The Recall Desk

State

Northern Mariana Islands product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53401–53425 of 73847

  • HighFDA (Devices)·Z-1737-2015·2015-06-17

    Smith & Nephew R3 Constrained Liner Recalled for Sizing Defect

    Smith & Nephew is recalling 12 units of R3 Constrained Liners because the locking groove is oversized, which may prevent the locking ring from engaging properly.

    Product
    R3(TM) 22 MM I.D., 58 MM O.D. CONSTRAINED LINER, REF 71339158, QTY: (1), STERILE EO. Product Usage: The R3 Constrained liner Acetabular System is a cemented or uncemented prosthesis intended to replace a hip joint. The Constrained liner is intended for primary or revision…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1778-2015·2015-06-17

    Philips Precedence 16 UPS Accessory Devices Recalled for Battery Acid Leakage

    Philips Medical Systems is recalling 36 Precedence 16 UPS accessory devices used in CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.

    Product
    Precedence 16 (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1776-2015·2015-06-17

    Philips Recalls Gemini 16 PET/CT Uninterruptible Power Supply Accessories

    Philips is recalling 7 Gemini 16 PET/CT Uninterruptible Power Supply units worldwide due to risks of battery acid leakage, overheating, and fumes.

    Product
    Gemini 16 PET/CT System (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2398-2015·2015-06-17

    Reaction Nutrition Recalls Creatine Supplements for Potential Allergen Contamination

    Reaction Nutrition is recalling specific lots of RN BlueChip Creatine Monohydrate because shared equipment use may result in undeclared whey protein and soy.

    Product
    RN BlueChip: Creatine, Creatine Monohydrate, 400 grams, Distributed by Reaction Nutrition, Carnegie, PA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2418-2015·2015-06-17

    Natural Creations Recalls New Zealand Colostrum Supplement Due to Milk Allergen

    Natural Creations is voluntarily recalling 399 bottles of New Zealand Colostrum dietary supplement because it contains an unidentified milk allergen.

    Product
    250cc White Plastic Container containing 120 capsules, labeled Natural Creations New Zealand Colostrum, Colostrum Supplement, MFG. FOR: Natural Creations, Woodbine, IA 51579, 712-647-1600
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1786-2015·2015-06-17

    Philips Recalls GEMINI TF PET/CT 16 Slice UPS Accessory Devices

    Philips is recalling 69 GEMINI TF PET/CT 16 Slice systems due to UPS accessory devices that may leak battery acid, overheat, or emit fumes.

    Product
    GEMINI TF PET/CT 16 Slice (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1728-2015·2015-06-17

    Ortho-Clinical VITROS 5,1 FS Chemistry System Software Recall

    Ortho-Clinical Diagnostics is recalling VITROS 5,1 FS Chemistry System software due to a defect that allows improper sample metering for urine assays requiring acidification.

    Product
    VITROS 5,1 FS Chemistry System, Software Version 2.8 & Below Automates pre-analytical and post-analytical sample and data management for in vitro diagnostic use. VITROS Urine Assays: VITROS Calcium (Ca), Magnesium (Mg), and Phosphorus (Phos) requires acidification…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2397-2015·2015-06-17

    Reaction Nutrition Recalls L-Glutamine Powder for Potential Allergen Contamination

    Reaction Nutrition is recalling L-Glutamine Powder because it may contain undeclared whey protein and soy due to shared equipment use.

    Product
    RN BlueChip: Glutamine, L-Glutamine Powder, 400 grams, Distributed by Reaction Nutrition, Carnegie, PA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2389-2015·2015-06-17

    Reaction Nutrition Recalls Bio Armor Carno Pump Plus Due to Allergen Cross-Contact

    Reaction Nutrition is recalling Bio Armor Carno Pump Plus Electrolytes because shared equipment may cause cross-contact with whey protein and soy.

    Product
    Bio Armor Carno Pump Plus Electrolytes 40 servings (Blue Raspberry), Distributed by Reaction Nutrition, Carnegie, PA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1791-2015·2015-06-17

    Philips Recalls BrightView SPECT UPS Accessory Devices for Safety Hazards

    Philips Medical Systems is recalling 277 BrightView SPECT UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.

    Product
    BrightView SPECT (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1732-2015·2015-06-17

    Edwards Lifesciences Recalls ClearSight Heart Reference Sensor Due to Damage

    Edwards Lifesciences is recalling ClearSight Heart Reference Sensors because the finger component may be damaged. The recall affects 1,309 units distributed worldwide.

    Product
    ClearSight, Model No. EVHRS Heart Reference Sensor. The EV1000 Clinical Platform Nl and ClearSight finger cuffs noninvasively measures blood pressure and associated hemodynamic parameters.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1784-2015·2015-06-17

    Philips CardioMD III UPS Accessory Devices Recalled for Battery Acid Leakage

    Philips Medical Systems is recalling 81 CardioMD III UPS accessory devices for CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.

    Product
    CardioMD III (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1761-2015·2015-06-17

    Philips Recalls CT Scanner UPS Accessories Due to Battery Acid Leakage Risk

    Philips Medical Systems is recalling 788 Uninterruptible Power Supply (UPS) accessories for CT scanners due to risks of battery acid leakage, overheating, and fume emission.

    Product
    Brilliance CT 64 channel with Essence, Technology (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1785-2015·2015-06-17

    Philips Ingenuity TF UPS Accessory Devices Recalled for Battery Acid Leakage

    Philips Medical Systems is recalling 14 Ingenuity TF UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.

    Product
    Ingenuity TF (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1753-2015·2015-06-17

    Gyrus ACMI Diego Elite Tubeset Recalled for Sterility Assurance Concerns

    Gyrus Acmi is recalling 22,250 boxes of Diego Elite Tubesets due to a potential lack of sterility assurance. The devices are used for ENT and head and neck procedures.

    Product
    Gyrus ACMI Diego Elite Tubeset, intended for cutting, coagulation, drilling, debriding, and removal of bone, and soft and hard tissue in general ENT, Sinus/Rhinology, Nasopharyngeal/Laryngology, and Head and Neck procedures. Catalog No. TS101DC, Lot numbers JC924165 and below…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2401-2015·2015-06-17

    Reaction Nutrition Recalls Amino Action Supplements Due to Undeclared Whey Protein

    Reaction Nutrition is recalling Amino Action supplements because they may contain undeclared whey protein due to shared equipment use.

    Product
    REACTION RECOR: Amino Action- 500g (Island Breeze), Distributed by Reaction Nutrition, Carnegie, PA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1759-2015·2015-06-17

    Philips Medical Systems Recalls MX 16 Slice UPS Accessory Devices

    Philips Medical Systems is recalling 125 MX 16 Slice UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.

    Product
    MX 16 Slice (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1789-2015·2015-06-17

    Philips Recalls GEMINI TF Big Bore UPS Accessory Devices for Leakage Risk

    Philips Medical Systems is recalling 39 GEMINI TF Big Bore UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.

    Product
    GEMINI TF Big Bore (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1739-2015·2015-06-17

    Smith & Nephew Recalls R3 Constrained Liner Due to Sizing Defect

    Smith & Nephew is recalling 32 units of R3 Constrained Liners because the locking groove is oversized, which may prevent the locking ring from engaging properly.

    Product
    R3(TM) 28 MM I.D., 62 MM O.D. CONSTRAINED LINER, REF 71339162, QTY: (1), STERILE EO. Product Usage: The R3 Constrained liner Acetabular System is a cemented or uncemented prosthesis intended to replace a hip joint. The Constrained liner is intended for primary or revision…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1743-2015·2015-06-17

    Ortho-Clinical VITROS 5600 Chemistry System Software Recall

    Ortho-Clinical Diagnostics is recalling VITROS 5600 Chemistry Systems due to a software anomaly that may allow multiple assays to be tested on a single urine specimen, potentially leading to biased patient results.

    Product
    VITROS 5600 Chemistry System, Software Version 3.2 & Below. Automates pre-analytical and post-analytical sample and data management for in vitro diagnostic use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1747-2015·2015-06-17

    Becton Dickinson Recalls BBL Port A Cul Tubes Due to Oxidation

    Becton Dickinson is recalling BBL Port A Cul tubes with Swabs Sterile Pack because excessive oxidation may affect the viability of anaerobic microorganisms.

    Product
    BBL Port A Cul tubes with Swabs Sterile Pack, catalog number 221607. For patient sample collection.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1769-2015·2015-06-17

    Philips iCT SP UPS Accessory Devices Recalled for Battery Acid Leakage Risk

    Philips Medical Systems is recalling 110 iCT SP UPS accessory devices used with CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.

    Product
    iCT SP (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2391-2015·2015-06-17

    Reaction Nutrition Recalls Bio Armor CreaMatrix for Undeclared Allergens

    Reaction Nutrition is recalling Bio Armor CreaMatrix supplements because they may contain undeclared whey protein and soy.

    Product
    Bio Armor CreaMatrix 306g 60 servings Unflavored, Distributed by Reaction Nutrition, Carnegie, PA
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1735-2015·2015-06-17

    Smith & Nephew Recalls R3 Constrained Liner Due to Sizing Defect

    Smith & Nephew is recalling 17 units of the R3 Constrained Liner because the locking groove is oversized, potentially preventing the locking ring from engaging.

    Product
    R3(TM) 22 MM I.D., 52 MM O.D. CONSTRAINED LINER, REF 71339152, QTY: (1), STERILE EO. Product Usage: The R3 Constrained liner Acetabular System is a cemented or uncemented prosthesis intended to replace a hip joint. The Constrained liner is intended for primary or revision…
    Category
    Medical Device
    Distribution
    Distributed nationwide