State

Northern Mariana Islands product recalls

72,971 recalls have nationwide distribution and so reach Northern Mariana Islands. 22 additional recalls listed Northern Mariana Islands specifically in their distribution scope.

What the numbers show

Total: 22
Critical: 0
Severe: 8
Most recent: 2025-02-05

Of the 22 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 8 (36%) are Severe.

Which agencies issued them

These figures cover only the 22 recalls whose distribution notice names Northern Mariana Islands specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6151–6175 of 72993

SevereFDA (Drugs)·D-0465-2025·2025-06-18
Dietary Supplement Electro Buzz Recalled for Undeclared Active Pharmaceutical Ingredients
SAINI TRADE INC is recalling ELECTRO BUZZ dietary supplement (lot KT-1ST-43-01-07/2024, expiring 10/15/2026) distributed nationwide. Laboratory testing found undeclared chloropretadalafil, propoxyphenylsildenafil, and sildenafil.
Product
ELECTRO BUZZ, Dietary Supplement, 10 capsules per box, Distributed By: Health Fixer, Tempe, AZ 85288, UPC B0DK68LF6J.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1936-2025·2025-06-18
Philips SmartPath to dStream 1.5T MRI Gradient Coil Fire Risk
Philips SmartPath to dStream for 1.5T MRI systems are recalled due to potential gradient coil component failure that may produce smoke and fire, posing risks of inhalation injury, burns, asphyxia, and death.
Product
SmartPath to dStream for 1.5T¿; Product Number: 782146;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0463-2025·2025-06-18
Dietary Supplement Male Ultra Recalled for Undeclared Drug Ingredients
Male Ultra dietary supplement, distributed nationwide in 3,000 boxes, has been recalled because laboratory testing found it contains undeclared pharmaceutical ingredients: propoxyphenylsildenafil and sildenafil. The product was marketed without FDA approval.
Product
Male Ultra, Unleash Your Force, Dietary Supplement,10 capsules per box, Distributed By; Health Fixer, Tempe, AZ 85288, UPC B0CMQ4FTHG.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0459-2025·2025-06-18
Celecoxib Capsules 200 mg recalled for foreign tablets inside bottles
Alembic Pharmaceuticals is recalling Celecoxib 200 mg capsules after a customer found a Tadalafil 5 mg tablet inside a sealed 500-count bottle. The contamination was discovered through a customer complaint.
Product
Celecoxib Capsules, 200 mg, 500-count bottle, Rx only, Manufactured by: Alembic Pharmaceuticals Limited (Formulation Division), Panelav 389350, Gujarat, India, Manufactured for: Alembic Pharmaceuticals, Inc., Bedminster, NJ 07921, USA, NDC 62332-142-71
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·25V413000·2025-06-18
Mazda CX-50 airbag module software may cause improper deployment
Mazda is recalling certain CX-50 Hybrid and CX-50 vehicles because incorrectly configured module software may cause the airbag to deploy improperly. All affected vehicles are under dealer control.
Product
MAZDA — MAZDA CX-50 HYBRID, CX-50
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1952-2025·2025-06-18
Tecfen Medical 2.8mm Slit Knife Angled Sterility Assurance Recall
Tecfen Medical is recalling 2.8mm Slit Knife, Angled (Model QKN2808) ophthalmic surgical instruments due to sterility assurance concerns. Affected units were distributed in the US and internationally.
Product
Brand Name: Tecfen Medical Product Name: 2.8mm Slit Knife, Angled Model/Catalog Number: QKN2808 Software Version: No software Product Description: This is an ophthalmic knife (manual) that is to be sterile (gamma radiation) and packaged individually in Tyvek 1059B. Slit knive
Category
Medical Device
Distribution
Distributed nationwide
SevereCPSC·25351·2025-06-18
MaxKare Electric Blankets Recalled for Burn and Fire Hazards
MaxKare electric blankets (model HB18A) sold on Walmart.com can overheat and catch fire, posing burn hazards. Yumo has received 34 reports of overheating, including 3 burn injuries and 2 fires.
Product
MaxKare Electric Blankets
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·25342·2025-06-18
AstroAI 4-Liter/6-Can Minifridges Recalled Due to Fire and Burn Hazards
