State

Northern Mariana Islands product recalls

73,509 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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25676–25700 of 73532

SevereFDA (Drugs)·D-0284-2021·2021-03-03
Teva Recalls MethyIPREDNISolone Acetate Injectable Suspension Due to Sterility Concerns
Teva Pharmaceuticals is recalling 15,043 vials of MethyIPREDNISolone Acetate Injectable Suspension because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Product
MethyIPREDNISolone Acetate Injectable Suspension USP, 400 mg/5 mL (80 mg/mL), 5 mL Multiple-Dose Vial, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-0063-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0274-2021·2021-03-03
Teva Recalls Epoprostenol Sodium Injection Due to Sterility Concerns
Teva Pharmaceuticals is recalling Epoprostenol Sodium for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Product
Epoprostenol Sodium for Injection, 0.5 mg/vial (500,000 ng), 1X10ML vial, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-1985-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0273-2021·2021-03-03
Teva Recalls Sterile Diluent for Epoprostenol Sodium Due to Sterility Concerns
Teva Pharmaceuticals is recalling specific lots of Sterile Diluent for Epoprostenol Sodium for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Product
Sterile Diluent for Epoprostenol Sodium for Injection, 50 mL vial (NDC 0703-9258-01), packaged in 2X50ML per tray (NDC 0703-9258-09), Rx only, TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0278-2021·2021-03-03
Teva Recalls Toposar Etoposide Injection Due to Sterility Assurance Issues
Teva Pharmaceuticals is recalling Toposar (etoposide) injection vials because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Product
Toposar (etoposide injection USP), 1 gram/50 mL (20 mg/mL), 50 mL Multiple-dose Vial, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-5657-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0282-2021·2021-03-03
Teva Recalls MethyIPREDNISolone Acetate Injectable Suspension Due to Sterility Concerns
Teva Pharmaceuticals is recalling specific lots of MethyIPREDNISolone Acetate Injectable Suspension because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Product
MethyIPREDNISolone Acetate Injectable Suspension USP, 400 mg/10 mL (40 mg/mL), 10 mL Multiple-Dose Vial, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-0045-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0280-2021·2021-03-03
Teva Recalls Epoprostenol Sodium Injection Due to Sterility Concerns
Teva Pharmaceuticals is recalling Epoprostenol Sodium for Injection because manufacturing areas exceeded microbial acceptance levels, compromising sterility assurance.
Product
Epoprostenol Sodium for Injection, 1.5 mg/vial (1,500,000 ng), 10 mL vial, Rx only, Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 0703-1995-01.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0271-2021·2021-03-03
Teva Recalls Dacarbazine Injection Due to Sterility Assurance Concerns
Teva Pharmaceuticals is recalling Dacarbazine for Injection USP because manufacturing areas exceeded microbial recovery levels, compromising sterility assurance.
Product
Dacarbazine for Injection USP, 200 mg, Single Use Vial (NDC 0703-5075-01), packaged in 10X20 ML Single Use Vials per tray (NDC 0703-5075-03); Rx only, TEVA Pharmaceuticals USA, INC., North Wales, PA 19454.
Category
Drug
Distribution
Distributed nationwide
HighCPSC·21090·2021-03-03
Haro Recalls Masi Bicycles Due to Fork Steerer Tube Breakage Hazard
Haro Bicycles is recalling approximately 510 Masi Evoluzione and Gran Corsa bicycles from model years 2017-2020 because the fork steerer tube can break, causing riders to lose control and fall.
Product
Model Year 2017-2020 Masi Evoluzione and Gran Corsa bicycles
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1136-2021·2021-03-03
Ortho-Clinical Recalls Deformed VITROS Chemistry VersaTips
Ortho-Clinical Diagnostics is recalling deformed VITROS Chemistry VersaTips that may cause assay results to be biased by up to +/-16%.
Product
VITROS Chemistry Products VersaTips - Product Usage: used to dispense samples to MicroSlide assays and sample and reagent fluid for MicroWell assays. In addition, VersaTips are used to dispense R1 Reagent Fluid into cuvettes in combination with sample fluid for Micro Tips…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1147-2021·2021-03-03
Northgate Recalls ConMed Abdominal Insufflators Due to Incorrect Tubing Material
Northgate Technologies is recalling 25 ConMed 50L abdominal insufflators because an internal tubing component was made with untested material.
Product
ConMed 50L abdominal insufflator, Catalog Number 72-00258-0 / GS2000 - Product Usage: The device will maintain an expanded cavity (pneumoperitoneum) to allow the insertion of a variety of surgical instruments through the abdominal wall for visual examination of the interior or…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V133000·2021-03-03
Altec Recalls 2017-2019 Wood Chippers Due to Exhaust Leak Fire Risk
Altec is recalling 2017-2019 DC1317 and DRM12 wood chippers because a flexible exhaust pipe section may separate, creating an exhaust gas leak that increases the risk of a fire.
Product
ALTEC — ALTEC DC1317 CHIPPER, DRM12 WOOD CHIPPER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1143-2021·2021-03-03
Natus EDS 3 CSF External Drainage System Recalled for Pyrogen Test Failure
Natus Manufacturing Limited is recalling 7 units of the EDS 3 CSF External Drainage System because the device failed to meet pyrogen test requirements for endotoxins.
Product
Ref: NT821731C, Natus EDS 3 CSF External Drainage System - Product Usage: indicated for draining cerebrospinal fluid (CFS) from the cerebral ventricles or the lumbar subarachnoid space as a means of reducing intracranial pressure and CSF volume when the insertion of a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1137-2021·2021-03-03
Respironics Recalls 94 Philips Ventilator Batteries Due to Design Verification Issues
Respironics is recalling 94 Philips V60 ventilator batteries because they were shipped without proper design verification. The recall covers distribution across multiple U.S. states.
Product
PHILIPS BATTERY, V60 14.4V, 11.0 Ah, 163 Wh, REF 1076374(1058272), LOT M94663-P1 - Product Usage: The ventilator is intended to be used only with various combinations of Respironics-recommended patient circuits, interfaces (masks), humidifiers, and other accessories.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1145-2021·2021-03-03
Smiths Medical Recalls Bivona Cuffless FlexTend Tracheostomy Tubes Due to Packaging Error
Smiths Medical is recalling specific lots of Bivona Cuffless FlexTend Tracheostomy Tubes because they may have been packaged with the wrong neck flange, posing a risk of patient injury.
Product
Tube Tracheostomy and Tube Cuff, Bivona¿ Cuffless Neonatal/Pediatric FlexTend" Tracheostomy Tube (model 60PFS45, lots 3991171, 3991172, and 3988103) V Neck Flange 4.5mm - Product Usage: intended to provide direct airway access for a tracheotomized patient for up to 29 days. It…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V135000·2021-03-03
Nissan Recalls 2016-2019 Sentra Vehicles for Brake Light Switch Defect
Nissan is recalling 2016-2019 Sentra vehicles because a contaminated brake light switch may prevent brake lights from illuminating, increasing crash risk.
Product
NISSAN — NISSAN SENTRA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1142-2021·2021-03-03
Recall of Parietex Hydrophilic Anatomical Mesh Due to Incorrect Side Labeling
Covidien is recalling Parietex hydrophilic anatomical mesh where the package label indicates left-side use but contains a right-side device. This labeling error can lead to implant failure and hernia recurrence.
Product
Covidien Parietex hydrophilic anatomical mesh 15 cm x 10 cm polyester left - Product Usage: designed for the repair of inguinal hernias via laparoscopic or posterior open procedures Item Code: TECT1510AL
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V132000·2021-03-03
2021 Volkswagen Atlas Wheels May Separate Due to Machining Defect
Volkswagen is recalling certain 2021 Atlas and Atlas Cross Sport vehicles due to improperly machined wheel lug bolt holes that may prevent wheels from attaching properly, risking wheel separation and crashes.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1148-2021·2021-03-03
Northgate Recalls Steris CO2MPACT Endoscopic Insufflator Systems Due to Tubing Material Error
Northgate Technologies is recalling 45 Steris CO2MPACT Endoscopic Insufflator systems because an internal tubing component was made with incorrect, untested material.
Product
Steris CO2MPACT Endoscopic Insufflator system, Catalog Number 72-00310-0 / 710300 - Product Usage: designed to use CO2 as a distention media in the gastrointestinal tract when used in conjunction with a gastrointestinal endoscope.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1141-2021·2021-03-03
Ecolab Recalls Slush and Warmer Disc Drapes Due to Sterile Barrier Risk
Ecolab is recalling specific lots of ORS-320 Slush + Warmer Disc Drapes because manufacturing slits may breach the sterile barrier, posing an infection risk to patients.
Product
Slush + Warmer Disc Drape; Model ORS-320 Slush + Warmer Disc Drapes - Product Usage: single-use equipment cover intended for use during various surgeries where warm irrigation, slush and/or cold solution is required.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0287-2021·2021-03-03
Dr. Reddy's Recalls Imatinib Mesylate Tablets for Dissolution Failures
Dr. Reddy's Laboratories is recalling specific lots of Imatinib Mesylate 100mg tablets because they failed to meet required dissolution specifications.
Product
IMATINIB — IMATINIB (IMATINIB)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0270-2021·2021-03-03
Areva Pharmaceuticals Recalls Irinotecan Hydrochloride Injection Due to CGMP Deviations
Areva Pharmaceuticals is recalling 3,287 vials of Irinotecan Hydrochloride Injection due to manufacturing quality deviations identified in a Warning Letter.
Product
Irinotecan Hydrochloride Injection, USP, 40 mg/2 mL (20 mg/mL), 2 mL Single-Dose Vial, Rx Only, Distributed by: Areva Pharmaceuticals, Inc., Gerogetown, IN 47122, Made in India, NDC 59923-714-02.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1144-2021·2021-03-03
Siemens ARTIS Icono Biplane and Floor Systems Recalled for Software Errors
Siemens is recalling 41 ARTIS Icono systems with software version VE20B due to misleading error messages and manual gaps that may cause procedure termination.
Product
ARTIS Icono biplane Model:11327600 ARTIS Icono floor system Model: 11327700 with software version VE20B - Product Usage: Intended for single and biplane diagnostic imaging and interventional procedures.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1135-2021·2021-03-03
Medline Recalls STAT-Site B-HB Controls Due to Shipment Compromise
Medline Industries is recalling specific lots of STAT-Site B-HB controls because the products were compromised during shipment. The recall affects 46 units distributed in Mississippi, Ohio, and Illinois.
Product
S-O303000 CONTROL, STAT-SITE B-HB, 2X3ML,1LOW,1HIGH - Product Usage: intended for the quantitative determination of the ketone body ¿-Hydroxybutyrate in serum or plasma. For laboratory use only.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·21V130000·2021-03-02
Ferrara Recalls 2009-2020 Aerial Vehicles Due to Trolley Defect
Ferrara is recalling 2009-2020 Aerial vehicles because a defective waterway trolley can detach and fall, posing a risk of injury or death.
Product
FERRARA — FERRARA AERIAL
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V128000·2021-03-02
Forest River Recalls 2021 Coachmen Catalina Travel Trailers for Slide-Room Defect
Forest River is recalling 2021 Coachmen Catalina 184BHS and 184 BHS-W travel trailers because incorrectly installed interior plates may cause the slide-room to partially detach during transit.
Product
COACHMEN — COACHMEN CATALINA
Category
Vehicle
Distribution
Distributed nationwide