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.

58951–58975 of 73856

  • HighCPSC·14132·2014-03-19

    Vera Bradley Recalls Bear Rattles and Bunny Toys for Choking Hazard

    Vera Bradley is recalling about 98,000 Bear Ring Rattles and Bunny stuffed toys because the pom-pom tail can detach, posing a choking hazard to young children.

    Product
    Vera Bradley Bear Ring Rattles and Bunny Stuffed Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1206-2014·2014-03-19

    DePuy S-ROM Rotating Hinge Femoral Components Recalled for Sterile Barrier Defects

    DePuy Orthopaedics is recalling S-ROM Noiles Rotating Hinge Femoral components due to potential holes in the sterile barrier pouches.

    Product
    REF 623411 R S-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented (with Pin), Right, Small, Sterile R Qty 1 The S-ROM Hinged knee femoral component is used in revision surgeries when there is significant bone loss or ligament instability and additional support is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1195-2014·2014-03-19

    Veridex Recalls CELLTRACKS Analyzer II Microscopes Due to Camera Failures

    Veridex, LLC is recalling 19 CELLTRACKS Analyzer II fluorescence microscopes because of reported camera failures. The devices are used for analyzing rare cells in biological fluids.

    Product
    CELLTRACKS ANALYZER II¿ (Product Code 9555) Product Usage: The CELLTRACKS ANALYZER II¿ is a semi-automated fluorescence microscope, consisting of the analyzer, a dedicated computer with CELLTRACKS¿ software, monitor, keyboard, mouse and uninterruptible power supply (UPS).…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1154-2014·2014-03-19

    Clarity Medical Systems Recalls RetCam Devices Due to Age Calculation Error

    Clarity Medical Systems is recalling RetCam 3, Portable, and Shuttle devices because a software error causes incorrect patient age calculations.

    Product
    RetCam 3, RetCam Portable and RetCam Shuttle; manufactured by Clarity Medical Systems, Inc.; Pleasanton, CA 94588. General ophthalmic imaging including retinal, corneal and external imaging.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1156-2014·2014-03-19

    Mindray Recalls Panorama Central Station for Time Clock Data Lag

    Mindray is recalling 732 Panorama Central Stations because Full Disclosure data and event indicators may lag behind the system time clock.

    Product
    Panaroma Central Station Product Usage: This device can view real time, store, print, graph, and trend patient clinical and demographic data. The device can also set independent alarm limits for data send by the bedside monitor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1634-2014·2014-03-19

    Valued Naturals Natural Coconut Recalled for Sulfite Content

    International Foodsource, LLC is recalling Valued Naturals Natural Coconut because laboratory analysis found 28.1 ppm sulfites.

    Product
    Valued Naturals Natural Coconut Net wt. 8oz (216.80g) Imported by Philippines International Foodsource LLC 52 Richboynton Rd, Dover, NJ 07801 Packaged in 8 oz bag 12 per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1203-2014·2014-03-19

    DePuy S-ROM Rotating Hinge Recall Due to Sterile Barrier Defect

    DePuy Orthopaedics is recalling S-ROM Noiles Rotating Hinge Femur devices because holes may develop in the sterile barrier pouches.

    Product
    REF 623401 L S-ROM Noiles Rotating Hinge, Femoral Rotating Hinge Cemented (with Pin), Left, medium, Sterile R Qty 1 The S-ROM Hinged knee femoral component is used in revision surgeries when there is significant bone loss or ligament instability and additional support is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateNHTSA·14V129000·2014-03-19

    Infiniti Recalls 2014 QX80 Vehicles for Incorrect Certification Label

    Nissan is recalling 2014 Infiniti QX80 vehicles because the certification label lists an incorrect Gross Axle Weight Rating, potentially allowing vehicle overload.

    Product
    INFINITI — INFINITI QX80
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1152-2014·2014-03-19

    Fougera Recalls Triamcinolone Acetonide Cream Due to Labeling Error

    Fougera Pharmaceuticals is recalling 493,192 tubes of Triamcinolone Acetonide Cream 0.1% because the end flap incorrectly displays 01% instead of 0.1%.

    Product
    TRIAMCINOLONE ACETONIDE — TRIAMCINOLONE ACETONIDE (TRIAMCINOLONE ACETONIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1155-2014·2014-03-19

    Mylan Recalls Carisoprodol Tablets Due to Failed Impurity Specification

    Mylan Institutional, Inc. is recalling 3,252 cartons of Carisoprodol Tablets, USP, 350 mg, because the product failed an impurity or degradation specification.

