, due to quality control issues affecting sterility assurance.

    Product
    Hyaluronidase base vehicle (PF) solution packaged in an amber glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0111-2015·2014-11-05

    Martin Avenue Pharmacy Recalls Compounded Sterile Preparations Due to Sterility Concerns

    Martin Avenue Pharmacy is voluntarily recalling compounded sterile preparations, including PGE 1, due to quality control observations that risk sterility assurance.

    Product
    PGE 1, 40 mcg/mL injectable packaged in a clear glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0137-2015·2014-11-05

    Martin Avenue Pharmacy Recalls Compounded Sterile Preparations Due to Sterility Concerns

    Martin Avenue Pharmacy is voluntarily recalling all compounded sterile preparations within expiry due to quality control observations that present a risk to sterility assurance.

    Product
    Tacrolimus oil 0.03% opthalmic solution packaged in an opaque squeeze bottle eye dropper, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0058-2015·2014-11-05

    Martin Avenue Pharmacy Recalls Atropine Sulfate Eye Drops for Sterility Concerns

    Martin Avenue Pharmacy is voluntarily recalling Atropine sulfate 0.01% ophthalmic solution due to quality control issues that may compromise sterility.

    Product
    Atropine sulfate 0.01% opthalmic solution packaged in a squeeze bottle eye dropper, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V702000·2014-11-05

    Wabash National Van Trailer Recall for Cracking Pivot Bolts

    Wabash is recalling 2013 Van trailers because certain pivot bolts may crack, potentially causing the axle to separate and increasing crash risk.

    Product
    WABASH NATIONAL — WABASH NATIONAL VAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0088-2015·2014-11-05

    Martin Avenue Pharmacy Recalls Compounded Sterile Preparations Due to Sterility Concerns

    Martin Avenue Pharmacy is voluntarily recalling compounded sterile preparations, including hydromorphone/clonidine/bupivacaine, due to quality control observations that risk sterility assurance.

    Product
    Hydromorphone/clonidine/bupivacaine 12 mg/600 mcg/0.2 mg/mL injectable packaged in 30 mL or 60 mL syringes, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
    Category
    Drug
    Distribution
    Distributed nationwide