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.

55251–55275 of 73850

CriticalFDA (Food)·F-1045-2015·2015-02-18
Full Tilt Salted Caramel Ice Cream Recalled for Listeria Risk
Full Tilt Ice Cream is recalling Salted Caramel ice cream due to potential Listeria monocytogenes contamination from a recalled ingredient.
Product
Salted Caramel ice cream, labeled in part, "***Full Tilt ice cream Salted Caramel***Ingredients: cream, milk, sugar, skim milk powder, vanilla, carob bean gum, guar gum, soy lecithin, carrageenan, salt***Seattle WA 98106 www.fulltilticecream.com***". Ice cream is packaged…
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1049-2015·2015-02-18
Full Tilt Bumberberry Ice Cream Recalled for Listeria Risk
Full Tilt Ice Cream is recalling Bumberberry ice cream due to potential Listeria monocytogenes contamination from a recalled ingredient.
Product
Bumberberry ice cream, labeled in part, "***Full Tilt ice cream BUMBERBERRY***Ingredients: Cream, milk, sugar, skim milk, Washington blackberries, Washington blueberries, Washington strawberries, Washington raspberries, guar gum, carob bean gum, soy lecithin…
Category
Food
Distribution
Distributed nationwide
CriticalFDA (Food)·F-1047-2015·2015-02-18
Full Tilt Mexican Chocolate Ice Cream Recalled for Listeria Risk
Full Tilt Ice Cream is recalling Mexican Chocolate ice cream due to potential Listeria monocytogenes contamination from a recalled ingredient.
Product
Mexican Chocolate ice cream, labeled in part, "***Full Tilt ice cream Mexican Chocolate***Ingredients: Cream, milk, skim milk powder, sugar, bittersweet chocolate, corn syrup solids, dutch processed cocoa, vanilla, chocolate liquor, cinnamon, carob bean gum, guar gum, soy…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1052-2015·2015-02-18
Full Tilt Huckleberry Chip Ice Cream Recalled for Listeria Risk
Full Tilt Ice Cream is recalling Huckleberry Chip ice cream due to potential Listeria monocytogenes contamination from a recalled ingredient.
Product
Huckleberry Chip ice cream, labeled in part, "***Full Tilt ice cream Huckleberry Chip***Ingredients: Cream, milk, sugar, skim milk powder, huckleberries, chocolate chips (unsweetened chocolate, sugar, cocoa fat, soy lecithin, vanilla), vanilla, carob bean gum, corn syrup solids…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1057-2015·2015-02-18
Full Tilt Thai Iced Tea Ice Cream Recalled for Listeria Risk
Full Tilt Ice Cream is recalling Thai Iced Tea ice cream due to potential Listeria monocytogenes contamination from a recalled ingredient.
Product
Thai Iced Tea ice cream, labeled in part, "***Full Tilt ice cream Thai Iced Tea ***Ingredients: Cream, milk, skim milk, sugar, ceylon tea, cardamom, star anise, vanilla, corn syrup solids, carob bean gum, guar gum, soy lecithin, carrageenan***Seattle WA 98106…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1090-2015·2015-02-18
Stryker Recalls MEDPOR Surgical Implants Due to Potential Intraoperative Damage
Stryker is recalling MEDPOR Surgical Implants because they may crack or break during surgery. The recall affects 1,051 units distributed worldwide.
Product
MEDPOR Surgical Implant Contoured Two Piece Chin 5 mm; Part Number 86001; Lot Numbers A1405048, A1404026 Product Usage: MEDPOR Implants in block, sheet and pre-formed shapes are intended for non-weight-bearing applications of craniofacial reconstruction/cosmetic surgery and…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1046-2015·2015-02-18
Full Tilt Ube Ice Cream Recalled for Listeria Contamination Risk
Full Tilt Ice Cream is recalling Ube ice cream due to potential Listeria monocytogenes contamination from a recalled ingredient.
Product
Ube ice cream, labeled in part, "***Full Tilt ice cream Ube***Ingredients: Cream, milk, sugar, skim milk powder, ube, corn syrup solids, carob bean gum, guar gum, soy lecithin, carrageenan, natural flavoring***Seattle WA 98106 www.fulltilticecream.com***". Ice cream is…
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·15V092000·2015-02-18
Land Rover Recalls 2015 Models for Cracking Wheel Lug Nuts
Jaguar Land Rover is recalling 2015 Range Rover, Range Rover Sport, and LR4 vehicles because wheel lug nuts may crack and detach, increasing crash risk.
Product
LAND ROVER — LAND ROVER RANGE ROVER SPORT, LR4, RANGE ROVER
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0385-2015·2015-02-18
Akorn Recalls Erythromycin Pledgets Due to Microbial Contamination
Akorn, Inc. is recalling Erythromycin Pledgets USP, 2%, 60-count jars because the active pharmaceutical ingredient failed USP microbial tests.
Product
Erythromycin Pledgets USP, 2%, 60-count jar,Rx only, Manufactured by Ei LLC, Kannapolis, NC 28083, Marketed by VersaPharm Incorporated, Marietta, GA 30062, NDC 61748-202-60 .
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-1059-2015·2015-02-18
Full Tilt Mudhoney Ice Cream Recalled for Listeria Risk
Full Tilt Ice Cream is recalling Mudhoney ice cream due to potential Listeria monocytogenes contamination from a recalled ingredient.
Product
Mudhoney ice cream, labeled in part, "***Full Tilt ice cream Mudhoney***Ingredients: Cream, milk, sugar, skim milk powder, chocolate chips (unsweetened chocolate, sugar, cocoa fat, soy lecithin, vanilla), honey, cinnamon, vanilla, carob bean gum, guar gum, soy lecithin…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1091-2015·2015-02-18
Stryker Recalls MEDPOR BARRIER Sheets for Potential Deformation and Cracking
Stryker is recalling MEDPOR BARRIER Sheets due to risks of deformation, cracking, and loss of adhesion during surgery.
Product
MEDPOR BARRIER Sheets Orbital Floor Implant Product Usage: MEDPOR Implants in block, sheet and pre-formed shapes are intended for non-weight-bearing applications of craniofacial reconstruction/cosmetic surgery and repair of craniofacial trauma. MEDPOR Surgical Implants and…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1196-2015·2015-02-18
Freeland Foods Recalls Organic Sunflower Seeds Due to Salmonella
Freeland Foods is recalling Go Raw 100% Organic Sunflower Seeds because CFIA detected Salmonella in the product.
Product
Go Raw 100% Organic Sunflower Seeds; Net Wt. 1 lb (454 g) USDA Organic UPC 8 59888 00009 7 Ingredients: Sprouted Organic Sunflower seeds, Celtic Sea Salt. All Handmade by Freeland Foods Mountain View, CA 94040
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-1056-2015·2015-02-18
Full Tilt Strawberry Basil Ice Cream Recalled for Listeria Risk
Full Tilt Ice Cream is recalling Strawberry Basil ice cream due to potential Listeria monocytogenes contamination from a recalled ingredient.
Product
Strawberry Basil ice cream, labeled in part, "***Full Tilt ice cream Strawberry Basil***Ingredients: Cream, milk, skim milk powder, sugar, Strawberries, basil, corn syrup solids, carob bean gum, guar gum, soy lecithin, carrageenan***Seattle WA 98106 www.fulltilticecream.com***".…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D0384-2015·2015-02-18
AnazaoHealth Recalls Compounded Plaquex Intravenous Injection Due to Unapproved Ingredient Source
AnazaoHealth Corporation is recalling 51 vials of Compounded Plaquex intravenous injection nationwide because the product contains an active pharmaceutical ingredient from an unapproved source.
Product
Compounded Plaquex, intravenous injection, 50 ML vial. Each ml contains: Phosphatidyl Choline 50 mg, Sodium Deoxycholate 25 mg, Benzyl Alcohol 0.9%, Ethanol (95%) 2.4 mg di Alpha Tocopheryl Acetate 0.2 mg in Sterile Water for injection.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1092-2015·2015-02-18
Stryker Recalls MEDPOR BARRIER Sheets Due to Deformation and Cracking Risks
Stryker is recalling MEDPOR BARRIER Sheets due to potential implant deformation, mechanical instability, and cracking during surgery.
