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.

53451–53475 of 73847

HighFDA (Devices)·Z-1775-2015·2015-06-17
Philips Medical Systems Recalls AXIS UPS Accessory Devices for CT Systems
Philips Medical Systems is recalling AXIS Uninterruptible Power Supply (UPS) accessory devices used with CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.
Product
AXIS (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1777-2015·2015-06-17
Philips Medical Systems Recalls Forte-JetStream AZ UPS Accessory Devices
Philips Medical Systems is recalling 11 Forte-JetStream AZ UPS accessory devices used in CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fumes.
Product
Forte-JetStream AZ (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1790-2015·2015-06-17
Philips BrightView X UPS Accessory Devices Recalled for Battery Acid Leakage
Philips Medical Systems is recalling 108 BrightView X UPS accessory devices used with CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.
Product
BrightView X (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1771-2015·2015-06-17
Philips Medical Systems Recalls Ingenuity Core UPS Accessory Devices
Philips Medical Systems is recalling 215 Ingenuity Core UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.
Product
Ingenuity Core (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1714-2015·2015-06-17
ASP Recalls EVOTECH Endoscope Cleaner for Connection Detection Failure
Advanced Sterilization Products is recalling EVOTECH Endoscope Cleaner and Reprocessor units because they may fail to detect disconnected endoscopes, allowing the cleaning cycle to complete without proper processing.
Product
EVOTECH Endoscope Cleaner and Reprocessing System 208V, P/N 50004. The ASP EVOTECH ECR Endoscope Cleaner and Reprocessor is a washer/disinfector, which is indicated for use with high-level disinfectant CIDEX OPA Concentrate and an enzymatic detergent (CIDEZYME Gl) to achieve…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1763-2015·2015-06-17
Philips Brilliance CT 40 Uninterruptible Power Supply Recall
Philips is recalling Brilliance CT 40 Uninterruptible Power Supply accessories due to risks of battery acid leakage, overheating, and fume emission.
Product
Brilliance CT 40 - Slices(Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1788-2015·2015-06-17
Philips Recalls GEMINI TF Ready UPS Accessory Devices for CT Systems
Philips Medical Systems is recalling three GEMINI TF Ready UPS accessory devices used with CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fumes.
Product
GEMINI TF Ready (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1758-2015·2015-06-17
Edwards Lifesciences IntraClude Intra-Aortic Occlusion Device Recalled for Potential Damage
Edwards Lifesciences is recalling IntraClude Intra-Aortic Occlusion Devices due to potential damage near the hub that may cause blood leakage.
Product
Edwards Lifesciences IntraClude Intra-Aortic Occlusion Device, model number ICF100, 10.5 Fr (3.5 mm) x 39.4" (100 cm) ThruPort System. Packaged sterile and non-pyrogenic in a sealed, peel-type pouch For use in patients undergoing cardiopulmonary bypass.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1719-2015·2015-06-17
Elekta Recalls Leksell GammaPlan Software Due to Memory Corruption
Elekta is recalling 10 units of Leksell GammaPlan 10.2 software because memory can become corrupted when creating a fused study via drag and drop.
Product
Laksell GammaPlan, a computer based dose planning system specifically designed for use with Leksell Gamma Knife, radiation therapy treatment.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1768-2015·2015-06-17
Philips Brilliance iCT UPS Accessory Devices Recalled for Battery Acid Leakage
Philips Medical Systems is recalling Brilliance iCT UPS accessory devices due to risks of battery acid leakage, overheating, and fume emission.
Product
Brilliance iCT (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1774-2015·2015-06-17
Philips FORTE UPS Accessory Devices Recalled for Battery Acid Leakage Risk
Philips Medical Systems is recalling 10 FORTE Uninterruptible Power Supply (UPS) accessory devices used with CT and diagnostic imaging systems due to risks of battery acid leakage, overheating, and fume emission.
Product
FORTE (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1741-2015·2015-06-17
Biomet Recalls Unilateral External Fixation Ankle Clamps Due to Assembly Error
Biomet, Inc. is recalling 19 unilateral external fixation ankle clamps because they were assembled incorrectly. The defect may prevent full range of motion and cause the pin to loosen from the bone.
Product
Unilateral external fixation ankle clamp Product Usage: Unilateral external fixation for use treatment of bone conditions amenable to treatment by use of external fixation modality
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1725-2015·2015-06-17
Abbott Alkaline Wash Recall Due to Cap Leaking and Crystallization
Abbott Laboratories is recalling Alkaline Wash cleaning solution for Abbott Architect analyzers due to product leaking from the cap and crystallization around the cap.
Product
Alkaline Wash, List number 9D31-20, a cleaning solution used by the Abbott Architect analyzers. It is supplied in 500 mL bottles and contains NaOCl, NaOH, and KOH. It is shipped and stored at room temperature and is shipped ready to use.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1729-2015·2015-06-17
Ortho-Clinical Diagnostics Recalls VITROS Urine Assay Data Disks
Ortho-Clinical Diagnostics is recalling VITROS Urine Assay Data Disks because a software error may allow samples requiring acidified pretreatment to be metered from the same container as those requiring no pretreatment.
Product
Assay Data Disk (ADD), All DRV versions that support product within expiry dating 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…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1116-2015·2015-06-17
Valeant Recalls Nifedipine Extended-Release Tablets Due to Dissolution Failures
Valeant Pharmaceuticals is recalling Nifedipine Extended-Release Tablets, 90 mg, because some lots failed dissolution specifications.
Product
Nifedipine Extended-Release Tablets, USP, 90 mg, 100 Tablet Bottles, Rx Only. Manufactured for: Teva Pharmaceuticals USA Sailorsville, PA 13960. Manufactured in Canada By: Valeant Pharmaceuticals International, Inc. Steinbach, MB R5G 127 Canada. NDC: 0093-2059-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1129-2015·2015-06-17
Akorn Recalls Hydroxyzine Hydrochloride Oral Solution Due to Impurity Failures
Akorn, Inc. is recalling 424,174 bottles of Hydroxyzine Hydrochloride oral solution because the product failed impurities and degradation specifications.
Product
Hydroxyzine Hydrochloride, oral solution, 10 mg per 5 mL, 16 fl oz (473 ml) bottle, Rx only, Manufactured for KVK-Tech, Inc., Newtown, PA by Hi-Tech Pharmacal Co., Inc., Amityville, NY, NDC 10702-0052-16
Category
Drug
Distribution
Distributed nationwide
ModerateUSDA FSIS·093-2015·2015-06-17
Pinnacle Foods Recalls Swanson Turkey Dinners for Undeclared MSG
Pinnacle Foods is recalling approximately 668,316 pounds of Swanson Stuffing Baked Turkey dinners because the product contains monosodium glutamate (MSG) that is not declared on the label.
Product
Recall Notification Report 093-2015 (Poultry Products )
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1746-2015·2015-06-17
Becton Dickinson Recalls BBL Port A Cul Tubes Due to Oxidation
Becton Dickinson is recalling BBL Port A Cul tubes because excessive oxidation may affect the viability of anaerobic microorganisms.
Product
BBL Port A Cul tubes, catalog number 221606. Patient sample collection tubes. BBL Port A Cul tubes, jars and vials contain a reduced transport medium and are intended to maintain the viability of anaerobic, facultative and aerobic microorganisms during transport from the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1720-2015·2015-06-17
Roscoe Mini Neb Compressor User Manual Recall for Warning Updates
Compass Health Brands is recalling 219,353 Roscoe Mini Neb Compressor user manuals to add warnings about proper handling and storage to reduce power cord damage.
Product
Roscoe Mini Neb Compressor User Manual for the NEB-ROS Product Usage: Inhaler therapy that converts liquid medicine into a fine mist that is easily inhaled.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1754-2015·2015-06-17
Biomet Recalls Hip Components Due to Incorrect GTIN Labeling Codes
Biomet is recalling specific hip joint replacement components because the device labeling contains incorrect Global Trade Identification Number (GTIN) codes.
Product
Mallory/Head Primary Hip System; Size 11, 160 mm, Lateralized Femoral Stem; Ti-6Al-4V; Porous Plasma Uncemented, & Mallory/Head Total Hip System Size 12, 165 mm, Bi- Metric Femoral Components. Hip joint replacement components include: femoral stems, femoral heads, acetabular…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1755-2015·2015-06-17
Biomet Shoulder Joint Replacement Components Recalled for Incorrect GTIN Codes
Biomet, Inc. is recalling specific shoulder joint replacement components because the device labeling contains incorrect Global Trade Identification Number (GTIN) codes.
Product
Comprehensive Shoulder System, 4 mm, 122 mm long, Primary Shoulder Stem, Ti-6Al-4V, Standard Length Porous Plasma. Shoulder joint replacement components include humeral stems, humeral heads, and glenoid components.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1756-2015·2015-06-17
Biomet Knee Joint Replacement Components Recalled for Incorrect GTIN Codes
Biomet is recalling MCK Maximum Congruent Knee System components because the device labeling contains incorrect Global Trade Identification Number (GTIN) codes.
Product
MCK Maximum Congruent Knee System, BIOMET FINNED PRI STEM 40MM; 80 x 10MM; 80 x 12.5 MM; 80 x 15 MM Knee joint replacement prostheses components include femoral, tibial, and patellar components.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1757-2015·2015-06-17
Biomet Recalls Hip Joint Components Due to Incorrect GTIN Labeling
Biomet is recalling 1,315 hip joint replacement components because the device labeling contains incorrect Global Trade Identification Number (GTIN) codes.
Product
Biomet Cobalt-Chrome Femoral Components, 32MM MOD HEAD COCR -6MM NECK; 32MM MOD HEAD COCR -3 MM NECK; 32MM MOD HEAD COCR STD NECK ; 32MM MOD HEAD COCR +3MM NECK; 32MM COCR MOD HD +6MM NO SKIRT Hip joint replacement components include: femoral stems, femoral heads, acetabular…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·15V380000·2015-06-16
Elgin Megawind-MX Street Sweepers Recalled for Boom Mounting Pin Defect
Elgin is recalling 2009-2015 Megawind-MX street sweepers because boom mounting pins may lose retaining pins, allowing the boom to detach and increasing crash risk.
Product
ELGIN — ELGIN MEGAWIND-MX
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·15V376000·2015-06-16
EverGreen Recalls 2015 Travel Trailers Due to Wheel Stud Defect
EverGreen is recalling 2015 i-Go, Ever-Lite, Sun Valley, and Ascend travel trailers because wheel studs may break, potentially causing the wheel to detach.
Product
EVERGREEN — EVERGREEN SUN VALLEY, EVER-LITE, I-GO, ASCEND
Category
Vehicle
Distribution
Distributed nationwide