AstroAI is recalling approximately 249,100 minifridges because the electrical switch can short circuit, causing fires and burn hazards. At least 70 incidents of smoking, burning, melting, or fire have been reported, including two fires that caused more than $360,000 in property damage.
Product
4 Liter/6 Can Minifridges
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1929-2025·2025-06-18
Philips Intera 1.5T Achieva IT Nova MRI System Gradient Coil Fire Risk
Philips is recalling one Intera 1.5T Achieva IT Nova MRI system due to a gradient coil component that may overheat and produce smoke or fire, posing risks of inhalation injury, burns, or death.
Product
Intera 1.5T Achieva IT Nova Product Number: 781175
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1868-2025·2025-06-18
Z-800WF Infusion System software verification defect recall
Zyno Medical LLC is recalling 613 units of the Z-800WF Infusion System because unreleased software versions were installed on distributed devices without verification or validation.
Product
Z-800WF Infusion System. Intended to provide intravenous infusion of parenteral fluids, blood, and blood products to a patient.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1865-2025·2025-06-18
Z-800 Infusion System recalled for unverified software installation
Zyno Medical LLC is recalling 613 units of the Z-800 Infusion System distributed nationwide because unreleased software versions were installed on the devices without verification or validation.
Product
Z-800 Infusion System. Intended to provide intravenous infusion of parenteral fluids, blood, and blood products to a patient.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0466-2025·2025-06-18
Dietary Supplement ULTRA ARMOR Recalled for Undeclared Drug Ingredients
ULTRA ARMOR dietary supplement, distributed by Health Fixer, is recalled nationwide because it contains undeclared pharmaceutical ingredients propoxyphenylsildenafil and sildenafil. The product was marketed without FDA approval.
Product
ULTRA ARMOR, My Armor My Power, Dietary Supplement, 10 capsules per box, Distributed by Health Fixer, Tempe, AZ 85288, UPC B0CYJ7Y5H9.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1932-2025·2025-06-18
Philips Intera 1.5T Explorer/Nova Dual MRI Gradient Coil Fire Risk
Philips is recalling one Intera 1.5T Explorer/Nova Dual MRI system due to a gradient coil component that may overheat, produce smoke, or ignite, risking patient and operator injury.
Product
Intera 1.5T Explorer/Nova Dual Product Number: 781108;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0467-2025·2025-06-18
Male Ultra Pro dietary supplement recalled for undeclared pharmaceutical ingredients
Male Ultra Pro capsules are being recalled because laboratory testing found undeclared propoxyphenylsildenafil and sildenafil. The product was marketed without an approved New Drug Application.
Product
Male Ultra Pro, Unleash Your Force 2, 10 capsules per box, Distributed by: Health Fixer Tempe AZ 85288, UPC B0CZN7C6YH.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1921-2025·2025-06-18
SOLTIVE Premium SuperPulsed Laser System surgical instrument thermal incident
Olympus is recalling the SOLTIVE Premium SuperPulsed Laser System due to risk of thermal incidents including smoke, sparks, burning, or flames during clinical use caused by fiber fracturing.
Product
Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Premium SuperPulsed Laser System Model/Catalog Number: TFL-PLS, TFL-PLS-JA (Japan only); Software Version: N/A Product Description: SOLTIVE Laser Systems use technology to increase procedural efficiency and f
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1956-2025·2025-06-18
Contact Lens Insertion Solution Recalled for Potential Sterility Defect
Contamac Nutrifill Physiologic formula contact lens insertion solution is being recalled because it may lack sterility. The affected product was distributed nationwide.
Product
Contamac, Nutrifill Physiologic formula, Contact Lens Insertion solution
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V410000·2025-06-18
2026 Tesla Model Y and Model 3 Vehicles Seat Fastener Recall
Tesla is recalling certain 2026 Model Y and Model 3 vehicles because seat back fasteners may have been improperly tightened, potentially affecting proper occupant restraint during a crash.
Product
TESLA — TESLA MODEL Y, MODEL 3
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V416000·2025-06-18
REV Recalls 2025-2026 Fleetwood and Holiday Rambler Motorhomes for Electrical Defect
REV is recalling 2025-2026 Fleetwood Altitude and Holiday Rambler Incline motorhomes because water intrusion may cause electrical components to fail, potentially disabling carbon monoxide or propane detectors.
Product
FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER ALTITUDE, INCLINE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V418000·2025-06-18
Mazda Recalls 2025 CX-50 Hybrid for Gear Shifter Safety Issue
Mazda is recalling 2025 CX-50 Hybrid vehicles because the gear shifter can move to Drive without pressing the brake pedal, increasing crash risk.
Product
MAZDA — MAZDA CX-50 HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1957-2025·2025-06-18
KWIK-STICK Quality Control Kit for Culture Media Swab Mix-Up
Microbiologics Inc is recalling KWIK-STICK quality control kits because products were packaged with incorrect microorganism swabs, which may lead to delayed diagnosis of patient samples in clinical laboratories.
Product
KWIK-STICK, Quality control kit for culture media, Catalog Numbers 01065K, Oligella urethralis derived from ATCC¿ 17960; 0621K, Staphylococcus aureus derived from NCTC 12493
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1966-2025·2025-06-18
Allon 2001 Medical Device Heating System Malfunction Risk
Belmont Instrument's Allon 2001 device may heat water above safe limits if sensor connections fail and temperature alarms are disabled. The patient wrap may exceed its set temperature without user notification.
Product
Allon 2001. Part Number: 200-00263
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1939-2025·2025-06-18
Femoral Nail T2 GTN Left and Right Versions Mislabeled
Stryker GmbH is recalling certain Femoral Nail T2 GTN devices because some labeled as left version contained right nails, and vice versa. This mislabeling could result in incorrect surgical implantation.
Product
Femoral Nail, LEFT T2 GTN 8x300 mm. Catalog Number: 1850-0830S.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1954-2025·2025-06-18
Tecfen Medical 2.0mm Crescent Knife Ophthalmic Device Recall
Tecfen Medical is recalling 2.0mm Crescent Knife ophthalmic surgical instruments (Model QKN1010, Lot ZGY24071501-03) due to sterility assurance concerns. The affected devices were distributed in the US and internationally.
Product
Brand Name: Tecfen Medical Product Name: 2.0mm Crescent Knife Angled Bevel Up Model/Catalog Number: QKN1010 Software Version: No software Product Description: This is an ophthalmic knife (manual) that is to be sterile and packaged individually in Tyhvek 1059B. The crescent kn
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1973-2025·2025-06-18
BD TEXIUM Closed Male Luer Drug Transfer Device Recall
BD TEXIUM Closed Male Luer devices may leak at the interface between the closed male luer component and needle-free connector. The leak could cause procedure delays, treatment interruptions, exposure to hazardous drugs, and underdosing of medication.
Product
BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP, REF: 10012241-0500
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1970-2025·2025-06-18
Alaris Pump Infusion Sets may leak at male luer connections
BD Switzerland is recalling multiple Alaris Pump Infusion Set models worldwide due to potential leaks at the connection between the closed male luer component and needle-free connector, which could delay procedures, interrupt treatment, expose patients to hazardous drugs, or result in underdosing.
Product
Alaris Pump Infusion Set: SmartSite Bag Access Non-Vented Bonded Texium With Priming Cap Back Check Valve 2 SmartSite Y-Sites, REF: 10013361T; SmartSite Bag Access Non-Vented Bonded Texium Closed Male Luer With Priming Cap, REF: 10321213T; SmartSite Bag Access Non-Vented Low
Category
Medical Device
Distribution
Distributed nationwide