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.

45676–45700 of 73832

  • HighFDA (Devices)·Z-0348-2017·2016-11-09

    Maquet HCU 30 Heater-Cooler Units Recalled for Bacterial Contamination Risk

    Maquet Cardiovascular is recalling 305 HCU 30 units because contaminated water, including Mycobacteria, may enter the device circuits.

    Product
    Heater Cooler Unit Usage: The Heater-Cooler Unit (HCU 30) supplies temperature-controlled water for cardioplegia heat exchangers and for blood heat exchangers in extra corporeal circulation and for blankets with which patients can be warmed or cooled. The HCU 30 is intended…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0350-2017·2016-11-09

    Smith & Nephew Recalls Tandem Hip Shells With Out-of-Specification Grooves

    Smith & Nephew is recalling 2,352 Tandem hip shells manufactured with out-of-specification retainer grooves. The recall covers units distributed nationwide and in 23 other countries.

    Product
    TANDEM (TM) COCR SHELL UHMWPE LINER BIPOLAR, REF NUMBERS: 71322040, 71322041, 71322042, 71322043, 71322044, 71322045, 71322046, 71322047, 71322048, 71322049, 71322050, 71322051, 71322052, 71322053, 71322054, 71322055, 71322057
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0353-2017·2016-11-09

    Hospira Recalls Symbiq Infusion Pumps Due to Backup Battery Failure

    Hospira is recalling 20,311 Symbiq One Channel Infusion Pumps due to a backup battery failure caused by incorrect component installation on some power supply boards.

    Product
    Symbiq One Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids; Product List Number 16026
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0351-2017·2016-11-09

    Smith & Nephew Recalls Tandem Hip Shells With Out-of-Specification Grooves

    Smith & Nephew is recalling 5,806 Tandem hip shell units manufactured with out-of-specification retainer grooves. The recall covers distribution in the US and 23 other countries.

    Product
    TANDEM (TM) INTL COCR SHELL UHMWPE LINER BIPOLAR, REF NUMBERS: 71324038, 71324039, 71324040, 71324041, 71324042, 71324043, 71324044, 71324045, 71324046, 71324047, 71324048, 71324049, 71324050, 71324051, 71324052, 71324053, 71324054, 71324055, 71324057, 71324059, 71325039…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0329-2017·2016-11-09

    Azer Scientific Recalls Glucose Tolerance Beverage Due to Microbiological Test Failures

    Azer Scientific, Inc. is recalling 426 cases of Orange Glucose Tolerance Beverage due to out-of-specification microbiological test results.

    Product
    Glucose Tolerance Beverage- Orange 50 gram Concentration, Liquid 4/Pack of 6 bottles, 24/case Accessory to an In Vitro Diagnostic Oral Glucose Tolerance Test (OGTT) in the evaluation of diabetes mellitus and related disease conditions. Oral Glucose Tolerance Drinks provide a…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0124-2017·2016-11-09

    Akorn Recalls Subpotent Sodium Chloride Ophthalmic Solution

    Akorn Inc. is recalling 29,972 bottles of 5% Sodium Chloride Ophthalmic Solution because the product concentration is less than the labeled amount.

    Product
    Sodium Chloride Ophthalmic Solution, USP, 5%, 15 mL (0.5 fL oz.) bottle, Akorn, Inc., Lake Forest, IL 60045, NDC 17478-623-12.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0119-2017·2016-11-09

    Par Pharmaceutical Recalls Subpotent Gildess 1.5/30 Oral Contraceptive Tablets

    Par Pharmaceutical is recalling Gildess 1.5/30 tablets because they contain subpotent levels of ethinyl estradiol. The recall covers specific lots distributed nationwide and in Puerto Rico.

    Product
    Gildess 1.5/30 (norethindrone acetate, 1.5 mg and ethinyl estradiol tablets, 0.03 mg, USP), 21 count, (a) 3 blisters (NDC 0603-7606-48) and (b) 6 blisters (NDC 0603-7606-15), Rx only, Manufactured in Canada By: Patheon, Inc., Ontario, Canada L5N 7K9, Manufactured for QUALITEST…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0331-2017·2016-11-09

    Arrow Hands-Off Infusion Port Thermodilution Catheter Recalled for Labeling Inconsistency

    Arrow International Inc is recalling specific lots of Hands-Off Infusion Port Thermodilution Catheters due to a labeling inconsistency. The recall covers 330 units in the US and 1,031 units outside the US.

    Product
    HANDS-OFF Infusion Port Thermodilution Catheter consists of the Arrow IPTD thermodilution catheter enclosed in a contamination shield (Arrow Cath-Gard) with integral flushing/balloon test chamber, enabling the practitioner to prepare, test, and insert the catheter without…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0120-2017·2016-11-09

    Par Pharmaceutical Recalls Subpotent Gildess 1/20 Oral Contraceptive Tablets

    Par Pharmaceutical is recalling Gildess 1/20 tablets because they contain subpotent levels of ethinyl estradiol. The recall covers 393,981 tablets distributed nationwide and in Puerto Rico.

    Product
    Gildess 1/20 (norethindrone acetate, 1 mg and ethinyl estradiol tablets, 0,02 mg, USP), 21 count, (a) 3 blisters (NDC 0603-7607-48) and (b) 6 blisters (NDC 0603-7607-15), Rx only, Manufactured in Canada By: Patheon, Inc., Ontario, Canada L5N 7K9, Manufactured for QUALITEST…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0123-2017·2016-11-09

    Par Pharmaceutical Recalls Subpotent Gildess 24 FE 1.5/30 Oral Contraceptives

    Par Pharmaceutical is recalling Gildess 24 FE 1.5/30 oral contraceptives because the ethinyl estradiol component is subpotent. The recall covers 44,127 tablets distributed nationwide and in Puerto Rico.