Product
MEDPOR BARRIER Sheets Rectangle Product Usage: MEDPOR Implants in block, sheet and pre-formed shapes are intended for non-weight-bearing applications of craniofacial reconstruction/cosmetic surgery and repair of craniofacial trauma. MEDPOR Surgical Implants and MEDPOR…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·15V091000·2015-02-18
Jaguar Recalls 2013 XF Vehicles for Fuel Pump Shutdown Risk
Jaguar is recalling 2013 XF vehicles because the fuel pump may shut down, causing the vehicle to stall and lose power-assisted braking and steering.
Product
JAGUAR — JAGUAR XF
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1064-2015·2015-02-18
Virtual Imaging Recalls Digital Mobile X-ray Systems Due to Motion Defect
Virtual Imaging, Inc. is recalling 316 digital mobile X-ray systems in the US and 6 in Canada due to a potential for unintended and erratic motion.
Product
Digital Mobile X-ray Systems used to take diagnostic radiographic exposures or patients.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1100-2015·2015-02-18
Teleflex Medical Recalls Aquapak 340 SW Humidifier Adaptors for Foreign Material
Teleflex Medical is recalling Aquapak 340 SW humidifier adaptors because the packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
Product
AQUAPAK 340 SW, 340 ML W/040 ADAPTOR, FREN. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1087-2015·2015-02-18
Siemens Symbia T Series Medical Imaging Systems Recalled for Bearing Failure
Siemens Medical Solutions is recalling Symbia T series imaging systems because a linear bearing car may fail, allowing ball bearings to fall out.
Product
The Siemens Symbia T series is intended to aid in detecting, localizing, diagnosing, staging and restaging of lesions, tumors, disease and organ function for the evaluation of diseases and disorders. The images produced by the system can also be used by the physician to aid in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1101-2015·2015-02-18
Teleflex Medical Recalls Aquapak 340 Humidifier Adaptors Due to Foreign Material
Teleflex Medical is recalling Aquapak 340 Humidifier Adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
Product
AQUAPAK 340 SW, 340, ML W/040, ADAPTOR, JAPA. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1102-2015·2015-02-18
Teleflex Medical Recalls Aqua 540 Humidifier Adaptors Due to Foreign Material
Teleflex Medical is recalling Aqua 540 Humidifier Adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
Product
AQUA 540 SW, 540 W/040 ADAPTOR. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor packaged with…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1084-2015·2015-02-18
Integra Recalls Mayfield Ultra 360 Base Units Due to Locking Handle Failure
Integra LifeSciences is recalling 1,053 Mayfield Ultra 360 Base Units because the locking handle mechanism may fail during use, posing a risk to patients.
Product
The MAYFIELD¿ Ultra 360 Base Unit for head positioner, one unit per package. Product Usage: This product provides the ability to position and hold a patient head while the patient is in the prone, supine, lateral or park-bench and sitting positions. It is intended to be…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1086-2015·2015-02-18
Siemens Symbia S Series Medical Imaging Systems Recalled for Bearing Failure
Siemens Medical Solutions is recalling 719 Symbia S series systems because a linear bearing car may fail, allowing ball bearings to fall out.
Product
The Siemens Symbia S series is intended to aid in detecting, localizing, diagnosing, staging and restaging of lesions, tumors, disease and organ function for the evaluation of diseases and disorders. The images produced by the system can also be used by the physician to aid in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1107-2015·2015-02-18
Teleflex Medical Recalls 040 Humidifier Adaptors Due to Foreign Material
Teleflex Medical is recalling 040 Humidifier Adaptors because packages may contain black particles. The recall affects 15,779,607 units distributed worldwide.
Product
ADAPTOR, 040 HUM, INTL. Product Usage: The Humidifier Adaptor is an accessory which allows connection of sterile water or sterile saline to a humidifier circuit for the addition of water vapor to inhalation therapy gases. Only the 040 Humidifier adaptor packaged with the…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·15E009000·2015-02-18
Gillig Recalls S26 Eaton Hydraulic Pumps for Steering Effort Changes
Gillig LLC is recalling 177 S26 Eaton-brand hydraulic pumps sold between 2011 and 2014. The pumps may have manufacturing inconsistencies causing unexpected steering effort changes.
Product
STEERING:HYDRAULIC POWER ASSIST:PUMP recall
Category
Vehicle
Distribution
Distributed nationwide