    Product
    Carisoprodol Tablets, USP, 350 mg, unit dose blister packages of 100 tablets (10 cards of 10 tablets each), Rx only, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL NDC 51079-819-20
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1193-2014·2014-03-19

    Ortho-Clinical Diagnostics Recalls VITROS Vitamin D Calibrators for Biased Results

    Ortho-Clinical Diagnostics is recalling VITROS 25-OH Vitamin D Total Calibrators because they may generate negatively biased results. Users must immediately discontinue use of all current lots.

    Product
    VITROS Immunodiagnostic Products 25-OH Vitamin D Total Calibrators; REF/CATALOG # 684 4055, IVD --- COMMON/USUAL NAME: VITROS Vitamin D Calibrators -- Ortho-Clinical Diagnostics High Wycombe HP12 4DP, UK --- For use in the calibration of the VITROS ECi/ECiQ Immunodiagnostic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1166-2014·2014-03-19

    Steris Recalls VERIFY SixCess 270FP Challenge Packs Due to Labeling Error

    Steris is recalling VERIFY SixCess 270FP Challenge Packs because the outer shipping package for one lot incorrectly identifies the lot number.

    Product
    VERIFY¿ SixCess 270FP Challenge Pack, STERIS Corporation, 5960 Heisley Road, Mentor, OH 44060, 440-354-2600. The VERIFY¿ SixCess 270FP Challenge Pack is used to monitor steam sterilization loads processed at 270¿F using typical healthcare dynamic air removal steam…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V127000·2014-03-18

    Thor Motor Coach Recalls 2013-2014 RVs Due to Microwave Fire Risk

    Thor Motor Coach is recalling specific 2013-2014 recreational vehicles because the built-in microwave may start on its own, posing a fire hazard if unattended.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH TUSCANY, CHALLENGER, TUSCANY XTE, PALAZZO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V128000·2014-03-18

    Heartland Recreational Vehicle Recall for Microwave Fire Risk

    Heartland is recalling certain fifth wheel trailers because the installed microwave may start on its own, posing a fire risk if unattended.

    Product
    HEARTLAND — HEARTLAND CYCLONE, LANDMARK, BIGHORN SILVERADO, BIGHORN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14134·2014-03-18

    Schneider Electric Recalls Square D Circuit Breakers Due to Fire Hazard

    Schneider Electric is recalling specific Square D F and K frame circuit breakers because they may fail to trip during overloads, posing fire, burn, and shock risks.

    Product
    Square D branded, molded case F and K frame circuit breakers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V118000·2014-03-17

    GM Recalls 2008-2013 SUVs for Side Air Bag Wiring Defect

    General Motors is recalling specific 2008-2013 Buick, GMC, Chevrolet, and Saturn SUVs because side air bag wiring may prevent deployment in a crash.

    Product
    BUICK — BUICK, GMC, SATURN ENCLAVE, ACADIA, OUTLOOK, TRAVERSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V116000·2014-03-17

    GM Recalls 2013-2014 Cadillac XTS for Brake Booster Fire Risk

    General Motors is recalling 2013-2014 Cadillac XTS vehicles because a dislodged cavity plug may cause corrosion and a resistive short, increasing the risk of a fire.

    Product
    CADILLAC — CADILLAC XTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V125000·2014-03-17

    Volkswagen Recalls 2012-2013 Passat Vehicles for Loose Headlight Bulbs

    Volkswagen is recalling 2012-2013 Passat vehicles because the low beam headlight bulb may become loose and lose electrical contact, potentially reducing visibility.

    Product
    VOLKSWAGEN — VOLKSWAGEN PASSAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V112000·2014-03-14

    Honda Recalls 2005-2010 Odyssey Vehicles for Fuel Pump Leak Risk

    Honda is recalling 2005-2010 Odyssey vehicles because a deteriorating fuel pump strainer cover may leak fuel, increasing the risk of a fire.

    Product
    HONDA — HONDA ODYSSEY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V124000·2014-03-14

    Crane Refuse Vehicles Recalled for Intake Manifold Freeze Risk

    Crane is recalling 2008-2014 refuse vehicles because condensation in the intake manifold may freeze, causing sensor failure and potential fire or burn injury.

    Product
    CRANE — CRANE LE2, LET2, COE, LDT2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14723·2014-03-14

    MobilePower Instant Boost 500 Power Packs Recalled for Fire Hazard

    MobilePower is recalling about 9,800 Instant Boost 500 power packs sold by QVC because they can overheat and cause fires. No injuries have been reported.

    Product
    MobilePower Instant Boost 500 power packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide