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.

58301–58325 of 73856

  • ModerateFDA (Devices)·Z-1610-2014·2014-05-21

    Ortho Development Recalls PS-C Femoral Knee Implant Components

    Ortho Development Corporation is recalling five PS-C Femoral Nonporous Rt Sz 6 knee implant components because pegged versions were found in boxes labeled for the pegless version.

    Product
    PS-C Femoral Nonporous Rt Sz 6, Model Number 161-1604 Component of the Balanced Knee System and Balanced Knee Revision System, for total knee arthroplasty procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1611-2014·2014-05-21

    Mindray DPM 6 Patient Monitor Recalled for Uncleared ST/Arrhythmia Feature

    Mindray DS USA is recalling four DPM 6 patient monitors in Ohio because the included Multi Parameter Module contains a cardiac ST/Arrhythmia analysis feature that is not cleared for marketing.

    Product
    DPM 6 Monitor in use with a Multi Parameter Module (MPM). Patient monitor used for monitoring, displaying, reviewing, storing, and alarming of multiple physiological parameters including ECG, arrhythmia detection, ST segment analysis, heart rate (HR), respiration rate (RESP)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1614-2014·2014-05-21

    Greatbatch Recalls Coaxial Micro-Introducer Kits Due to Shelf Life Documentation Issues

    Greatbatch Medical is recalling Coaxial Micro-Introducer Kits because documentation does not support the claimed five-year shelf life.

    Product
    Coaxial Micro-Introducer Kit. Greatbatch Part Number/Bard Access Systems Order Number/Part Description 10636-001 8004011 Kit Coax 10 Pack 4FR Bard 10636-002 8005011 Kit Coax 10 Pack 5FR Bard 10636-007 8004012 Kit Coax 10 Pack 4FR Bard 10636-008 8005012 Kit…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1574-2014·2014-05-21

    Anspach Cutting Bur Recall Due to Incorrect Product Code Labeling

    The Anspach Effort, Inc. is recalling 30 Anspach Cutting Burs (REF L-3SD) because the product code S-3SD was included, which is shorter than the labeled product.

    Product
    ANSPACH Cutting bur, 3 mm Diamond Ball, Standard Length. REF L-3SD Use with LONG Attachments. Used for cutting and shaping bone, including the spine and cranium.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1323-2014·2014-05-21

    First Aid Only Recalls Ibuprofen Dispenser Boxes Containing Aspirin

    First Aid Only is recalling Smart Tab First Aid ezRefill System Ibuprofen boxes that were accidentally filled with aspirin packs.

    Product
    Smart Tab First Aid ezRefill System Ibuprofen dispenser boxes (Item Number FAE 7014), 20 count boxes, First Aid Only Inc., Vancouver, WA
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1316-2014·2014-05-21

    Flawless Beauty LLC Recalls Laroscorbine Platinium Injectable Solution

    Flawless Beauty LLC is recalling Laroscorbine Platinium injectable solution because it was marketed without an approved NDA/ANDA and includes drug claims to act as an antidote.

    Product
    Laroscorbine Platinium (vitamin C/collagen) injectable I.V. solution, 1 gm/0.35 gm, 5 mL ampoules, packaged in 10-count ampoules per box, Laboratories Roche Nicholas S.A., F-74240 Gaillard, - Tel.: 04 50 87 70 70, Fabricant : Produits Roche, 52, Bld du Parc, 92521 Neulilly…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1617-2014·2014-05-21

    McKesson Radiology-PACS software recall for missing high-priority alert icon

    McKesson Medical Imaging is recalling 45 units of McKesson Radiology-PACS software because the high-priority alert icon was not displayed when no Stat studies were present.

    Product
    McKesson Radiology-PACS. McKesson Radiology is a medical image and information application that is intended to receive, transmit, store, retrieve, display, print and process digital medical images, digital medical video, and associated medical information from various medical…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1294-2014·2014-05-21

    Teva Recalls Indomethacin Capsules Due to Manufacturing Quality Deviations

    Teva Pharmaceuticals USA is recalling 7,694 bottles of Indomethacin Capsules USP, 25 mg, due to CGMP deviations and laboratory testing failures.

    Product
    INDOMETHACIN Capsules USP, 25 mg 100 count bottle, Rx only , Manufactured In INDIA By: EMCURE PHARMACEUTICALS LTD harmaceuticals Ltd., Hinjwadi, Pune, India, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960, NDC 0093-4029-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1295-2014·2014-05-21

    Teva Recalls Indomethacin Capsules Due to Manufacturing Quality Deviations

    Teva Pharmaceuticals USA is recalling Indomethacin Capsules USP, 50 mg, because laboratory testing was not conducted in accordance with Good Manufacturing Practice (GMP) requirements.

    Product
    INDOMETHACIN Capsules USP, 50 mg, a) 100 count bottle, (NDC 0093-4030-01), b) 500 count bottle, (NDC 0093-4030-05), Manufactured In INDIA By: EMCURE PHARMACEUTICALS LTD harmaceuticals Ltd., Hinjwadi, Pune, India, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1293-2014·2014-05-21

    Teva Recalls Glyburide and Metformin Tablets Due to GMP Deviations

    Teva Pharmaceuticals USA is recalling specific bottles of Glyburide and Metformin Hydrochloride tablets due to laboratory testing deviations from GMP requirements.

    Product
    GLYBURIDE and METFORMIN HYDROCHLORIDE Tablets USP, 5mg/500mg, 500 count bottle, Manufactured In INDIA By: EMCURE PHARMACEUTICALS LTD harmaceuticals Ltd., Hinjwadi, Pune, India, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960, NDC: 0093-5712-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalCPSC·14185·2014-05-20

    Bed Handles Inc. Recalls Portable Bed Handles Due to Entrapment Deaths

    Bed Handles Inc. is recalling about 113,000 portable bed handles sold without safety retention straps. Three deaths were reported after users became entrapped between the mattress and the shifting handles.

    Product
    Portable bed handles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V265000·2014-05-20

    GM Recalls 2015 Silverado HD and Sierra HD for Fire Risk

    General Motors is recalling 2015 Chevrolet Silverado HD and GMC Sierra HD trucks because loose fuse block clips can cause a short circuit and engine compartment fire.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO HD, SIERRA HD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V267000·2014-05-20

    Thor Motor Coach Recalls Outlaw 29H Motorcoaches Due to Fire Risk

    Thor Motor Coach is recalling 2014-2015 Outlaw 29H motorcoaches because the generator exhaust is too close to the propane tank and may release carbon monoxide.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH OUTLAW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V266000·2014-05-20

    GM Recalls 2009-2014 SUVs for Seatbelt Cable Defect

    General Motors is recalling specific 2009-2014 Buick, Chevrolet, GMC, and Saturn SUVs because a seatbelt cable may separate, increasing injury risk in a crash.

    Product
    BUICK — BUICK, GMC, SATURN ENCLAVE, ACADIA, OUTLOOK, TRAVERSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·030-2014·2014-05-19

    Wolverine Packing Recalls Ground Beef Due To Possible E. Coli O157:H7

    Wolverine Packing Company is recalling approximately 1.8 million pounds of ground beef products due to possible E. coli O157:H7 contamination.

    Product
    Wolverine Packing Co. — Michigan Firm Recalls Ground Beef Products Due To Possible E. Coli O157:H7
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E026000·2014-05-19

    Agility Fuel Systems Recalls CNG Tank Rail Mount Systems

    Agility Fuel Systems is recalling CNG Tank Rail Mount Systems manufactured between September 2010 and January 2013. The defect may allow the tank to move, potentially damaging fuel lines and increasing fire risk.

    Product
    FUEL SYSTEM, OTHER:STORAGE:TANK ASSEMBLY:MOUNTING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V262000·2014-05-19

    Suzuki Recalls Forenza and Reno Vehicles for Headlamp Fire Risk

    Suzuki is recalling 2004-2008 Forenza and 2005-2008 Reno vehicles because heat in the headlamp switch or DRL module could melt components and cause a fire.

    Product
    SUZUKI — SUZUKI FORENZA, RENO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14E025000·2014-05-19

    Agility Fuel Systems Recalls CNG Fuel Tank Systems for Valve Defect

    Agility Fuel Systems is recalling CNG Fuel Tank Systems where the manual shutoff valve may get stuck closed, posing a safety risk to service personnel.

    Product
    FUEL SYSTEM, OTHER:STORAGE:TANK ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·028-2014·2014-05-16

    Transatlantic Foods Recalls Pork and Poultry Products Due to Lack of Inspection

    Transatlantic Foods is recalling approximately 222,000 pounds of pork and poultry products because they were produced without the required USDA inspection.

    Product
    New York Firm Recalls Pork and Poultry Products Due To Lack of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V258000·2014-05-16

    Honda Recalls 2013 Fit Vehicles for Driveshaft Breakage Risk

    Honda is recalling 2013 Fit vehicles with manual transmissions because the passenger side driveshaft may break, potentially causing loss of power or unexpected movement.

    Product
    HONDA — HONDA FIT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V259000·2014-05-16

    GM Recalls 2015 Cadillac Escalade Models for Air Bag Defect

    General Motors is recalling 2,838 2015 Cadillac Escalade and Escalade ESV vehicles because the front passenger air bag may only partially deploy in a crash.

    Product
    CADILLAC — CADILLAC ESCALADE, ESCALADE ESV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14E023000·2014-05-16

    Harley-Davidson Recalls 2014 XL Sportster Brake Lever Kits

    Harley-Davidson is recalling accessory brake lever kits for 2014 XL Sportster motorcycles because excess chrome plating may prevent the front brake from releasing, increasing crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON XL SPORTSTER
    Category
    Vehicle
    Distribution
    Distributed nationwide