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.

55601–55625 of 73850

SevereFDA (Devices)·Z-0586-2015·2014-12-31
Heart Sync Multi-function Defibrillation Electrodes Recalled for Incompatibility
Heart Sync, Inc. is recalling multi-function defibrillation electrodes that do not connect with Philips FR3 or FRx AED units, potentially preventing proper use.
Product
ADULT Radiotranslucent Electrode, Part number T100-PHILIPS, Rx ONLY, For use with Philips HeartStart AED "Comparable to Philips Medical HeartStart Electrodes Plug Style Connector", Intended for use during defibrillation, cardioversion, pacing, and ECG monitoring, Single use.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0802-2015·2014-12-31
GE Healthcare Pediatric Defibrillation Electrodes Recalled for Arcing Risk
Leonhard Lang GmbH is recalling GE Healthcare Pediatric Defibrillation Electrodes because arcing may cause malfunction, delaying or preventing life-saving therapy.
Product
GE Healthcare Pediatric Direct-Wired Disposable Defibrillation/Pacing Electrodes. REF 2059144-001 and 2059144-005. . Product Usage: Usage: Skintact Pediatric Multifunction Electrodes are for use on pediatric patients, less than 8 years of age, or weighing less than 25 kg…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0314-2015·2014-12-31
Chaotic Labz Recalls MAYHEM Capsules Containing Undeclared Prescription Drugs
Chaotic Labz is recalling MAYHEM capsules because FDA analysis found undeclared dexamethasone and cyproheptadine, making the product an unapproved drug.
Product
MAYHEM capsules, Proprietary Blend 525 mg, Dietary Supplement, 60-count bottles, Chaotic-Labz, UPC 6 28586 67805 7.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0859-2015·2014-12-31
Siemens ADVIA Centaur Laboratory Analyzer Recall for Tubing Crack Risk
Siemens is recalling ADVIA Centaur laboratory analyzers because a slight crack in the tubing at the reservoir connector may occur due to mechanical stress.
Product
ADVIA Centaur (including refurbished) Professional use in a laboratory for in vitro diagnostic tests.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0857-2015·2014-12-31
Iris Diagnostics Recalls RTH8 Rotor for StatSpin Express 4 Centrifuge
Iris Diagnostics is recalling RTH8 rotors for the StatSpin Express 4 Horizontal Centrifuge because the parts may develop cracks with use over time.
Product
RTH8 Rotor, P/N X01-005847-001. RTH8 used in the StatSpin Express 4 Horizontal Centrifuge, Model M510, Product No. SSH4. The RTH8 rotor is used with the Statspin Express 4 Horizontal Centrifuge. StatSpin Express 4 Centrifuge: For in vitro diagnostic use to produce the rapid…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0856-2015·2014-12-31
Horiba Lite DM Software Recall for Potential Data Mismatch
Horiba Instruments is recalling Lite DM software versions 2.0.0.19 and lower due to a bug that may apply test results to the wrong patient order.
Product
Lite DM (Lite Data Manager) Software Version(s): Versions 2.0.0.19 and lower Product Model #: D00A00224D The Lite DM (Lite Data Manager) is a software application developed by HORIBA Medical intended to receive, store, and manage Startup, Patient, and Quality Control (QC)…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0874-2015·2014-12-31
Ebi Solitaire-C Cervical Spacer Drill Sleeves Recalled for Design Deficiency
Ebi, LLC is recalling 193 units of Solitaire-C Cervical Spacer System drill sleeves because a design defect allows instruments to penetrate 1.0 mm beyond intended depths.
Product
Solitaire-C Cervical Spacer System a) 14-531593 Drill/Awl Sleeve b) 14-531594 Spring-Loaded Drill/Awl Sleeve Intended to stabilize cervical spinal segment to promote fusion in order to restrict motion and decrease pain using bone graft with or without supplemental…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0326-2015·2014-12-31
Neolpharma Recalls Subpotent Alprazolam Tablets Nationwide
Neolpharma, Inc. is voluntarily recalling 12,310 bottles of 0.25 mg alprazolam tablets nationwide because the medication was found to be subpotent.
Product
ALPRAZOLAM — ALPRAZOLAM (ALPRAZOLAM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0873-2015·2014-12-31
Radiometer HemoCue Glucose 201 Microcuvettes Recalled for Discoloration and Inaccurate Results
Radiometer America Inc. is recalling HemoCue Glucose 201 Microcuvettes because they show discoloration and provide results outside specification near the end of their shelf life.
