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.

57976–58000 of 73856

  • ModerateFDA (Devices)·Z-1801-2014·2014-06-25

    Biomet Recalls EZPass Suture Retriever Due to Nitinol Wire Buckling

    Biomet is recalling 100 units of EZPass Suture Retriever instruments because the nitinol wire may buckle and become kinked, making the device difficult to use.

    Product
    EZPass Suture Retriever, Nitinol, Single Pack, Part number 10007380. Orthopedic Manual Surgical Instrument, Sterile, single use arthroscopic instrument utilized in conjunction with a nitinol wire to aid in passing suture through soft tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1795-2014·2014-06-25

    Boston Scientific Recalls IntellaTip MiFi XP Temperature Ablation Catheters

    Boston Scientific is recalling 968 IntellaTip MiFi XP Temperature Ablation Catheters because some units were not manufactured according to specification.

    Product
    IntellaTip MiFi XP Temperature Ablation Catheter; 8mm x 8F (2.67mm); Large Curve. The BSC Controller and Accessories are indicated for use in conjunction with standard and high power catheters for cardiac ablation procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1802-2014·2014-06-25

    Biomet Recalls EZPass Nylon Monofilament Suture Passers Due to Buckling

    Biomet is recalling 100 units of EZPass Nylon Monofilament Suture Passers because the internal wire may buckle, making the instrument difficult to use.

    Product
    EZPass Nylon Monofilament Single Pack, Part number 110007379, Orthopedic Manual Surgical Instrument Sterile, single use arthroscopic instrument utilized in conjunction with a nitinol wire to aid in passing suture through soft tissue.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1790-2014·2014-06-25

    Roche MODULAR ANALYTICS EVO Serum Work Area Filter Recall

    Roche Diagnostics is recalling 462 Serum Work Area filters for the MODULAR ANALYTICS EVO analyzer due to potential loose components that may cause discrepant results and system alarms.

    Product
    Roche MODULAR ANALYTICS EVO Serum Work Area (SWA), Operator's Manual Software Version 08-02; Filter label: Filter (N) Mat. No 03149773001, Contents 1, 768-320 Filter (N). Product Usage: Fully automated immunoassay analyzer intended for the in-vitro quantitative/qualitative…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1804-2014·2014-06-25

    Ortho-Clinical Diagnostics Recalls VITROS Chemistry Products Calibrator Kit 17

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 17 because calibrator values were assigned using a reference method that was not fully validated.

    Product
    VITROS (R) Chemistry Products Calibrator Kit 17, Product Code/ Catalog Number 6801701 -- For in vitro diagnostic use only --- VITROS Chemistry Products Calibrator Kit 17 is used in conjunction with VITROS Chemistry Products FS Calibrator 1 to calibrate VITROS 5,1 FS Chemistry…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1797-2014·2014-06-25

    Boston Scientific Recalls IntellaTip MiFi XP Temperature Ablation Catheters

    Boston Scientific is recalling IntellaTip MiFi XP Temperature Ablation Catheters because some units were not manufactured according to specification.

    Product
    IntellaTip MiFi XP Temperature Ablation Catheter; 10m x 8F (2.67mm) Standard Curve. The BSC Controller and Accessories are indicated for use in conjunction with standard and high power catheters for cardiac ablation procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1833-2014·2014-06-25

    Synthes External Fixation Systems Recalled for MR Labeling Changes

    Synthes, Inc. is recalling external fixation systems because labeling changes were made to reflect updated protocols for Magnetic Resonance (MR) imaging safety designations.

    Product
    Synthes External Fixation Systems (Small, Medium, Large and DO), bone fixation appliance components.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2031-2014·2014-06-25

    Nutri-West Recalls Total Enzyme and Probiotics Due to Chloramphenicol Risk

    Nutri-West is voluntarily recalling Total Enzyme and Total Probiotics supplements because raw materials may contain Chloramphenicol.

    Product
    Total Enzyme, Dietary Supplement, Nutri-West, 120 capsules, Servicing Size 1 Capsule
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-2036-2014·2014-06-25

    Manischewitz Recalls Tam Tams Snack Crackers Due to Rancidity

    The Manischewitz Company is recalling Tam Tams Snack Crackers Unsalted due to rancidity. The recall covers 29,413 cases distributed nationwide.

    Product
    Tam Tams Snack Crackers Unsalted Net Wt. 9.6 oz (272 g) Distributed by the Manischewitz Company Newark, NJ 07105 Product of USA www.manishewitz.com Packaged in a cardboard box
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-2040-2014·2014-06-25

    Manischewitz Recalls Tam Tams Snack Crackers Due to Rancidity

    The Manischewitz Company is recalling Tam Tams Snack Crackers Original due to rancidity. The recall covers 29,413 units distributed nationwide.

