The Recall Desk

State

Northern Mariana Islands product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53551–53575 of 73847

  • ModerateFDA (Drugs)·D-1111-2015·2015-06-10

    Mylan Recalls Mycophenolic Acid Tablets for Dissolution Failures

    Mylan Pharmaceuticals is recalling 7,722 bottles of Mycophenolic Acid Delayed-release Tablets, 180 mg, because they failed to meet dissolution specifications.

    Product
    Mycophenolic Acid Delayed-release Tablets, 180 mg, 120-count bottle, Rx only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 U.S.A., NDC 0378-4201-78, UPC 3 0378-4201-78 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1708-2015·2015-06-10

    Siemens Dimension Vista LOCI TSH Test Recalled for Inaccurate Results

    Siemens is recalling 2,256 units of the Dimension Vista LOCI TSH test due to a defect that may cause falsely low results.

    Product
    Dimension Vista Systems LOCI Thyroid Stimulating Hormone; the TSH method is an in vitro diagnostic test for the quantitative measurement of Thyroid Stimulating Hormone in human serum and plasma on the Dimension Vista System.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1705-2015·2015-06-10

    Siemens Medical Software Recall for Missing Image Measurements on Printouts

    Siemens Medical Solutions is recalling 167 units of Syngo.via and Syngo.x software because measurements on subsequent images do not appear on printouts.

    Product
    Syngo.via and Syngo.x ; a software solution intended to be used for viewing, manipulation, communication, and storage of medical images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1112-2015·2015-06-10

    Teva Recalls Zebeta Tablets Due to Failed Dissolution Specifications

    Teva Pharmaceuticals is recalling 889 bottles of Zebeta (bisoprolol fumarate) 10mg tablets because they failed dissolution specifications during stability testing.

    Product
    Zebeta¿ (bisoprolol fumarate), tablets, 10mg, 30-count bottle, Rx only, Manufactured for Teva Pharmaceuticals Inc. 425 Privet Road, Horsham, PA by Duramed Pharmaceuticals, Inc., a subsidiary of Barr Pharmaceuticals, Inc., Pomona, NY 10970 for Teva. NDC 51285-061-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1114-2015·2015-06-10

    Fresenius Kabi Recalls KABIVEN IV Bags Due to Amino Acid Labeling Error

    Fresenius Kabi is recalling 5,488 bags of KABIVEN IV solution because the label lists 3.1% amino acids, but the product actually contains 3.3%.

    Product
    KABIVEN — KABIVEN (DEXTROSE, SOYBEAN OIL, ELECTROLYTES, LYSINE, PHENYLALANINE, LEUCINE, VALINE, THREONINE, METHIONINE, ISOLEUCINE, TRYPTOPHAN, ALANINE, ARGININE, GLYCINE, PROLINE, HISTIDINE, GLUTAMIC ACID, SERINE, ASPARTIC ACID AND TYROSINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1115-2015·2015-06-10

    Sandoz Recalls Cetirizine HCl Chewable Tablets Due to Impurity Failure

    Sandoz, Inc. is recalling specific lots of Cetirizine HCl Chewable Tablets because an impurity exceeded specifications during stability testing.

    Product
    Cetirizine HCl Chewable Tablet, 10 mg, 6-tablets in one blister, in 12 (2 blisters) and 24 (4 blisters) tablet count configurations. Manufactured by Sandoz Private Limited Village-Digham Opp. Thane-Belapur Road Navi Mumbai, 400 078, India, for Sandoz Private Limited 100 College…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1707-2015·2015-06-10

    Ortho-Clinical Diagnostics Recalls VITROS Signal Reagent Due to Labeling Defects

    Ortho-Clinical Diagnostics is recalling VITROS Immunodiagnostic Products Signal Reagent, Lot 3082, because the reagent packs may contain blank labels.

    Product
    VITROS Immunodiagnostic Products Signal Reagent, Product Code 1072693, Unique Device Identifier No. 10758750008360 VITROS Immunodiagnostics Products Signal Reagent (SR) is supplied to users as a sales unit box containing two Signal Reagent Packs. Each Signal Reagent Pack is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V358000·2015-06-09

    GM Recalls 2015 Cadillac ATS and CTS for Brake Pedal Bracket Fracture

    General Motors is recalling 2015 Cadillac ATS and CTS vehicles because a brake pedal bracket may fracture, preventing the driver from applying the brakes.

    Product
    CADILLAC — CADILLAC CTS, ATS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V359000·2015-06-09

    Forest River Recalls 2016 Trailers Due to Wheel Stud Failure Risk

    Forest River is recalling 1,497 model year 2016 trailers because wheel studs may break, potentially causing the wheel to detach and increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER SHOCKWAVE, STEALTH, VIBE, CHEROKEE GREY WOLF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V357000·2015-06-09

    Kalmar Ottawa T2 Tractors Recalled for Engine Fire Risk

    Kalmar is recalling 2010-2014 Ottawa T2 tractors because a vent tube defect may allow engine oil to contact hot surfaces, increasing fire risk.

    Product
    KALMAR — KALMAR OTTAWA T2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V356000·2015-06-09

    Gulf Stream Recalls 2015 Trailers Due to Failing Entry Step Rivets

    Gulf Stream is recalling 2015 Canyon Trail and Sedona trailers because entry step rivets may shear, causing steps to fail and increasing the risk of falls.

    Product
    GULF STREAM — GULF STREAM CANYON TRAIL, SEDONA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V355000·2015-06-09

    Vermeer Recalls 2015 TLR30HD and TLR30LD Trailers for Safety Chain Defect

    Vermeer is recalling specific 2015 TLR30HD and TLR30LD trailers because an incorrectly installed safety chain may fail to prevent the trailer from separating from the tow vehicle.

    Product
    VERMEER — VERMEER TLR30HD, TLR30LD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V351000·2015-06-08

    Mercedes-Benz Recalls 2015 E250, GLK250, and ML250 for Oil Leak Fire Risk

    Mercedes-Benz is recalling specific 2015 E250, GLK250, and ML250 vehicles because oil may leak from the chain tensioner gasket, creating a fire hazard.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E250, GLK250, ML250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V352000·2015-06-08

    Fontaine Recalls 2016 Revolution Trailers Due to Washer Cracking Risk

    Fontaine is recalling 2016 Revolution semi-trailers because hardened washers may crack, potentially causing structural detachment and increasing crash risk.

    Product
    FONTAINE — FONTAINE REVOLUTION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V349000·2015-06-05

    Prevost Recalls 2006-2010 X3-45 Coaches Due to Fire Risk

    Prevost is recalling 314 X3-45 coaches from 2006-2010 because rusted booster studs may break, allowing power cables to short against the frame and cause a fire.

    Product
    PREVOST — PREVOST X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V350000·2015-06-05

    Nova Bus Recalls 2001-2004 LFS Buses for Parking Brake Hose Defect

    Nova Bus is recalling 250 model year 2001-2004 LFS buses because incorrectly connected air hoses may delay parking brake application, increasing crash risk.

    Product
    NOVA BUS — NOVA BUS NOVA LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V348000·2015-06-05

    Prevost Recalls Coaches Due to Fire Suppression Wiring Damage Risk

    Prevost is recalling 452 model year 2010-2014 coaches because engine heat may damage fire suppression wires, potentially causing an engine shutdown and crash.

    Product
    PREVOST — PREVOST H3-45, X3-45, H3-41, XLII-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·087-2015·2015-06-04

    Quincy Street Recalls Pork Sausage Products Due to Foreign Matter Contamination

    Quincy Street, Inc. is recalling approximately 49,308 pounds of pork sausage products that may be contaminated with foreign materials. The products were shipped to institutions nationwide.

    Product
    Quincy Street, Inc. — Quincy Street, Inc. Recalls Pork Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·15159·2015-06-04

    Cree Recalls LED T8 Lamps Due to Overheating and Burn Hazard

    Cree Inc. is recalling approximately 700,000 LED T8 replacement lamps sold in the U.S. because electrical arcing can cause the lamps to overheat and melt, posing a burn hazard.

    Product
    Cree® LED T8 replacement lamps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15158·2015-06-04

    Big Lots Recalls Hanging Chairs Due to Fall Hazard

    Big Lots is recalling about 16,000 hanging chairs because they can tip over and cause falls. Consumers should stop using them and return the base for a refund.

    Product
    Hanging chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1108-2015·2015-06-03

    Hospira Recalls Lactated Ringer's Irrigation Bags Due to Mold Contamination

    Hospira is recalling 24,744 bags of Lactated Ringer's Irrigation due to confirmed mold contamination. The product was distributed nationwide.

    Product
    LACTATED RINGER'S IRRIGATION, USP, 3000 mL flexible container bag, Rx Only, Manufactured by Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7828-08.
    Category
    Medical Device
    Distribution
    Distributed nationwide