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.

56176–56200 of 73850

SevereFDA (Food)·F-0477-2015·2014-11-19
Protein supplement recalled for undeclared milk and shellfish allergens
Maine Natural Health, Inc. is recalling Recovery Vanilla dietary supplements because the labels fail to declare milk and shellfish allergens.
Product
Recovery Vanilla (also labeled Post Workout), Dietary Supplement Packaged under the labels: Maine Natural Health and Stronger Faster Healthier Packaged in: 2 lb (32 oz), 10 oz. and 30 gram sizes
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0494-2015·2014-11-19
Rejuvenate Natural Dietary Supplement Recalled for Undeclared Milk Allergen
Maine Natural Health, Inc. is recalling Rejuvenate Natural Dietary Supplement because it fails to declare the allergen milk.
Product
Rejuvenate Natural Dietary Supplement Packaged under the labels Stronger Faster Healthier: 2 lb (32 oz), and 10 oz sizes
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0476-2015·2014-11-19
Maine Natural Health Recalls Pure Whey Protein Supplement for Undeclared Milk
Maine Natural Health, Inc. is recalling Pure Whey Natural Dietary Supplement because the product fails to declare the allergen milk on the label.
Product
Pure Whey Natural Dietary Supplement Packaged under the labels: Maine Natural Health and Stronger Faster Healthier Packaged in: 2 lb (32 oz), 10 oz
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0484-2015·2014-11-19
Maine Natural Health Recalls Coconut Supplement for Undeclared Milk
Maine Natural Health, Inc. is recalling Endurance In Race Coconut Dietary Supplement because it fails to declare the allergen milk.
Product
Endurance In Race Coconut Dietary Supplement Packaged under the label Stronger Faster Healthier Pack. Packaged in: 2 lb (32 oz), and 30 gram sizes
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0488-2015·2014-11-19
Protein Supplement Recalled for Undeclared Milk Allergen
Maine Natural Health, Inc. is recalling Daily Balance Natural Dietary Supplement because it fails to declare milk as an allergen.
Product
Daily Balance Natural Dietary Supplement Packaged under the labels Stronger Faster Healthier: 2 lb (32 oz), and 10 oz sizes
Category
Food
Distribution
Distributed nationwide
SevereCPSC·15030·2014-11-19
AP Specialties Recalls Two-Tone Power Bank Chargers Due to Fire Hazard
AP Specialties is recalling about 172,000 Two-Tone Power Bank Chargers because they can overheat and cause a fire. Consumers should stop using the units and contact the company for a replacement.
Product
Two-Tone Power Bank Charger
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0188-2015·2014-11-19
GE Optima NM/CT 640 Recalled for Loose Camera Fasteners
GE Healthcare is recalling 29 Optima NM/CT 640 systems because loose fasteners could cause the camera to fall onto a patient during a scan.
Product
Optima NM/CT 640, Models H3100YA, H3100YC. Product Usage: The GE Optima NM/CT 640 system is intended for General Nuclear Medicine imaging procedures for detection of radioisotope tracer uptake in the patient body. It includes a general purpose Nuclear Medicine (NM) system…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0490-2015·2014-11-19
Protein Supplement Recalled for Failing to Declare Milk Allergen
Maine Natural Health is recalling Hunger and Weight Chocolate Dietary Supplement because it fails to declare the milk allergen.
Product
Hunger and Weight Chocolate Dietary Supplement Packaged under the labels Stronger Faster Healthier: 2 lb (32 oz), and 10 oz sizes
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0474-2015·2014-11-19
Maine Natural Health Recalls Pure Whey Vanilla Protein Supplement for Undeclared Milk
Maine Natural Health, Inc. is recalling Pure Whey Vanilla dietary supplements because the packaging fails to declare the allergen milk.
Product
Pure Whey Vanilla , Dietary Supplement Packaged under the labels: Maine Natural Health and Stronger Faster Healthier Packaged in: 2 lb (32 oz), 10 oz. and 30 gram sizes
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0486-2015·2014-11-19
Maine Natural Health Recalls Daily Balance Vanilla Supplement for Undeclared Milk
Maine Natural Health, Inc. is recalling Daily Balance Vanilla dietary supplements because they fail to declare the allergen milk. The recall covers 2 lb and 10 oz sizes distributed nationwide.
Product
Daily Balance Vanilla Dietary Supplement Packaged under the labels Stronger Faster Healthier: 2 lb (32 oz), and 10 oz sizes
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0483-2015·2014-11-19
Protein Supplement Recalled for Failing to Declare Milk Allergen
Maine Natural Health, Inc. is recalling Endurance Pre Race Pina Colada dietary supplements because they fail to declare the milk allergen.
Product
Endurance Pre Race Pina Colada, Dietary Supplement Packaged under the label Stronger Faster Healthier Pack. Packaged in: 2 lb (32 oz), and 30 gram sizes
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0186-2015·2014-11-19
GE Discovery NM/CT 670 Imaging System Recalled for Loose Fasteners
GE Healthcare is recalling 255 Discovery NM/CT 670 systems because loose fasteners may cause a portion of the system to fall onto patients during scans.
Product
Discovery NM/CT 670 dual detector free-geometry integrated nuclear imaging system. Models H3100NA, H3100PP, H3100RA, H2401LS, H2401LZ, H2402LS. Product Usage: The GE Discovery NM/CT 670 system is a medical tool intended for use by appropriately trained healthcare…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·14V741000·2014-11-19
Jaguar Recalls 2014-2015 XJ Models for Brake Line Leak Risk
Jaguar is recalling 2014-2015 XJ vehicles because brake line junctions may leak fluid, potentially reducing braking ability and increasing crash risk.
Product
JAGUAR — JAGUAR XJ
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·F-0501-2015·2014-11-19
Mondelez Recalls Chiclets Fruit Gum for Undeclared Soy Lecithin
Mondelez Global LLC is voluntarily recalling specific packages of Chiclets Fruit Flavor Gum because the label fails to declare soy lecithin.
Product
1) Chiclets Fruit Flavor Gum, 12 piece, Retail UPC 0 12546 10628 3; 2) Chiclets Fruit Flavor Gum, 20 - 12 piece packages (240 pieces), Retail UPC 0 12546 02503 4, Case UPC 10012
Category
Food
Distribution
Distributed nationwide
HighNHTSA·14V742000·2014-11-19
Champion Transit Buses Recalled for Wheelchair Lift Platform Cracking Risk
Champion Bus is recalling 2006-2014 transit buses equipped with certain Ricon wheelchair lifts because the platform side plate may crack, posing an injury risk.
Product
CHAMPION — CHAMPION AMERICAN COACH, HCAC, STACKED RAIL, PLATINUM SHUTTLE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·15031·2014-11-19
Mohawk Recalls Altitude Gold Shag Rugs Due to Fire Hazard
Mohawk Industries is recalling Altitude Gold shag rugs sold at The Home Depot because large sizes fail federal flammability standards, posing fire and burn risks.
Product
Altitude Gold shag rugs
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0209-2015·2014-11-19
American Medical Systems Recalls AMS 700 Series Inflatable Penile Prosthesis Accessory Kits
American Medical Systems is recalling AMS 700 Series Accessory Kits because supplier-supplied Keith needles may bend or break when used with the Furlow tool.
Product
AMS 700 Series Inflatable Penile Prosthesis Accessory Kit (AMS 700 Line Accessory Kit), 72401850. Keith Needles are part of the AMS 700 Accessory Kit. In conjunction with the Furlow Insertion Tool (Furlow), the Keith Needles facilitate the passing of the pulling sutures…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·15029·2014-11-19
Olympus Recalls Digital Audio Recovers Due to Overheating Burn Hazard
Olympus is recalling DS-5500 digital audio recorders because they can overheat while charging, posing a burn hazard to consumers and property.
Product
Olympus DS-5500 digital audio recorders
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-0503-2015·2014-11-19
Chiclets Gum Recalled for Undeclared Soy Lecithin
Mondelez Global LLC is voluntarily recalling Chiclets Gum because the label fails to declare soy lecithin, a common allergen.
Product
Chiclets Gum, 200 - 2 piece packs (400 pieces), Retail UPC 0 12546 02509 6, Case UPC 10012546108499
Category
Food
Distribution
Distributed nationwide
HighNHTSA·14V743000·2014-11-19
Toyota Recalls Vehicles Due to Seat Heater Wiring Fire Risk
Toyota is recalling specific models because seat cushion compression may damage heater wiring, creating a fire and injury risk.
Product
TOYOTA — TOYOTA HIGHLANDER, CAMRY, PRIUS, SEQUOIA
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·15034·2014-11-19
Hoppe's Recalls Semi-Auto Gun Bore Cleaner Due to Loose Cap
Hoppe's is recalling Semi-Auto Gun Bore Cleaner bottles because the child-resistant caps can become loose, posing a risk of chemical ingestion.
Product
Hoppe's Semi-Auto Gun Bore Cleaner
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0199-2015·2014-11-19
DePuy ATTUNE Intuition Distal Femoral Jig Recall for Bushing Defect
DePuy Orthopaedics is recalling ATTUNE Intuition Distal Femoral Jigs because a pin bushing defect could cause the plastic to fracture or displace during use.
Product
ATTUNE Intuition Distal Femoral Jig; sold non-sterile; product is wrapped in bubble wrap and then sealed inside a polyethylene bag
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·14E079000·2014-11-19
AFX Recalls FX-76 Motorcycle Helmets for Impact Test Failure
AFX North America is recalling specific FX-76 motorcycle helmets that failed federal impact tests. Riders may face serious injury in a crash.
Product
EQUIPMENT:MOTORCYCLE:HELMETS recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0183-2015·2014-11-19
Siemens Artis zeego C-arm systems recalled for cable routing defect
Siemens is recalling 164 Artis zeego systems because a cable may be routed incorrectly, potentially causing system failure during procedures.
Product
Artis zeego systems, model number 10280959, with serial numbers 1000-1599 : Artis zeego is a dedicated angiography system developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0213-2015·2014-11-19
Masimo SET uSpO2 Pulse Oximetry Cables Recalled for Crossed Wires
Masimo Corporation is recalling specific SET uSpO2 Pulse Oximetry Cables due to crossed internal wires that may cause the monitoring device to display inverted SpO2 values.
Product
Masimo SET uSpO2 Cable The Masimo SET uSpO2 Pulse Oximetry Cable is an in-line cable that provides continuous noninvasive monitoring of functional oxygen saturation of arterial hemoglobin (Sp02) and pulse rate when installed in a compatible OEM host system. Shipping/Package…
Category
Medical Device
Distribution
Distributed nationwide