    Product
    Tam Tams Snack Crackers Original Net Wt. 9.6 oz (272 g) Distributed by the Manischewitz Company Newark, NJ 07105 Product of USA www.manishewitz.com Packaged in a cardboard box
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1793-2014·2014-06-25

    Gen-Probe Recalls APTIMA Urine Collection Kits Due to Labeling Error

    Gen-Probe Inc is recalling APTIMA Urine Collection Kits because inner pouches are mislabeled as swab collection kits.

    Product
    APTIMA Urine Collection Kit; Catalog Number 301040, Lots 27231, 27232, 27233, and 27234. Product Usage: The APTIMA Urine Specimen Collection Kit for Male and Female Urine Specimens is for use with APTIMA assays. The APTIMA Urine Specimen Collection Kit is intended to be…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-2037-2014·2014-06-25

    Manischewitz Recalls Tam Tams Snack Crackers Due to Rancidity

    The Manischewitz Company is recalling Tam Tams Snack Crackers in Onion flavor due to rancidity. The recall covers 29,413 units distributed nationwide.

    Product
    Tam Tams Snack Crackers Onion Net Wt. 9.6 oz (272 g) Distributed by the Manischewitz Company Newark, NJ 07105 Product of USA www.manishewitz.com Packaged in a cardboard box
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1387-2014·2014-06-25

    Novartis Recalls Foradil Aerolizer Due to Stability Testing Failures

    Novartis is recalling Foradil Aerolizer inhalation powder capsules because they failed stability specifications for particle size distribution.

    Product
    Foradil Aerolizer (formoterol fumarate inhalation powder), 12 mcg per capsule, 60 Capsules, Rx only, Manufactured for: Merck, Sharpe & Dohne Corp., a subsidiary of Merck & Co., Inc. Whitehouse Station, NJ 08889, Manufactured by: Novartis Pharma AG Basle, Switzerland NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-2038-2014·2014-06-25

    Manischewitz Recalls Tam Tams Snack Crackers Due to Rancidity

    The Manischewitz Company is recalling Tam Tams Snack Crackers Garlic due to rancidity. The recall covers 29,413 units distributed nationwide.

    Product
    Tam Tams Snack Crackers Garlic Net Wt. 9.6 oz (272 g) Distributed by the Manischewitz Company Newark, NJ 07105 Product of USA www.manishewitz.com Packaged in a cardboard box
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-2039-2014·2014-06-25

    Manischewitz Recalls Tam Tams Snack Crackers Due to Rancidity

    The Manischewitz Company is recalling Tam Tams Snack Crackers because of rancidity. The recall affects 29,413 units distributed nationwide.

    Product
    Tam Tams Snack Crackers Everything Net Wt. 9.6 oz (272 g) Distributed by the Manischewitz Company Newark, NJ 07105 Product of USA www.manishewitz.com Packaged in a cardboard box
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V363000·2014-06-24

    Suzuki Recalls 2004-2006 Verona Vehicles Due to Fire Risk

    Suzuki is recalling 2004-2006 Verona vehicles because heat in the daytime running light module could melt and cause a vehicle fire.

    Product
    SUZUKI — SUZUKI VERONA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V364000·2014-06-24

    Vespa 946 Scooters Recalled for Fuel Line Leak Risk

    Piaggio is recalling 2013 Vespa 946 scooters because a fuel line may leak, potentially causing stalling or fire.

    Product
    VESPA — VESPA 946
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14737·2014-06-24

    Trane and American Standard Air Conditioners Recalled for Shock Hazard

    Trane recalls about 100,600 air conditioning units because defective ground screws may not provide sufficient grounding, posing a shock hazard.

    Product
    Trane XB300 and American Standard Silver SI Air Conditioning Systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V358000·2014-06-23

    Gillig Recalls Low Floor Transit Buses Due to Oil Hose Fire Risk

    Gillig is recalling 2007-2014 Low Floor transit buses because an oil sampling hose may leak near hot exhaust components, increasing the risk of fire.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V355000·2014-06-23

    GM Recalls Vehicles for Ignition Switch Airbag Deployment Risk

    General Motors is recalling specific Buick, Cadillac, and Chevrolet models because the ignition switch may move out of the run position, potentially preventing airbag deployment and causing loss of power steering and braking.

    Product
    CADILLAC — CADILLAC, BUICK, CHEVROLET DEVILLE, LACROSSE, MONTE CARLO, DTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V360000·2014-06-23

    Palfleet Recalls 2009-2013 Ford Super Duty Trucks Due to Fire Risk

    Palfleet is recalling 2009-2013 Ford F-350, F-450, and F-550 Super Duty trucks modified with specific PTO assemblies because oil leaks may cause a fire.

    Product
    FORD — FORD F-450 SD, F-550 SD, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide