State

Northern Mariana Islands product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49001–49025 of 73840

HighFDA (Devices)·Z-1377-2016·2016-04-20
Intuitive Surgical Recalls da Vinci S Surgical System User Manuals
Intuitive Surgical is recalling da Vinci S Surgical System user manuals because using non-approved instruments with ablation probes may increase microscopic metallic particulates.
Product
da Vinci S Surgical System (IS4000) user manual English and OUS. Product Usage: The Intuitive Surgical Endoscope Instrument Control System (da Vinci Surgical System, Model IS4000) is intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1386-2016·2016-04-20
Synthes Recalls SYNTHECEL Dura Repair Due to Adhesion Risks During Removal
Synthes (USA) Products LLC is recalling 378 units of SYNTHECEL Dura Repair because the device may adhere to anatomical structures if a surgeon attempts to remove it.
Product
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Device listing number: D140596, D211012 SYNTHECEL Dura Repair is intended for use as a dura replacement for the repair of dura mater in adults.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1363-2016·2016-04-20
Natus Medical Recalls Medix NatalCare ST-LX Neonatal Incubators
Natus Medical is recalling Medix NatalCare ST-LX neonatal incubators because defective hinge assemblies may cause ports to detach.
Product
Medix NatalCare ST-LX Intensive Care Incubator. Neonatal incubator.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1384-2016·2016-04-20
Synthes Recalls SYNTHECEL Dura Repair Due to Adhesion Risks
Synthes (USA) Products LLC is recalling 200 units of SYNTHECEL Dura Repair because the device may adhere to anatomical structures, posing risks if removal is attempted.
Product
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Device listing number: D140596, D211012 SYNTHECEL Dura Repair is intended for use as a dura replacement for the repair of dura mater in adults.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V229000·2016-04-20
Jaguar Recalls XF Vehicles Due to Driver Air Bag Defect
Jaguar is recalling certain 2009, 2011, 2012, and 2015 XF vehicles because the driver frontal air bag may deploy improperly, increasing injury risk.
Product
JAGUAR — JAGUAR XF
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1367-2016·2016-04-20
ICU Medical Recalls Diana Automated Compounding System Due to Accuracy Issues
ICU Medical is recalling 4 units of the Diana Automated Compounding System because compounded volumes under 5ml may not meet accuracy specifications.
Product
Diana Automated Compounding System, Diana Onco 3xx, Item No. ASN303 The Diana is an automated compounding device for the accurate, safe and efficient preparation of solutions by a pharmacist prior to delivery for infusion into patient.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1366-2016·2016-04-20
ICU Medical Recalls Diana Automated Compounding System Due to Accuracy Issues
ICU Medical is recalling 3 units of the Diana Automated Compounding System because compounded volumes under 5ml may not meet accuracy specifications.
Product
Diana Automated Compounding System, Diana Onco Plus 1.3, Item No. ASN223 The Diana is an automated compounding device for the accurate, safe and efficient preparation of solutions by a pharmacist prior to delivery for infusion into patient.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1371-2016·2016-04-20
Maquet QUADROX-i oxygenators recalled for potential endotoxin exposure
Maquet Cardiovascular is voluntarily recalling QUADROX-i oxygenators and tubing packs due to a potential risk of endotoxin exposure.
Product
QUADROX-i oxygenators Custom tubing packs for the oxygenator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1374-2016·2016-04-20
Maquet Custom Tubing Packs Recalled for Potential Endotoxin Exposure
Maquet Cardiovascular is voluntarily recalling 72,000 custom tubing packs for oxygenators due to a potential risk of endotoxin exposure.
Product
Custom Tubing Packs Custom tubing pack for oxygenators
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1395-2016·2016-04-20
C.R. Bard Recalls ArcticGel Pads Due to Flow Rate Issues
C.R. Bard is recalling 21,412 ArcticGel Pads used with the Arctic Sun Temperature Management System because of complaints regarding restricted or inaccurate flow rates.
Product
BARD ArcticGel Pads Product Usage: The Arctic Sun Temperature Management System is intended for monitoring and controlling patient temperature. ArcticGel Pads are only for use with an Arctic Sun Temperature Management System Control Module.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1369-2016·2016-04-20
ICU Medical Recalls Diana Automated Compounding System Due to Accuracy Issues
ICU Medical is recalling 49 units of the Diana Automated Compounding System because it may not meet accuracy specifications when mixing volumes under 5ml.
Product
Diana Automated Compounding System, Diana V1.3, Item No. CH5300, CH5300R The Diana is an automated compounding device for the accurate, safe and efficient preparation of solutions by a pharmacist prior to delivery for infusion into patient.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0824-2016·2016-04-20
Morrison Milling Recalls HEB Fish Fry Mix Due to Metal Fragments
Morrison Milling is recalling HEB Original Seasonal Fish Fry Mix because it may contain small metal fragments from a wire mesh sifter.
Product
HEB Original Seasonal Fish Fry Mix NET WT. 16 OZ (1 LB) CONT. NET 454g and HEB Original Seasonal Fish Fry Mix NET WT. 10 OZ CONT. NET 284g packed in paper box
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1387-2016·2016-04-20
Synthes Recalls SYNTHECEL Dura Repair Due to Adhesion Risks
Synthes (USA) Products LLC is recalling 317 units of SYNTHECEL Dura Repair because the device may adhere to anatomical structures, posing risks if removal is attempted.
Product
SYNTHECEL Dura Repair, 510K # K131792, K113071, Class II, Classification name: Dura Substitute Device listing number: D140596, D211012 SYNTHECEL Dura Repair is intended for use as a dura replacement for the repair of dura mater in adults.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·16149·2016-04-20
YTL International Recalls Drywall Lifts Due to Injury Hazard
YTL International is recalling about 17,000 drywall lifts because they can fail and drop loads, posing an injury risk. No injuries have been reported.
Product
Drywall lifts
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-1074-2016·2016-04-20
Hidden Valley Original Ranch Dressing Recalled for Missing Soy Label
The Clorox Company is recalling Hidden Valley Original Ranch dressing because some bottles are missing the soy lecithin ingredient declaration.
Product
Hidden Valley Original Ranch dressing, 16 fl oz. ( 473 ml). plastic bottles; Ingredients: Vegetable oil (soybean and/or Canola oil) water, egg yolk, sugar, Salt, Cultured non fat buttermilk, natural flavors (milk, soy), less than 1% spiced, dried garlic, dried onion, vinegar…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1380-2016·2016-04-20
Philips EPIQ Ultrasound Systems Recalled for Control Panel Fastener Loosening
Philips is recalling EPIQ diagnostic ultrasound systems because fasteners securing the control panel may loosen, potentially causing the assembly to detach.
Product
EPIQ DIAGNOSTIC ULTRASOUND SYSTEM, Model EPIQ 5C, EPIC 5G, EPIQ 5W, EPIQ 7C, EPIC 7GC, and EPIQ 7W. Diagnostic Ultrasound System for ultrasound imaging in abdominal, cardiac adult, cardiac other (fetal), cardiac pediatric, cerebral vascular, cephalic (adult), cephalic…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1373-2016·2016-04-20
Maquet Rotaflow Centrifugal Pump Tubing Recalled for Endotoxin Risk
Maquet Cardiovascular is voluntarily recalling Rotaflow Centrifugal Pump custom tubing packs due to a potential risk of endotoxin exposure.
Product
Rotaflow Centrifugal Pump Custom tubing packs for the oxygenator
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1376-2016·2016-04-20
Intuitive Surgical Recalls da Vinci S Surgical System User Manuals
Intuitive Surgical is recalling da Vinci S Surgical System user manuals because using certain instruments with ablation probes can increase microscopic metallic particulates.
Product
da Vinci S Surgical System (IS1200/IS2000/IS3000) user manual, instrument & accessory. Product Usage: The Intuitive Surgical Endoscopic Instrument Control System is intended to assist in the accurate control of Intuitive Surgical Endoscopic Instruments including rigid…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0864-2016·2016-04-20
Marie Callender's Corn Bread Mix Recalled for Metal Fragments
Morrison Milling is recalling Marie Callender's Low Fat Southwestern Corn Bread Mix because it may contain small metal fragments from a wire mesh sifter.
Product
Marie Callender's Low Fat Southwestern Corn Bread Mix NET WT 1 lb (16 oz. ) 454 grams
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1365-2016·2016-04-20
ICU Medical Recalls Diana Automated Compounding Systems for Accuracy Issues
ICU Medical is recalling 57 Diana Automated Compounding Systems because they may not accurately mix volumes under 5ml.
Product
Diana Automated Compounding System, Diana Onco Plus 1.2, Item No. ASN222, ASN222-GST, ASN222-R The Diana is an automated compounding device for the accurate, safe and efficient preparation of solutions by a pharmacist prior to delivery for infusion into patient.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0880-2016·2016-04-20
Pioneer Buttermilk Pancake Mix Recalled for Potential Metal Fragments
Morrison Milling is recalling Pioneer Original Buttermilk Pancake & Waffle Mix because it may contain small metal fragments from a wire mesh sifter.
Product
Pioneer Original Buttermilk Pancake & Waffle Mix NET WT 5 LBS 2.27 kg and Pioneer Original Buttermilk Pancake & Waffle Mix NET WT 25 LBS 11.34 kg
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1045-2016·2016-04-20
L'Bri Aloe Health Juice Drink Recalled for Unlabeled Sodium Metabisulfite
Cosmetic Labs LP is recalling L'Bri Pure N' Natural Nutri Aloe Health Juice Drink because it contains sodium metabisulfite, an ingredient not listed on the label.
Product
L'Bri Pure N' Natural Nutri Aloe Health Juice Drink 960 mL 32 FL. OZ. and L'Bri Pure N' Natural Nutri Aloe Health Juice Drink 1 FL OZ./29 mL
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0877-2016·2016-04-20
Conestoga Buttermilk Pancake Mix Recalled for Metal Fragment Risk
Morrison Milling is recalling Conestoga Buttermilk Pancake Mix because it may contain small metal fragments from a wire mesh sifter.
Product
Conestoga Buttermilk Pancake Mix NET WT. 5 LB. (2.27 kg)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0891-2016·2016-04-20
Morrison Milling Recalls Multigrain Pancake Mix Due to Metal Fragments
Morrison Milling is recalling American Blue Ribbon Multigrain Pancake Mix because it may contain small metal fragments from a wire mesh sifter.
Product
American Blue Ribbon Holdings. LLC Multigrain Pancake Mix NET WT 37.5 LBS (17.01 kg)
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1379-2016·2016-04-20
Stryker SurgiCounter Scanner Recalled for Software Interaction Errors
Stryker is recalling 286 SurgiCounter scanners because they may display error messages and fail to display software version numbers correctly in the SC360 application.
Product
SurgiCounter scanner, part of the SurgiCount Safety-Sponge System. Model numbers 0694-097-000 and 0694-097-001. Product Usage: The SurgiCount Safety Sponge System is indicated for use in counting and recording the number of thermally labeled surgical sponges, laparotomy…
Category
Medical Device
Distribution
Distributed nationwide