The Recall Desk

State

Northern Mariana Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

59751–59775 of 73856

  • ModerateFDA (Devices)·Z-0708-2014·2014-01-15

    Anspach Recalls Micro Curved Attachments Due to Unclear Directions for Use

    The Anspach Effort, Inc. is recalling MCA Micro Curved Attachments and cutting burrs because the directions for use do not clearly specify intended use for delicate bone in otologic procedures.

    Product
    Multiples Anspach Micro Curved Attachments (MCA) and Curved Burr Support S leves (Cutters and Attachments) MCA - MICRO CURVED ATTACHMENT, MCA5-05SD - 0.5MM DIAMOND BALL, 5.6CM, MCA5-06SD - 0.6MM DIAMOND BALL, 5.6CM, MCA5-07SD - 0.7MM DIAMOND BALL, 5.6CM, MCA5-08SD…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-398-2014·2014-01-15

    Mutual Pharmaceutical Recalls FIBRICOR Tablets Due to Labeling Error

    Mutual Pharmaceutical is recalling FIBRICOR (fenofibric acid) tablets because the patient insert contains incorrect medical advice regarding HDL-C levels.

    Product
    FIBRICOR (fenofibric acid) Tablets, 105 mg, a) 30 count bottle (NDC 13310-102-07), b) 90 count bottle (NDC 13310-102-90), Manufactured for AR SCIENTIFIC, INC, Philadelphia, PA 19124 USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-399-2014·2014-01-15

    Mutual Pharmaceutical Recalls Fenofibric Acid Tablets Due to Labeling Error

    Mutual Pharmaceutical is recalling specific lots of Fenofibric Acid tablets because the patient insert contains incorrect medical advice regarding HDL-C levels.

    Product
    Fenofibric Acid, immediate release tablet, 35 mg, 30 count bottle Rx only, Mutual Pharmaceutical Co., Inc., Philadelphia, PA 19124 USA NDC 53489-677-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-400-2014·2014-01-15

    Mutual Pharmaceutical Recalls Fenofibric Acid Tablets Due to Labeling Error

    Mutual Pharmaceutical is recalling specific lots of Fenofibric Acid tablets because the patient insert contains incorrect medical advice regarding HDL-C levels.

    Product
    Fenofibric Acid, immediate release tablet, 105 mg, a) 30 count bottle (NDC 53489-678-07), b) 90 count bottle (NDC 53489-678-90), Rx only, Mutual Pharmaceutical Co., Inc., Philadelphia, PA 19124 USA
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·14079·2014-01-14

    SRAM Recalls Hydraulic Bicycle Brakes Due to Crash and Injury Hazards

    SRAM is recalling about 25,350 hydraulic road rim and disc brakes for bicycles because the systems can fail, posing a crash and injury hazard.

    Product
    SRAM Hydraulic Road Rim Brakes and Hydraulic Road Disc Brakes for bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14708·2014-01-14

    Arctic Cat Recalls 2014 Snowmobiles Due to Fuel Leak Fire Hazard

    Arctic Cat is recalling about 264 Model Year 2014 500 Sno Pro snowmobiles because fuel can leak from the tank, posing a fire hazard. No injuries have been reported.

    Product
    Arctic Cat snowmobiles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V007000·2014-01-13

    General Motors Recalls 2014-2015 Trucks and SUVs for Engine Fire Risk

    General Motors is recalling specific 2014-2015 Chevrolet, GMC, and Cadillac vehicles because overheated exhaust components may melt plastic parts and cause an engine fire.

    Product
    CHEVROLET — CHEVROLET, GMC, CADILLAC SILVERADO, SIERRA 1500, ESCALADE, YUKON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·001-2014·2014-01-10

    Tyson Recalls Mechanically Separated Chicken Due To Salmonella Heidelberg Contamination

    Tyson Foods is recalling 33,840 pounds of mechanically separated chicken products due to possible Salmonella Heidelberg contamination linked to a cluster of illnesses.

    Product
    Tyson Foods, Inc. — Missouri Firm Recalls Mechanically Separated Chicken Products Due To Possible Salmonella Heidelberg Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·14077·2014-01-09

    New Yorker Boiler Recalls Gas-Fired Hot Water Boilers Due to Carbon Monoxide Hazard

    New Yorker Boiler Company is recalling about 191 gas-fired hot water boilers manufactured between May 2012 and February 2013 because a defective air pressure switch can allow excessive carbon monoxide emissions.

    Product
    Gas-fired hot water boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14076·2014-01-09

    U.S. Boiler Recalls Gas-Fired Hot Water Boilers Due to Carbon Monoxide Hazard

    U.S. Boiler is recalling approximately 26,000 gas-fired hot water boilers in the U.S. and 310 in Canada because a faulty air pressure switch may allow excessive carbon monoxide emissions.

    Product
    Gas-fired hot water boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V004000·2014-01-08

    Glaval Bus Recalls 2010-2013 Models Due to Alternator Harness Pinch Risk

    Glaval Bus is recalling 467 model year 2010-2013 transit buses because a pinched alternator harness may cause vehicle stalling or fire.

    Product
    GLAVAL BUS — GLAVAL BUS, GLAVAL ENTOURAGE, TITAN II, UNIVERSAL, LEGACY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0598-2014·2014-01-08

    Asante Conset Infusion Set Recalled for Tubing Disconnects

    Asante Solutions is recalling Conset Infusion Sets because tubing may disconnect from the connector, causing insulin leakage and under-dosing.

    Product
    Asante Conset Infusion Set with 60cm tubing & 6mm cannula packaged in 5-packs,singles,or inside a Combination Kit (FG-5226-4) Distributed by Asante Solutions, Sunnyvale, CA; Manufactured by Convatec; Lejre, Denmark.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0594-2014·2014-01-08

    Asante Comfort Infusion Set Recalled Due to Tubing Disconnects

    Asante Solutions is recalling 834 Comfort Infusion Sets because tubing may disconnect from the connector, causing insulin leakage and reduced delivery.

    Product
    Asante Comfort Infusion Set with 60cm tubing & 13mm cannula packaged in 5-packs, singles,or inside a Combination Kit (FG-5123-4) Manufactured for: Asante Solutions Sunnyvale, CA; Manufactured by: Unomedical Lejre, Denmark
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-395-2014·2014-01-08

    Hospira Recalls Bupivacaine Hydrochloride Vials Due to Sterility Concerns

    Hospira Inc. is recalling 65,109 vials of Bupivacaine Hydrochloride with Epinephrine due to a potential breach in the aseptic process caused by equipment failure.

    Product
    BUPIVACAINE HYDROCHLORIDE — BUPIVACAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-392-2014·2014-01-08

    Teva Recalls Daunorubicin Hydrochloride Injection Due to Precipitate Presence

    Teva Pharmaceuticals USA is recalling specific lots of Daunorubicin Hydrochloride Injection because the drug product contains precipitate.

    Product
    Daunorubicin Hydrochloride Injection, 20 mg/4 mL (5 mg/mL), 4 mL Single Dose Vial, Rx ONLY, For IV Use Only, Manufactured By: Teva parenteral Medicines, Inc., Irvine, CA NOVAPlus¿¿ labels. NDC 0703-5233-13 (carton), NDC 0703-5233-11 (vial) or NDC 0703-5233-93 (carton), NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0596-2014·2014-01-08

    Asante Comfort Infusion Set Recalled for Tubing Disconnection

    Asante Solutions is recalling 635 Comfort Infusion Sets because the tubing may disconnect from the connector, causing insulin leakage and reduced delivery.

    Product
    Asante Comfort Infusion Set with 110cm tubing & 13mm cannula packaged in 5-packs,singles, or inside a Combination Kit (FG-5143-4). Manufactured for: Asante Solutions Sunnyvale, CA; Manufactured by: Unomedical Lejre, Denmark
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0597-2014·2014-01-08

    Asante Comfort Infusion Set Recalled for Tubing Disconnects

    Asante Solutions is recalling 352 Comfort Infusion Sets because the tubing may disconnect from the connector, causing insulin leakage and reduced delivery.

    Product
    Asante Comfort Infusion Set with 110cm tubing & 17mm cannula packaged in 5-packs, singles, or inside a Combination Kit (FG-5147-4). Manufactured for: Asante Solutions Sunnyvale, CA; Manufactured by: Unomedical, Lejre, Denmark
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0603-2014·2014-01-08

    Terumo Cardiovascular Procedure Kits Recalled Due to Uncleared Safety Valve

    Terumo is recalling 24,227 Custom Cardiovascular Procedure Kits because the Overpressure Safety Valve used in the arterial line was not cleared for that specific use.

    Product
    Terumo Cardiovascular Custom Cardiovascular Procedure Kits containing an Overpressure Safety Valve, LN130B, in the Arterial Recirculation Line
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0617-2014·2014-01-08

    Stryker Secure II Med/Surg Beds Recalled for Potential Cover Damage

    Stryker is recalling Secure II and S3 Med/Surg beds due to potential damage to the Foot End Cover and Power Coil Cable caused by reduced clearance.

    Product
    Secure II Med/Surg Bed Secure II and the 3002 S3 are the beds typically found in the Med-Surg units of the hospitals. The bed is designed for a 15 year expected service life under normal use conditions, and with appropriate periodic maintenance as described in the maintenance…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0607-2014·2014-01-08

    Baxter IntelliFill Pharmacy Compounding Device Recalled for Filtration Defect

    Baxter Healthcare is recalling 28 IntelliFill i.v. Pharmacy Compounding Devices because they may operate with HEPA filtration disabled.

    Product
    IntelliFill i.v. Pharmacy Compounding Device (PCD). Intended to fill syringes from 0.5mL up to 11.5mL using mixing instructions from its formulary to fill the orders.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0595-2014·2014-01-08

    Asante Comfort Infusion Set Recalled for Tubing Disconnection and Insulin Leakage

    Asante Solutions is recalling 246 Comfort Infusion Sets because the tubing may disconnect from the connector, causing insulin leakage and reduced delivery to patients.

    Product
    Asante Comfort Infusion Set with 60cm tubing & 17mm cannula packaged in 5-packs, singles,or inside a Combination Kit (FG-5127-4). Manufactured for: Asante Solutions Sunnyvale, CA; Manufactured by: Unomedical Lejre, Denmark
    Category
    Medical Device
    Distribution
    Distributed nationwide