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.

59576–59600 of 73856

  • ModerateFDA (Drugs)·D-757-2014·2014-01-29

    Novartis Recalls NeoCitran Extra Strength Powder Packets Due to Foreign Substances

    Novartis Consumer Health is recalling NeoCitran Extra Strength powder packets because they may contain foreign substances. The products were distributed nationwide and internationally.

    Product
    NeoCitran Extra Strength (acetaminophen 650 mg, pseudoephedrine hydrochloride 60 mg, dextromethorphan hydrobromide 20mg, chlorpheniramine maleate 4 mg, ascorbic acid 5 mg) powder packets, Soothing Lemon flavor, 10-single dose pouches per carton, Novartis Consumer Health Canada…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-753-2014·2014-01-29

    Novartis Recalls Theraflu MAX-D Powder Packets Due to Foreign Substances

    Novartis Consumer Health is recalling Theraflu MAX-D and NeoCitran powder packets because they may contain foreign substances.

    Product
    Theraflu MAX-D Severe Cold & Flu (acetaminophen 1000 mg, dextromethorphan HBr 30 mg, guaifenesin 400 mg, pseudoephedrine HCl 60 mg) powder packets, Natural Citrus flavor, 6-count packets per carton, Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0815-2014·2014-01-29

    Bard Access Systems Recalls Low Profile Ports with Undersized Catheters

    Bard Access Systems is recalling Low Profile Ports with 6.6 Fr catheters because some silicone catheters may be undersized to 5.3 Fr.

    Product
    Titanium Single Lumen Low-Profile port, with Pre-Attached open-Ended Silicone 6.6Fr Catheter. Product Code 0602180 Usage: The 6.6 Fr Open-Ended Single-Lumen venous catheters is packaged into various Bard Acess Systems finished goods as Attachable or Preconnected catheters in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0814-2014·2014-01-29

    Bard Access Systems Recalls MRI Low Profile Ports with Undersized Catheters

    Bard Access Systems is recalling MRI Low Profile Single Lumen ports because some silicone catheters may be undersized to 5.3 Fr instead of the labeled 6.6 Fr.

    Product
    MRI Low Profile Single Lumen port with Open-Ended 6.6Fr Silicone Catheter. Product Code 0603880. Product Usage: The 6.6 Fr Open-Ended Single-Lumen venous catheters is packaged into various Bard Acess Systems finished goods as Attachable or Preconnected catheters in BardPort…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0799-2014·2014-01-29

    Zeiss Compensator Slider Lambda 6x20 Recalled for Misalignment

    Carl Zeiss Microscopy is recalling the Compensator Slider Lambda 6x20 component due to misalignment of the lambda plate.

    Product
    Compensator Slider Lambda 6x20 component (part number 473704-0000-000) utilized on all upright ZEISS microscopes (Axio Imager, Axio Scope. A1, Axio Lab. A1). Component used to determine composition of urinary calculi, urinary sediments, bio-crystallates and diagnosis of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-760-2014·2014-01-29

    Novartis Recalls NeoCitran DM Cough and Cold Powder Packets

    Novartis is recalling NeoCitran DM Cough & Cold powder packets because they may contain foreign substances. The products were distributed in the U.S., Canada, and other countries.

    Product
    NeoCitran DM Cough & Cold (dextromethorphan hydrobromide 30 mg, phenylephrine hydrochloride 10 mg, pheniramine maleate 20 mg) powder packets, Natural Source Lemon flavor, 10-count single dose pouches per carton, Novartis Consumer Health Canada, Inc., Mississauga, ON, UPC 0 58478…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0803-2014·2014-01-29

    Civco Belly Board MRI Recalled Due to Misaligned Scales

    Civco Medical Instruments is recalling specific lots of Belly Board MRI devices because scales may be misaligned, potentially affecting measurement accuracy.

    Product
    Civco Belly Board MRI, Reusable non-sterile glass fiber belly board with cushion, REF 126000, packaged 1 per box. Product Usage: This device is intended to reduce the irradiated small bowel volume of gynecological patients undergoing treatment in the pelvic region.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0802-2014·2014-01-29

    Civco Belly Board Recalled Due to Misaligned Scales

    Civco Medical Instruments is recalling 138 belly boards because scales may be misaligned from the zero reference, potentially affecting measurement accuracy.

    Product
    Civco Belly Board, Reusable non-sterile carbon fiber belly board with cushion, REF 125012, packaged 1 per box. Product Usage: This device is intended to reduce the irradiated small bowel volume of gynecological patients undergoing treatment in the pelvic region.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0794-2014·2014-01-29

    Remel Recalls Oxoid Ampicillin Test Discs Due to Missing Antibiotic

    Remel Inc is recalling 80 packs of Oxoid Ampicillin 10 mcg test discs because some cartridges may contain discs not impregnated with antibiotic.

    Product
    Oxoid Antimicrobial Susceptibility Test Discs, Ampicillin 10 mcg., CT0003B, packaged in cartridges of 50 discs, 5 cartridges/pack. The firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England. Used in the semi-quantitative agar diffusion test method for in- vitro…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0819-2014·2014-01-29

    FDA Recalls Composix L/P Mesh Due to Labeling Mismatch

    Davol, Inc. is recalling 19 units of Composix L/P Mesh with Echo PS Positioning System because the product labeling does not match the product configuration.

    Product
    Composix L/P with Echo PS 10" X 13" Product Code 0144113 The Composix L/P Mesh with Echo PS Positioning System is a non-absorbable sterile lightweight mesh prosthesis, with a preattached removable positioning system. This system is indicated and designed for the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0800-2014·2014-01-29

    Siemens ADVIA Chemistry Systems Recalled for Potential Result Misinterpretation

    Siemens is recalling ADVIA 1200 and 1650 chemistry systems because an overflow flag may cause users to misinterpret or edit test results.

    Product
    Siemens ADVIA 1200 and ADVIA 1650 Chemistry Systems. Automated, clinical chemistry analyzers that can run tests on human serum, plasma, or urine.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0811-2014·2014-01-29

    Ziemer FEMTO LDV Z2, Z4, and Z6 Lasers Recalled for Monitor Overheating

    Ziemer USA Inc. is recalling five FEMTO LDV femtosecond surgical lasers because a controller board defect may cause the video monitor to overheat and shut off.

    Product
    1) The FEMTO LDV Z2 Femtosecond Surgical Laser is an ophthalmic surgical laser indicated for use in the creation of corneal incisions in patients undergoing LASIK surgery or other treatment requiring lamellar resection of the cornea at constant depth relative to the corneal…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0801-2014·2014-01-29

    Philips CT Scanner Recall for Obscured Machine Name Label

    Philips is recalling 32 CT scanners because the machine name label is obscured in TumorLOC Basic Mode, preventing users from viewing or changing the name.

    Product
    Computed Tomography X-Ray System (Brilliance CT Big Bore Oncology & Brilliance CT Big Bore Radiology) Distributed by Philips Healthcare System, Cleveland, OH. Produces cross-sectional body images by computer reconstruction of x-ray transmission data taken at different angles…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-747-2014·2014-01-29

    Teva Recalls Fluconazole Oral Suspension for Low Preservative Content

    Teva Pharmaceuticals is recalling Fluconazole Oral Suspension because the product has preservative levels below the required specification.

    Product
    Fluconazole Oral Suspension, 10 mg/mL, 35 ml bottle, RX only, Mfd by Cipla, Ltd., Goa, India, Dist by Teva Pharmaceuticals USA, Inc., Sellersville, PA. NDC: 0093-5414-95.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0821-2014·2014-01-29

    Puritan Bennett Ventilator Manual Addendum Corrected for Oxygen Sensor Life

    Nellcor Puritan Bennett is correcting a labeling error in the PB840 Operator's Manual Addendum that incorrectly stated the oxygen sensor life as two years instead of one.

    Product
    Puritan Bennett 840 Series Ventilator PB840 Operators Manual Addendum PN 066009A 09/02 The intended use of the oxygen sensor is to provide the oxygen concentration of the delivered gas at the patient wye (inspiratory-expiratory interface). The oxygen sensor does not control…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V020000·2014-01-28

    Spartan MM Motorhome Chassis Recalled for Sway Bar End Link Defect

    Spartan Motors is recalling 2010-2014 MM motorhome chassis due to a front suspension design that may cause sway bar end links to break, increasing crash risk.

    Product
    SPARTAN — SPARTAN MM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14091·2014-01-28

    Horizon Hobby Recalls Remote Controlled Model Helicopters Due to Injury Hazard

    Horizon Hobby is recalling specific Blade 500 model helicopters because the tail rotor grip can separate, posing a crash and injury risk.

    Product
    Blade 500 X BNF and Blade 500 3D RTF and BNF Remote Controlled Model Helicopters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V018000·2014-01-27

    Starcraft Transit Buses Recalled for Alternator Harness Pinch Risk

    Starcraft is recalling 2010-2013 transit buses because a pinched alternator harness could cause vehicle stalling or a fire.

    Product
    STARCRAFT — STARCRAFT STARQUEST, XPRESS, ULTRASTAR, STARLITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V021000·2014-01-27

    Trails West RPM Trailers Recalled for Furnace Fire Risk

    Trails West is recalling 2010-2014 RPM trailers due to a furnace defect that may cause melting and fire.

    Product
    TRAILS WEST — TRAILS WEST RPM
    Category
    Vehicle
    Distribution
    Distributed nationwide