Product
HemoCue¿ Glucose 201 Microcuvettes, The HemoCue Glucose 201 Microcuvettes are designed for use with the HemoCue Glucose 201Analyzer and the HemoCue Glucose 201 DM Analyzer (hereafter referred to as the HemoCue Glucose 201 Analyzer). HemoCue Glucose 201 Microcuvettes are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0832-2015·2014-12-31
Instrumentation Laboratory Recalls HemosIL PT-Fibrinogen HS PLUS Reagent
Instrumentation Laboratory is recalling HemosIL PT-Fibrinogen HS PLUS reagent kits because some vials exhibit discoloration that causes prolonged prothrombin clotting times.
Product
HemosIL PT-Fibrinogen HS PLUS, IVD --- Instrumentation Laboratory IL Company. A high sensitivity thromboplastin reagent based on recombinant human tissue factor (RTF) for the quantitative determination in human citrated plasma of Prothrombin Time (PT) and Fibrinogen on IL…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0319-2015·2014-12-31
Walgreens Aspirin Free Tension Headache Caplets Recalled for Undeclared Sucralose
LNK International recalled specific lots of Walgreens Aspirin Free Tension Headache Caplets because they contain sucralose, an ingredient not listed on the label.
Product
Walgreens ASPIRIN FREE TENSION HEADACHE, Pain Reliever/Pain Reliever Aid, Acetaminophen & Caffeine, 100 Coated Caplets, OTC --- Distributed by: Walgreen Co. 200 Wilmot Rd., Deerfield, IL 60015, Item # 427594, NDC 0363-0428-12, UPC Code 311917134925
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0839-2015·2014-12-31
Unapproved Dental Implants Recalled by Instradent USA
Instradent USA is recalling 13 units of Neodent Titamax WS Cortical Implants because the product is not approved for use in the US.
Product
Neodent Titamax WS Cortical Implant ¿4.0 x 5 mm (Endosseous dental implant) Article Number: 109.604 Dental implants are intended for surgical placement in maxillary and/or mandibular arches to provide support for prosthetic restorations in edentulous or partially edentulous…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0325-2015·2014-12-31
Zydus Recalls Benzonatate Capsules Due to Wet or Leaking Defects
Zydus Pharmaceuticals USA is recalling 19,536 units of Benzonatate capsules because some are wet or leaking. The recall is nationwide.
Product
BENZONATATE — BENZONATATE (BENZONATATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0320-2015·2014-12-31
Sunmark Eye Drops Recalled for Non-GMP API Storage
K C Pharmaceuticals is recalling Sunmark Eye Drops because the active ingredient was stored in a non-GMP compliant warehouse in Italy.
Product
SUNMARK EYE DROPS ORIGINAL FORMULA — SUNMARK EYE DROPS ORIGINAL FORMULA (TETRAHYDROZOLINE HCL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0875-2015·2014-12-31
Zimmer Recalls Trilogy Fiber Metal Acetabular Shell Due to Thread Defect
Zimmer Manufacturing B.V. is recalling 68 units of Trilogy Fiber Metal Acetabular Shells because the polar-hole threads were found to be undersized, preventing proper attachment to surgical instruments.
Product
Trilogy¿ Fiber Metal Acetabular Shell Size 54 mm OD The Trilogy Acetabular System is indicated for either cemented or uncemented use in skeletally mature individuals undergoing primary or revision surgery for rehabilitating hips damaged as a result of noninflammatory…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0852-2015·2014-12-31
Getinge 46-Series Medical Washer-Disinfector Recalled for Sediment Residuals
Getinge Disinfection AB is recalling 46-Series Medical Washer-Disinfector models 46-4 and 46-5 due to sediment residuals in the manifold caused by air pockets.
Product
GETINGE 46-SERIES Medical Washer-Disinfector, Models 46-4 and 46-5, with PACS 300/350 Control Series with dryer --- Class II, exempt from 510(k) requirements. For use in healthcare facilities and laboratories where reusable items such as instruments, utensils, anesthesia…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0834-2015·2014-12-31
Intuitive Surgical Recalls Fluorescence Imaging Procedure Kits for Missing Storage Info
Intuitive Surgical is recalling Fluorescence Imaging Procedure Kits because storage conditions for indocyanine green are missing from the packaging.
Product
Fluorescence Imaging Procedure Kit, designed for use with Firefly Fluorescence Imaging for the da Vinci Si 3000 Surgical Systems. The Intuitive Surgical Endoscopic Instrument Control System (Intuitive Surgical da Vinci Surgical System Model IS3000) is intended to assist in the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0835-2015·2014-12-31
Intuitive Surgical Recalls Fluorescence Imaging Procedure Kits for Missing Storage Info
Intuitive Surgical is recalling Fluorescence Imaging Procedure Kits because storage conditions for indocyanine green are missing from the packaging.
Product
Fluorescence Imaging Procedure Kit, designed for use with Firefly Fluorescence Imaging for the da Vinci Xi 4000 Surgical Systems. The Intuitive Surgical Endoscopic Instrument Control System (Intuitive Surgical da Vinci Surgical System Model IS3000) is intended to assist in the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0833-2015·2014-12-31
GE Healthcare Recalls Centricity Enterprise Archive Software Due to Data Loss Risk
GE Healthcare is recalling Centricity Enterprise Archive software versions 4.0.x due to a potential data loss issue associated with HL-7 updates.
Product
Centricity Enterprise Archive is a software product for receiving, archiving and sending of medical data. DICOM devices (e..g. modalities, workstations) Communicate with the archive using the DICOM protocol (published by ACR-NEMA). The clinical use is limited to the interaction…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0860-2015·2014-12-31
Siemens ADVIA Centaur XP Immunoassay System Recalled for Tubing Crack Risk
Siemens Healthcare Diagnostics is recalling 10,515 ADVIA Centaur XP Immunoassay Systems because a slight crack may occur in the tubing at the reservoir connector assembly due to mechanical stress.
Product
ADVIA Centaur XP Immunoassay System (including refurbished) Professional use in a laboratory for in vitro diagnostic tests.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0321-2015·2014-12-31
KC Pharmaceuticals Recalls Eye Drops Due to Non-GMP API Storage
KC Pharmaceuticals is recalling 302,976 bottles of Eye Drops A.C. because the active ingredient was stored in a non-GMP compliant warehouse in Italy.
Product
Eye Drops A.C. (Tetrahydrozoline HCl 0.05%, Zinc sulfate 0.25%), 0.5 FL OZ (15 mL) Bottles, Over the Counter. Labeled: a) Astringent Redness Reliever, Distributed by Safeway Inc., P.O. Box 99, Pleasanton, CA 94566-0009, UPC: 3 21130 70067 8; b) Best Choice, Distributed By: Valu…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0322-2015·2014-12-31
K C Pharmaceuticals Recalls Eye Drops Due to Warehouse Storage Issues
K C Pharmaceuticals is recalling specific lots of Eye Drops Industrial Strength because the active ingredient was stored in a non-GMP compliant warehouse in Italy.
Product
Eye Drops Industrial Strength (Polyethylene glycol 400 1%, Tetrahydrozoline HCl 0.05%), 0.5 FL OZ (15 mL) Bottles, Over the Counter. Labeled: a) Manufactured for: Petragon, Inc., Edwardsville, KS 66111; b) SWIFT, Distributed by Swift First Aid, Inc., Valencia, Calif. 91355…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0323-2015·2014-12-31
KC Pharmaceuticals Recalls Sunmark Eye Drops for CGMP Deviations
KC Pharmaceuticals is recalling Sunmark Eye Drops Advanced Moisturizer/Lubricant because the active ingredient was stored in a non-GMP compliant warehouse in Italy.
Product
SUNMARK EYE DROPS ADVANCED MOISTURIZER/LUBRICANT — SUNMARK EYE DROPS ADVANCED MOISTURIZER/LUBRICANT (DEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0318-2015·2014-12-31
Sulfur8 Medicated Anti-Dandruff Conditioner Recalled for pH Specification Failure
J. Strickland and Co is recalling Sulfur8 Medicated Anti-Dandruff Conditioner because the product pH failed to meet specifications.
Product
sulfur8(R) medicated anti-dandruff conditioner, dandruff treatment for Braids, spray, Active Ingredient: Salicylic Acid, 2%, 12 FL OZ (356ml) spray bottle, OTC, Made in the U.S.A. J. Strickland & Co., OLIVE BRANCH, MS 38654 UPC: 0 7561044510 7
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0313-2015·2014-12-31
Hospira Recalls Dacarbazine Injection Vials Due to Discoloration
Hospira Inc. is recalling 3,306 vials of Dacarbazine Injection, USP, 200mg, because the reconstituted solution may appear pink instead of the expected colorless to pale yellow.
Product
Dacarbazine, Injection, USP, 200mg, vials packaged in individual cartons, Rx only, Manufactured by Hospira Australia 1 Lexia Place, Mulgrave, Victoria Australia 3170. NDC 61703-327-22.
Category
Drug
Distribution
Distributed nationwide