The Recall Desk

State

Northern Mariana Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

55001–55025 of 73850

  • HighFDA (Devices)·Z-1262-2015·2015-03-18

    Medela Recalls Sterile Enteral Feeding Syringes Due to Packaging Breach

    Medela Inc. is recalling sterile enteral feeding syringes because a potential packaging breach may have compromised their sterility.

    Product
    - NTL-30 30ml Nutrio Enteral Feeding Syringe (sterile) - NTL-60 60ml Nutrio Enteral Feeding Syringe (sterile) - TL-INT-60 60ml Nutrio Enteral Feeding Syringe with Twistlok adapter (sterile) - INT-60 60mL Nutrio Intopo Enteral Feeding Syringe (sterile) - NGF-60 60ml Nutrio…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1259-2015·2015-03-18

    Arrow Intra-Aortic Balloon Catheter Kit Recalled for Potential Helium Leak

    Arrow International Inc is recalling 166 units of Intra-Aortic Balloon Catheter Kits due to a potential leak that allows helium to escape.

    Product
    Arrow Intra-Aortic Balloon Catheter Kit Fiberoptix (IAB), 8 Fr 40 cc Model: IAB-05840-LWS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·15C001000·2015-03-18

    Graco Recalls Child Seats Due to Missing Instruction Manual Label

    Graco is recalling specific child seats manufactured in 2014-2015 because they lack a label indicating where to find the instruction manual, potentially leading to improper use.

    Product
    CHILD SEAT recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1252-2015·2015-03-18

    Siemens RAPIDPoint 405 Blood Gas Analyzer Recalled for Neonatal Bilirubin Variability

    Siemens is recalling 3,420 RAPIDPoint 405 Blood Gas Analyzers worldwide because the neonatal bilirubin parameter may show increased variability under specific high-concentration conditions.

    Product
    RAPIDPoint 405 Blood Gas Analyzer; Siemens Material Number: 10310464, 10322347, 10314817, 10317193, 10318999, 10320055, 10322347, 10328278, 10328302, 10336784. These systems are intended for near-patient and laboratory testing of blood gases, electrolytes, metabolites, total…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0408-2015·2015-03-18

    Micro Labs Recalls Simvastatin Tablets Due to Impurity Failure

    Micro Labs USA Inc. is recalling Simvastatin Tablets, 40mg, because the product failed a known impurity specification. The recall affects 13,488 bottles distributed nationwide.

    Product
    Simvastatin Tablets, USP, 40mg, Rx Only, 90 count bottles, Manufactured by: Micro Labs Limited Goa-403 722, India, Manufactured for: Micro Labs USA Inc., Princeton, NJ 08540 NDC 42571-0040-90.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1265-2015·2015-03-18

    Southern Implants Recalls Dental Implants Due to Labeling Mismatch

    Southern Implants, Inc. is recalling 130 units of MAX-TL and Z-MAX dental implants because the labeled packages contained the wrong implant type.

    Product
    MAX-TL 9.0 x 7.0 mm Implant, Catalog No. 15711K; Z-MAX Implant 9.0 x 7 mm Length, Catalog No. Z-MAX9-7. Dental implant. Product Usage: The MAX Implant is intended to be implanted in the upper and lower jaw arches to provide support for fixed or removable dental prostheses…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0409-2015·2015-03-18

    Micro Labs Recalls Simvastatin Tablets Due to Impurity Failure

    Micro Labs USA Inc. is recalling 13,464 bottles of Simvastatin 80mg tablets because the product failed a known impurity specification.

    Product
    Simvastatin Tablets, USP, 80mg, Rx Only, 90 count bottles, Manufactured by: Micro Labs Limited Goa-403 722, India, Manufactured for: Micro Labs USA Inc., Princeton, NJ 08540 NDC 42571-080-90.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1255-2015·2015-03-18

    Siemens RAPIDLab 1265 System Recalled for Neonatal Bilirubin Variability

    Siemens Healthcare Diagnostics Inc is recalling 2,863 RAPIDLab 1265 Systems because the neonatal bilirubin parameter may show increased variability under specific high-concentration conditions.

    Product
    RAPIDLab 1265 System; Siemens Material Number: 10491395, 10321852, 10335524. The Rapidlab 1200 systems are intended for in vitro diagnostic use by healthcare professionals in the quantitative testing of human whole blood. The systems can determine the following parameters…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1253-2015·2015-03-18

    Siemens RAPIDPoint 500 Blood Gas Analyzer Recalled for Neonatal Bilirubin Variability

    Siemens is recalling 4,376 RAPIDPoint 500 Blood Gas Analyzers worldwide because the neonatal bilirubin parameter may show increased variability under specific high-concentration conditions.

    Product
    RAPIDPoint 500 Blood Gas Analyzer; Siemens Material Number: 10492730, 10696855, 10696857, 10697306. The RAPIDPoint 500 system is designed for professional use in a point-of-care or laboratory environment. This system tests blood gases, electrolytes, metabolites, total…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0411-2015·2015-03-18

    Qualitest Recalls Promethazine DM Syrup Due to Plastic Particulates

    Qualitest Pharmaceuticals is recalling 972 bottles of Promethazine DM Syrup because plastic cap closure particulates may be present in the product.

    Product
    PROMETHAZINE DM SYRUP (Promethazine Hydrochloride, USP and Dextromethorphan Hydrobromide, USP), EACH 5 ml (ONE TEASPOONFUL) CONTAINS: Promethazine Hydrochloride 6.25 mg, Dextromethorphan Hydrobromide 15 mg, alcohol 7%, ONE PINT (574 mL), Rx only, Manufactured for: QUALITEST…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1254-2015·2015-03-18

    Siemens RapidLab 1245 System Recalled for Neonatal Bilirubin Variability

    Siemens is recalling 241 RapidLab 1245 systems because the neonatal bilirubin parameter may show increased variability under specific high-concentration conditions.

    Product
    RAPIDLab 1245 System; Siemens Material Number: 10321844, 10491393, 10337179. The Rapidlab 1200 systems are intended for in vitro diagnostic use by healthcare professionals in the quantitative testing of human whole blood. The systems can determine the following parameters…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1263-2015·2015-03-18

    Ortho-Clinical VITROS Hand-held Barcode Scanner Recall for Sample Skipping

    Ortho-Clinical Diagnostics is recalling VITROS Hand-held Barcode Scanners because they may skip sample cup positions when using the Batch Programming option.

    Product
    VITROS Hand-held Barcode Scanner, Catalog Number 6844210, for use with the following VITROS Systems: VITROS 5,1 FS Chemistry System, VITROS 3600 Immunodiagnostics System, VITROS 4600 Chemistry System, VITROS 5600 Integrated System. This product is an accessory for use with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0407-2015·2015-03-18

    Micro Labs Recalls Simvastatin Tablets Due to Impurity Failure

    Micro Labs USA Inc. is recalling specific lots of Simvastatin Tablets, 20mg, because the product failed a known impurity specification.

    Product
    Simvastatin Tablets, USP, 20mg a) 90- count bottle (42517-0020-10), b) 1000-count-bottle (NDC 42571-0020-10), Rx only, Manufactured by: Micro Labs Limited Goa-403 722, India, Manufactured for: Micro Labs USA Inc.,Princeton, NJ 08540
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V154000·2015-03-17

    Hyundai Translead Recalls 2014-2015 Trailers Due to Brake Drag Risk

    Hyundai Translead is recalling 3,412 model year 2014-2015 trailers because improperly seated brake diaphragms may cause drag, potentially leading to wheel end fires.

    Product
    HYUNDAI TRANSLEAD — HYUNDAI TRANSLEAD CONVERTER DOLLY TRAILER, VAN TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V152000·2015-03-16

    Ducati Recalls Multistrada 1200 Motorcycles Due to Throttle Cable Defect

    Ducati is recalling 2010-2014 Multistrada 1200 motorcycles because a moving throttle cable sleeve may prevent the throttle from closing fully, increasing crash risk.

    Product
    DUCATI — DUCATI MULTISTRADA 1200
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V151000·2015-03-16

    Spartan Tool Sewer Jetter Trailer Hitch Weld Failure Recall

    Spartan Tool is recalling 2013-2014 Sewer Jetters because trailer hitch welds may fail, causing the trailer to detach from the tow vehicle.

    Product
    SPARTAN TOOL — SPARTAN TOOL SEWER JETTER 740, SEWER JETTER 758, SEWER JETTER 738
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V150000·2015-03-16

    Altec Recalls 2014 Aerial Devices Due to Counterbalance Valve Defect

    Altec is recalling 2014 Aerial Devices because a counterbalance valve may crack, causing hydraulic leaks and unintended boom movement that increases injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V149000·2015-03-16

    Newmar Recalls 2014-2015 Motor Homes Due to Wiper Blade Separation Risk

    Newmar is recalling 153 model year 2014-2015 motor homes because wiper blades may separate from the arms, reducing driver visibility and increasing crash risk.

    Product
    NEWMAR — NEWMAR ESSEX, LONDON AIRE, MOUNTAIN AIRE, KING AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V147000·2015-03-13

    BMW Recalls 2014-2015 X5 Models for Air Bag Connection Defect

    BMW is recalling certain 2014-2015 X5 vehicles because the Head Protection System air bag may not be securely connected to the inflator, increasing injury risk in a crash.

    Product
    BMW — BMW X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V146000·2015-03-13

    GM Recalls 2015 Buick Encore and Chevrolet Trax for Steering Defect

    General Motors is recalling 2015 Buick Encore and Chevrolet Trax vehicles because steering column wear may cause sudden loss of power steering assist, increasing crash risk.

    Product
    CHEVROLET — CHEVROLET, BUICK TRAX, ENCORE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V144000·2015-03-13

    Toyota Recalls 2014-2015 Camry, Highlander, and RAV4 for Steering Defect

    Toyota is recalling specific 2014-2015 Camry, Highlander, and RAV4 vehicles because a manufacturing defect in the electric power steering system may cause it to fail, increasing crash risk.

    Product
    TOYOTA — TOYOTA CAMRY, RAV4, HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15V145000·2015-03-13

    GM Recalls 2011-2013 Chevrolet Volt for Carbon Monoxide Risk

    General Motors is recalling 2011-2013 Chevrolet Volt vehicles because the engine may start automatically if the electrical system is left on, posing a carbon monoxide risk in enclosed spaces.

    Product
    CHEVROLET — CHEVROLET VOLT
    Category
    Vehicle
    Distribution
    Distributed nationwide