The Recall Desk

State

Northern Mariana Islands product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43176–43200 of 73829

  • ModerateFDA (Drugs)·D-0860-2017·2017-05-31

    Mylan Recalls Tarina Fe 1/20 Tablets Due to Chemical Contamination

    Mylan Pharmaceuticals is recalling Tarina Fe 1/20 tablets due to chemical contamination from paint thinner vapors during manufacturing.

    Product
    Tarina Fe 1/20 (Norethindrone Acetate and Ethinyl Estradiol Tablets, USP and Ferrous Fumarate Tablets), 1 blister pack containing 28 tablets (NDC 50102-128-01), packaged in 3 pouches, each pouch contains one blister pack of 28 tablets (NDC 50102-128-03), Rx only, Manufactured…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2120-2017·2017-05-31

    Bard StatLock IV Premium Catheter Stabilization Device Recalled for Sizing Error

    Bard Access Systems is recalling 4,500 units of StatLock IV Premium Catheter Stabilization Devices because they may contain incorrectly sized retainer clips.

    Product
    StatLock¿ IV Premium Catheter Stabilization Device, product code IV0570. sterile. Packaging: packaged as single units in tyvek to film pouches, the product is distributed in cartons containing 25 devices and cases containing 250 devices.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2124-2017·2017-05-31

    Beckman Coulter Recalls Microalbumin Reagent Due to Potential Out-of-Range Recovery

    Beckman Coulter is recalling Microalbumin Reagent Lot M609458 because it may recover outside the lower limit of the published insert range for Urine Protein Control Level 1.

    Product
    Microalbumin Reagent, Catalog No. 475100, Product Labeling A18520AL MA reagent, when used in conjunction with UniCel DxC 600/800 System(s) and SYNCHRON¿ Systems MA Calibrator, is intended for quantitative determination of Albumin concentration in human urine
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0840-2017·2017-05-31

    Advanced Pharma Recalls Atropine Sulfate for Latex Labeling Defect

    Advanced Pharma Inc. is recalling all lots of Atropine Sulfate because the product may contain latex but lacks appropriate labeling.

    Product
    Atropine Sulfate all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0837-2017·2017-05-31

    Advanced Pharma Recalls Esmolol HCl Due to Latex Labeling Defect

    Advanced Pharma Inc. is recalling all Esmolol HCl products because the labeling does not indicate that the products may contain synthetic or natural latex.

    Product
    Esmolol HCl all strengths, all dosage forms and all packaging, Rx Only, Avella of Houston, Houston, TX 77054
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-2250-2017·2017-05-31

    Schiff Move Free Advanced Tablets Recalled for Incorrect Packaging

    RB Manufacturing is recalling Schiff Move Free Advanced Plus MSM & Vitamin D3 tablets due to incorrect packaging.

    Product
    Schiff Move Free Advanced Plus MSM & Vitamin D3 with Glucosamine + Chondroitin, 80 Coated Tablets, Dietary Supplement, Product item number: 20525-11873
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0857-2017·2017-05-31

    Sun Pharmaceutical Recalls Children's Cetirizine Tablets for Hardness Issues

    Sun Pharmaceutical Industries is recalling 13,200 bottles of Children's Cetirizine Hydrochloride Chewable Tablets due to out-of-specification tablet hardness.

    Product
    Children's Cetirizine Hydrochloride Chewable Tablets, 5 mg, 30-count bottle, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol - 389 350, Gujarat, India; Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 47335-343-83.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2121-2017·2017-05-31

    Medtest Recalls Pointe Scientific Chemistry Controls Due to Mean Assignment Error

    Medtest Holdings is recalling Pointe Scientific Chemistry Controls Level I and II because the original mean assigned to the controls was too high, resulting in a new assigned mean outside the published range.

    Product
    Pointe Scientific Chemistry Controls Level I and II LEVl: Amber glass vial w/PP white plastic cap. LEV2: Amber glass vial w/PP black plastic cap.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0858-2017·2017-05-31

    Strides Pharma Recalls Benzonatate Capsules for Stability Failure

    Strides Pharma Inc. is recalling Benzonatate capsules due to out-of-specification preservative levels. The FDA classified this as a Class III recall.

    Product
    BENZONATATE — BENZONATATE (BENZONATATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0859-2017·2017-05-31

    Qualitest Recalls Hydrocortisone Lotion for Excessive Potency

    Qualitest Pharmaceuticals is recalling 109,620 bottles of Hydrocortisone Lotion, USP, 2.5% because the product is superpotent, meaning it contains more active ingredient than specified.

    Product
    HYDROCORTISONE LOTION, USP, 2.5%, 2 FL OZ (59 mL) bottle, Rx only, Manufactured for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-7785-52.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowNHTSA·17V352000·2017-05-31

    Volkswagen Recalls 2017 Jetta for VIN Marking Mismatch

    Volkswagen is recalling 2017 Jetta vehicles because the VIN on the body does not match the VIN plate near the windshield, violating federal certification regulations.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V348000·2017-05-30

    Pierce Fire Trucks Recalled for Rear Axle Shaft Defect

    Pierce Manufacturing is recalling 1999-2013 fire trucks with electric All-steer rear steering due to improperly heat-treated axle shafts that may break.

    Product
    PIERCE — PIERCE QUANTUM, ARROW XT, VELOCITY, ENFORCER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V347000·2017-05-30

    KZRV Venom Travel Trailer Recall for Fire Risk

    KZRV is recalling 2016-2018 Venom fifth-wheel travel trailers with outside kitchens because a missing copper pipe may cause the gas line to melt and start a fire.

    Product
    KZRV — KZRV VENOM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V350000·2017-05-30

    Jayco Eagle Travel Trailer Recalled for Incorrect Weight Rating Label

    Jayco is recalling 2018 Eagle TT 330RSTS trailers because the Federal Placard lists an incorrect Gross Axle Weight Rating, which could lead to overloading and loss of control.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V345000·2017-05-26

    VanLeigh Recalls 2015-2018 Vilano Trailers Due to Spare Tire Winch Defect

    VanLeigh is recalling 2015-2018 Vilano fifth-wheel recreational trailers because the spare tire winch may not be properly fastened, posing a crash risk if the tire falls off.

    Product
    VANLEIGH — VANLEIGH VILANO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V344000·2017-05-26

    Gulf Stream Travel Trailer Recall for Incorrect Tire Identification Label

    Gulf Stream is recalling 2015-2018 Vista and Vintage Cruiser travel trailers because the tire label lists incorrect tire specifications, which could lead to installing the wrong replacement tires.

    Product
    GULF STREAM — GULF STREAM VISTA CRUISER, VINTAGE CRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17168·2017-05-26

    CPSC Recalls Kobalt and Greenworks Cordless Lawn Mowers Due to Fire Hazard

    CPSC is recalling about 28,000 Kobalt and Greenworks cordless electric lawn mowers because the circuit board can short circuit and catch fire. No injuries have been reported.

    Product
    Cordless electric lawn mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V346000·2017-05-26

    Forest River Recalls 2016-2017 Vibe Trailers for Incorrect Tire Placard

    Forest River is recalling 2016-2017 Vibe recreational trailers because the Federal Placard lists incorrect tire size and pressure information, which could lead to improper tire maintenance.

    Product
    FOREST RIVER — FOREST RIVER VIBE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V340000·2017-05-25

    Eldorado Amerivan 10 Recall for Potential Trailing Arm Mount Failure

    Eldorado Mobility is recalling 2017 Amerivan 10 lowered-floor vehicles because trailing arm mounts may break, potentially causing loss of steering control.

    Product
    ELDORADO — ELDORADO AMERIVAN 10
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V341000·2017-05-25

    Jaguar Recalls 2018 F-TYPE for Turn Signal Reminder Defect

    Jaguar is recalling 2018 F-TYPE vehicles with Highline headlamps because the turn signal reminder may not flash or chime faster if a signal fails, increasing crash risk.

    Product
    JAGUAR — JAGUAR F-TYPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17167·2017-05-25

    Extech Recalls Digital Clamp Meters Due to Electrocution Hazard

    Extech is recalling specific digital clamp meters because they may display incorrect voltage readings, posing an electrocution risk to operators.

    Product
    Digital clamp meters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0748-2017·2017-05-24

    Key Pharmacy Recalls Sterile Compounded Injection Due to Sterility Concerns

    Key Pharmacy and Compounding Center is recalling TRI MIX 40/30/4 injection vials because the firm cannot assure the sterility of the product.

    Product
    TRI MIX 40/30/4 5ML MDV MCG/MG/MG/ML INJ, Injection, 40mcg/30mg/4mg/mL, Rx only, 5 mL Glass/Multiple Dose vial, Prepared by Key Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0745-2017·2017-05-24

    Key Pharmacy Recalls Sterile Compounded Drug Vials Due to Sterility Concerns

    Key Pharmacy and Compounding Center is recalling 17 vials of TRI MIX 20/30/2 injection due to a lack of assurance of sterility.

    Product
    TRI MIX 20/30/2 5ML MDV MCG/MG/MG/1ML INJ, Injection, 20mcg/30mg/2mg/mL, Rx only, 5 mL Glass/Multiple Dose vial , Prepared by Key Compounding Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide