The Recall Desk

State

Northern Mariana Islands product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33351–33375 of 73745

  • ModerateFDA (Drugs)·D-1404-2019·2019-06-19

    Synthetopes Recalls Sn-DTPA Kit Due to Lack of Processing Controls

    Synthetopes Inc is recalling 82 vials of Sn-DTPA Kit 10 mg nationwide due to a lack of processing controls.

    Product
    Sn-DTPA Kit 10 mg, DTPA, Not for Direct Injection, Store at Room Temperature, Synthetopes, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1343-2019·2019-06-19

    B. Braun Recalls Heparin Sodium Bags Due to Low Potency

    B. Braun Medical Inc. is recalling 40,176 bags of Heparin Sodium in Dextrose because testing showed the drug had lower potency than required by USP specifications.

    Product
    HEPARIN SODIUM IN DEXTROSE — HEPARIN SODIUM IN DEXTROSE (HEPARIN SODIUM AND DEXTROSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1771-2019·2019-06-19

    Philips Patient Information Center iX Recall for Infusion Pump Data Accuracy

    Philips is recalling Patient Information Center iX software because infusion pump data may be recorded at 100 times the actual rate.

    Product
    Philips Patient Information Center iX configured with a regional setting which uses a comma for a decimal separator: 866389 Patient Information Center iX B.01 (or later); 866390 Patient Information Center iX B.01 upgrade (or later) Product Usage: The intended use of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1400-2019·2019-06-19

    Synthetopes Recalls Sn-DMSA Solution Due to Processing Control Deficiencies

    Synthetopes Inc. is recalling Sn-DMSA solution vials nationwide due to a lack of processing controls. The product is not for direct injection.

    Product
    Sn-DMSA solution, Store Frozen, Not for Direct Injection, Synthetopes, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1772-2019·2019-06-19

    Philips IntelliBridge System Recall for Infusion Pump Data Storage Accuracy Issues

    Philips is recalling IntelliBridge Systems configured with comma decimal separators because infusion pump data may be recorded at 100 times the actual values.

    Product
    Philips IntelliBridge System configured with a regional setting which uses a comma for a decimal separator: 866417 IntelliBridge System C.01 (or later) 866418 IntelliBridge System C.01 upgrade (or later) Product Usage: The IntelliBridge System is indicated for use in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1406-2019·2019-06-19

    Synthetopes Recalls Sn-Pyrophosphate Kits Due to Processing Control Issues

    Synthetopes Inc. is recalling Sn-Pyrophosphate Kits because of a lack of processing controls. The recall covers all lots remaining within their expiry dates.

    Product
    Sn-Pyrophosphate Kit, 11.9 mg sodium pyrophosphate, Not for Direct Injection, Store at Room Temperature, Synthetopes, Inc.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-1456-2019·2019-06-19

    Laird Superfood Performance Mushrooms Recalled for Iron Labeling Error

    Laird Superfood is recalling Performance Mushrooms because the label incorrectly lists 14 mg of Iron instead of the actual 14 mcg.

    Product
    Performance Mushrooms product is dried mushroom blend of 4 different mushroom mycelial biomass powders cultured on certified organic oats, brand Laird Superfood, uses as Beverage Booster and Functional Fuel Supplement. Product is packaged in 3.17 oz (90 gram) stand up with…
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1396-2019·2019-06-19

    Bausch & Lomb Recalls Lotemax Ophthalmic Gel for Viscosity Issues

    Bausch & Lomb is recalling Lotemax ophthalmic gel because it failed stability specifications for viscosity. The recall covers 17,083 bottles distributed nationwide.

    Product
    LOTEMAX — LOTEMAX (LOTEPREDNOL ETABONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V467000·2019-06-18

    Isuzu Recalls 2018-2020 FTR and Chevrolet 6500XD for Steering Defect

    Isuzu is recalling 2018-2020 FTR and Chevrolet 6500XD vehicles because a steering stopper bolt jam nut may loosen, increasing the turning radius and crash risk.

    Product
    ISUZU — ISUZU, CHEVROLET FTR, 6500XD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V463000·2019-06-18

    Farber Recalls 2017 Ford F-550 Vehicles Due to Brake Light Wiring Issue

    Farber Specialty Vehicles is recalling 2017 Ford F-550s with Whelen brake lights that may illuminate without the brake pedal being pressed, potentially confusing other drivers.

    Product
    FREIGHTLINER — FREIGHTLINER redundant FORD F550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V466000·2019-06-18

    SVO Group Recalls 2017-2018 Ford E-350 and E-450 Shuttle Buses

    SVO Group is recalling 2017-2018 Ford E-350 and E-450 shuttle buses because backup camera images may reverse, increasing crash risk.

    Product
    FORD — FORD E-450, E-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V464000·2019-06-18

    Farber Recalls 2018 International 4300 Vehicles with Whelen Brake Lights

    Farber Specialty Vehicles is recalling 2018 International 4300 SBA vehicles equipped with Whelen brake lights that may illuminate without the brake pedal being pressed.

    Product
    INTERNATIONAL — INTERNATIONAL 4300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V455000·2019-06-17

    Altec Recalls 2017-2018 Aerial Devices Due to Fastener Failure Risk

    Altec is recalling 2017-2018 aerial devices because fasteners securing the rotation bearing may break, potentially causing the pedestal to separate from the turntable.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V454000·2019-06-17

    Forest River Berkshire Motorhomes Recalled for Block Heater Fire Risk

    Forest River is recalling 2017-2018 Berkshire motorhomes because water in the block heater cable can cause corrosion, leading to overheated wiring and fire risk.

    Product
    FOREST RIVER — FOREST RIVER BERKSHIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V462000·2019-06-14

    Caterpillar Recalls 2015-2019 Progress Rail Sky Trim Hi-Rail Vehicles

    Caterpillar is recalling 2015-2019 Progress Rail Sky Trim Hi-Rail vehicles because a support plate may block driver visibility and the boom may detach from the cradle while in motion.

    Product
    PROGRESSIVE RAIL SERVICES — PROGRESSIVE RAIL SERVICES SKY TRIM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·069-2019·2019-06-14

    Ruiz Foods Recalls Bacon Breakfast Wraps Due to Foreign Matter Contamination

    Ruiz Foods is recalling approximately 246,514 pounds of frozen bacon breakfast wraps due to possible contamination with small rocks.

    Product
    Ruiz Food Products, Inc. — Ruiz Foods Products Inc. Recalls Bacon Breakfast Wrap Products Due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·065-2019 EXP·2019-06-14

    Table 87 Frozen Recalls Pork and Beef Pizza Products Lacking Federal Inspection

    Table 87 Frozen, LLC is recalling frozen pork and beef pizza products produced without federal inspection. No adverse reactions have been reported.

    Product
    Table 87 Frozen, LLC — Table 87 Frozen, LLC Recalls Pork and Beef Pizza Products Produced without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V457000·2019-06-14

    Mercedes-Benz Recalls AMG GT Vehicles for Driveshaft Separation Risk

    Mercedes-Benz is recalling 2016-2017 AMG GT vehicles because the carbon-fiber driveshaft may separate, causing a loss of drive and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V456000·2019-06-14

    Autocar Recalls 2013-2018 Xpeditor Vehicles for Drive Shaft Support Defect

    Autocar is recalling 2013-2018 Xpeditor vehicles because the drive shaft support cross member may fail, increasing crash risk. Dealers will install additional support brackets free of charge.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V451000·2019-06-14

    Gillig Low Floor Vehicles Recalled for Glass Roof Hatch Shattering Risk

    Gillig is recalling 2018-2019 Low Floor vehicles because temperature and vibration stresses may cause the tempered glass roof hatch to shatter, potentially injuring passengers.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide