State

Northern Mariana Islands product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35726–35750 of 73760

HighFDA (Devices)·Z-0527-2019·2018-12-12
Barco Front Cover Attachment Kit Recalled for Potential Falling Hazard
Barco N.V. is recalling 2,087 MDRC-1119 Front Cover Attachment Kits because metal strips may deform, causing the protective cover to fall.
Product
Optional MDRC-1119 Front Cover Attachment Kit for review display monitors. Product Usage: The product is an optional kit, intended to be attached in front of the LCD panel of a review display (MDRC-1119).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0525-2019·2018-12-12
ASO Recalls Family Wellness Sterile Gauze Pads Due to Sterilization Concerns
ASO, LLC is recalling Family Wellness First Aid Sterile Gauze Pads because they may not be fully sterilized. The affected units were distributed nationwide to ten states.
Product
Family Wellness First Aid Sterile Gauze Pad 3 in x 3 in, 10 CT. White, bleached, non-woven, rayon/polyester sterile Gauze Pad 3 inch x 3 inch, 12-ply 10 count cardboard box
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0550-2019·2018-12-12
Capintec Recalls Captus 3000 Thyroid Uptake Systems Due to Spring Arm Failure
Capintec Inc is recalling 385 Captus 3000 Thyroid Uptake Systems because a broken tension rod can cause the spring arm to fail and the collimator to fall.
Product
Captus 3000 Thyroid Uptake System, Model # 5430-0076 and 5430-0077
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0531-2019·2018-12-12
Zimmer Biomet Recalls Humeral Guide Wires Due to Sterility Compromise
Zimmer Biomet is recalling specific lots of M/DN Intramedullary Fixation Humeral Guide Wires because creases in the packaging may compromise sterility.
Product
Zimmer M/DN¿ Intramedullary Fixation Humeral Guide Wire - Smooth, 2.4 mm Diameter, 70 cm Length Item Number: 00-2255-025-00 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·19046·2018-12-12
Stanley Commercial Hardware Locksets Recalled Due to Entrapment Risk
dormakaba USA is recalling Stanley Commercial Hardware locksets because they may fail to open, posing an entrapment hazard in emergencies. No injuries have been reported.
Product
Door locksets
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0535-2019·2018-12-12
Zimmer Biomet Recalls Guide Wires Due to Sterility Compromise
Zimmer Biomet is recalling ZMS Intramedullary Fixation Smooth Guide Wires because creases in the sealing area may compromise product sterility.
Product
Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire - Bullet Tip, 3.0 mm Diameter, 100 cm Length Item Number: 47-2237-038-00 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0530-2019·2018-12-12
Zimmer Biomet Recalls Pressure Sentinel Guide Wires Due to Sterility Compromise
Zimmer Biomet is recalling Pressure Sentinel Guide Wires because creases in the sealing area compromise product sterility. The recall affects 48,320 units distributed worldwide.
Product
Zimmer Pressure Sentinel¿ Intramedullary Reaming System, Guide Wire, Bullet Tip, 2.4 mm Diameter Item Number: 00-2228-024-00 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V886000·2018-12-12
Gillig Recalls 2016-2017 Low Floor Buses Due to Emergency Exit Defect
Gillig is recalling 2016-2017 Low Floor transit buses because an emergency exit window may be obstructed, hindering evacuation.
Product
GILLIG — GILLIG LOW FLOOR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0537-2019·2018-12-12
Zimmer Biomet Recalls Smooth Guide Wires Due to Sterility Compromise
Zimmer Biomet is recalling Smooth Guide Wires because creases in the sealing area may compromise product sterility. The recall affects 48,320 units distributed worldwide.
Product
Zimmer Smooth Guide Wire - Bullet Tip, 3.0 mm Diameter, 100 cm Length Item Number: 47-2255-008-01 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0547-2019·2018-12-12
Philips Brilliance 10 Slice CT Scanner Recalled for Gantry Cover Failure Risk
Philips is recalling Brilliance 10 Slice CT scanners because fiberglass resin may separate, causing the gantry front cover and metal support to fail or fall.
Product
Brilliance 10 Slice (Air), Model 728251 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·19047·2018-12-12
White-Rodgers Recalls Emerson Sensi WiFi Thermostats Due to Fire Hazard
White-Rodgers is recalling Emerson branded Sensi WiFi thermostats because contact between wires and household voltage can cause fire. No injuries have been reported.
Product
Emerson Branded Sensi WiFi thermostats
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0540-2019·2018-12-12
Zimmer Biomet Recalls Natural Nail System Guide Wires Due to Sterility Concerns
Zimmer Biomet is recalling 12,724 units of Natural Nail System Tear Drop Guide Wires because creases in the packaging may compromise sterility.
Product
Zimmer Natural Nail¿ System - Tear Drop Guide Wire, 3.0 mm Diameter, 70 cm Length Item Number: 47-2490-098-00 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0548-2019·2018-12-12
Philips Brilliance 6 Slice CT Scanner Recalled for Gantry Cover Separation Risk
Philips Medical Systems is recalling Brilliance 6 Slice CT scanners because fiberglass resin may separate, causing the gantry front cover to fail or fall.
Product
Brilliance 6 Slice (Air), Model 728256 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V882000·2018-12-12
Van Hool Recalls 2015-2018 Buses Due to Fire Extinguisher Defect
Van Hool is recalling 2015-2018 TD925 and TDX25 buses because the fire suppression system actuator may fail to discharge during a fire.
Product
VAN HOOL — VAN HOOL TD925, TDX25
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0557-2019·2018-12-12
Stephanix D2RS Digital Dynamic Remote System Recalled for Table Movement Risk
Stephanix is recalling 17 D2RS Digital Dynamic Remote Systems because the table may continue moving after a command is released.
Product
STEPHANIX D2RS Digital Dynamic Remote Systemhttp://cts.fda.gov/division-tracking/images/trash.png Product The D2RS Digital Dynamic Remote System is indicated for use in generating fluoroscopic images of human anatomy for vascular angiography, diagnostic and interventional…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0541-2019·2018-12-12
Zimmer Biomet Recalls Natural Nail System Tear Drop Guide Wires
Zimmer Biomet is recalling Natural Nail System Tear Drop Guide Wires due to creases in the sealing area that compromise sterility.
Product
Zimmer Natural Nail¿ System - Tear Drop Guide Wire, 2.4 mm Diameter, 70 cm Length Item Number: 47-2490-098-01 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0546-2019·2018-12-12
Philips Brilliance 16 Slice CT Scanner Recall for Cover Separation
Philips is recalling Brilliance 16 Slice CT scanners because fiberglass resin may separate, causing the gantry front cover to fail or fall.
Product
Brilliance 16 Slice (Air), Model 728246 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0543-2019·2018-12-12
Philips Brilliance 64 CT Scanner Recall for Gantry Cover Separation Risk
Philips Medical Systems is recalling Brilliance 64 CT scanners due to a potential fiberglass resin separation that could cause the gantry front cover to fail and fall.
Product
Brilliance 64, Model 728231 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0553-2019·2018-12-12
Zimmer Biomet Recalls 20mm Compress Device Short Anchor Plug
Zimmer Biomet is recalling 6 units of the 20mm Compress Device Short Anchor Plug due to potential metal burrs that may prevent proper insertion of drill and transverse pins.
Product
Biomet 20mm Compress Device Short Anchor Plug With Drill Set / With Pin Inserter Ion Implant Item number: 178562 Product Usage: 1. Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. 2. Tumor resections. 3. Revision of previously…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0556-2019·2018-12-12
Pfizer Recalls Thermacare Heatwraps Due to Material Leakage
Pfizer is recalling specific lots of Thermacare Heatwraps because the wraps may come apart and leak granular material.
Product
Thermacare HEATWRAPS JOINT PAIN THERAPY, 8 HEATWRAPS; MUSCLE PAIN THERAPY, 3 HEATWRAPS a) UPC 0573301311 b) UPC 0573301311 Product Usage: Provides heat therapy for temporary relief of minor muscular and joint aches and pains associated with overexertion, sprains, and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0555-2019·2018-12-12
Pfizer Recalls Thermacare HeatWraps Menstrual Due to Material Leakage
Pfizer is recalling Thermacare HeatWraps Menstrual because the wraps may come apart and leak granular material.
Product
Thermacare HeatWraps Menstrual a) UPC 0573302002 b) UPC 0573302044 Product Usage: Provides heat therapy for temporary relief of minor menstrual cramp pain and associated back aches.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0559-2019·2018-12-12
Tosoh AIA-360 Analyzer Recalled for Labeling Clarifications on Maintenance Requirements
Tosoh Bioscience is recalling 1,228 AIA-360 Analyzers to update labeling and training materials regarding maintenance and reagent requirements.
Product
AIA-360 Analyzer, product code 019945/019945R The Tosoh AIA-360 Automated Immunoassay Analyzer is for use in vitro diagnostic to provide testing for a broad menu of assays in a unique patented dry reagent format.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0528-2019·2018-12-12
Becton Dickinson Recalls Trypticase Soy Agar Plates Due to Growth Inhibition
Becton Dickinson is recalling 54,300 plates of Trypticase Soy Agar with 5% Sheep Blood because a manufacturing error inhibited the growth of Gram-negative organisms.
Product
BD BBL Trypticase Soy Agar with 5% Sheep Blood, Catalog No. 221261, (non-selective, non-differential)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0554-2019·2018-12-12
Pfizer Recalls Thermacare HeatWraps Due to Leaking Granular Material
Pfizer is recalling Thermacare Muscle Pain Therapy HeatWraps because the wraps may come apart and leak granular material.
Product
Thermacare Muscle Pain Therapy HeatWraps: a) UPC 0573301314 b) UPC 0573301303 Product Usage: Provides heat therapy for temporary relief of minor muscular and joint aches and pains associated with overexertion, sprains, and arthritis.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0529-2019·2018-12-12
Helena Laboratories Recalls Gel Alkaline Phosphatase Isoenzyme Control Kits
Helena Laboratories is recalling 43 Gel Alkaline Phosphatase Isoenzyme Control Kits due to customer complaints of lower enzyme activity.
Product
Gel Alkaline Phosphatase Isoenzyme Control Kit: Gel Alkaline Phosphatase Isoenzyme Control Cat. No. 5104 1 x 2.0 mL FOR IN-VITRO DIAGNOSTIC USE Gel Alkaline Phosphatase Isoenzyme Control 20mL 001831 Alkaline Phosphatase Isoenzyme Control is to be used as a…
Category
Medical Device
Distribution
Distributed nationwide