    Product
    Gildess 24 FE 1.5/30 (norethindrone acetate, 1 mg and ethinyl estradiol tablets, 0.02 mg, USP and ferrous fumarate tablets, USP 75 mg), 28 count, (a) 3 blisters (NDC 0603-7610-49), and (b) 6 blisters (NDC 0603-7610-17), Rx only, Manufactured in Canada By: Patheon, Inc.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0121-2017·2016-11-09

    Par Pharmaceutical Recalls Subpotent Gildess FE 1/20 Oral Contraceptive Tablets

    Par Pharmaceutical is recalling Gildess FE 1/20 tablets because the ethinyl estradiol component is subpotent. The recall covers 822,009 tablets distributed nationwide and in Puerto Rico.

    Product
    Gildess FE 1/20 (norethindrone acetate, 1 mg and ethinyl estradiol tablets, 0.02 mg, USP and ferrous fumarate tablets, USP 75 mg), 28 count, 6 blisters (NDC 0603-7609-17), Rx only, Manufactured in Canada By: Patheon, Inc., Ontario, Canada L5N 7K9, Manufactured for QUALITEST…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0118-2017·2016-11-09

    Actavis Recalls Ramipril Capsules Due to Incorrect Expiration Date Labeling

    Actavis is recalling 15,984 bottles of Ramipril Capsules because they were labeled with an incorrect expiration date of 03/18 instead of 09/17.

    Product
    Ramipril Capsules, USP, 1.25 mg, 30-count bottle, Rx only, Manufactured by: Arrow Pharm (Malta) Ltd., Birzebbugia, BBG3000, Malta; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054, NDC 16252-570-30.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0122-2017·2016-11-09

    Par Pharmaceutical Recalls Subpotent Gildess FE 1.5/30 Oral Contraceptive Tablets

    Par Pharmaceutical is recalling Gildess FE 1.5/30 tablets because they may contain subpotent levels of ethinyl estradiol.

    Product
    Gildess FE 1.5/30 (norethindrone acetate, 1.5 mg and ethinyl estradiol tablets, 0.03 mg, USP and ferrous fumarate tablets, USP 75 mg), 6 blisters (28 count), NDC 0603-7608-17, Rx only, Manufactured in Canada By: Patheon, Inc., Ontario, Canada L5N 7K9, Manufactured for QUALITEST…
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·105-2016·2016-11-08

    Water Lilies Food Recalls Egg Rolls Due to Undeclared Shrimp Allergen

    Water Lilies Food Inc. is recalling approximately 1,710 pounds of egg rolls because they contain undeclared shrimp and are mislabeled as pork.

    Product
    Water Lilies Food, LLC — Water Lilies Food Inc. Recalls Egg Roll Product Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V810000·2016-11-08

    Newmar Recalls 2017 Motorhomes Due to Throttle Circuit Wire Interference

    Newmar is recalling 51 model year 2017 motorhomes because throttle circuit wires may not be twisted, potentially causing unintended acceleration or deceleration.

    Product
    NEWMAR — NEWMAR LONDON AIRE, MOUNTAIN AIRE, KING AIRE, ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V812000·2016-11-08

    Hyundai Translead Recalls 2012-2013 HT Trailers Due to Cracking I-Beams

    Hyundai Translead is recalling 892 model year 2012-2013 HT trailers because I-beams may crack, potentially causing the bogie to detach and increasing crash risk.

    Product
    HYUNDAI TRANSLEAD — HYUNDAI TRANSLEAD HT HYCUBE, HT ORIGINAL, HT COMPOSITE-XT, HT COMPOSITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17709·2016-11-08

    Trane Recalls Furnaces Due to Electrical Shock Hazard

    Trane is recalling about 17,700 furnaces because a loose ground wire creates a shock hazard if an electrical component fails.

    Product
    Furnaces
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V813000·2016-11-08

    Chrysler Recalls 2016 Dodge Dart for Windshield Wiper Circuit Failure

    Chrysler is recalling 53,155 2016 Dodge Dart vehicles because a faulty washer pump can cause the wiper circuit to fail, reducing visibility and increasing crash risk.

    Product
    DODGE — DODGE DART
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V809000·2016-11-07

    Daimler Trucks Recalls 2016-2017 FCCC Chassis for Fire Risk

    Daimler Trucks is recalling 1,827 model year 2016-2017 FCCC recreational vehicle chassis because an incorrectly routed power steering hose may cause electrical arcing and a fire.

    Product
    FCCC — FCCC XCR, XCM, XCL, XBR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V806000·2016-11-07

    Terex Advance Front Discharge Concrete Mixers Recalled for Axle Defect

    Terex Advance is recalling 2016-2017 Front Discharge Concrete Mixers because a front axle king-pin may fracture, potentially causing wheel separation and loss of vehicle control.

    Product
    TEREX ADVANCE — TEREX ADVANCE FRONT DISCHARGE CONCRETE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V802000·2016-11-04

    GM Recalls 2017 Cadillac XT5 and GMC Acadia for Brake Caliper Defect

    General Motors is recalling 2017 Cadillac XT5 and GMC Acadia vehicles because front brake caliper seals may leak fluid, reducing braking performance.

    Product
    CADILLAC — CADILLAC, GMC XT5, ACADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide