The Recall Desk

State

Northern Mariana Islands product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

52451–52475 of 73847

  • SevereFDA (Devices)·Z-2362-2015·2015-08-26

    CareFusion Alaris Syringe Pump Recall for Unresponsive Control Defect

    CareFusion 303, Inc. is recalling Alaris Syringe Pumps, Model 8110, because they may become unresponsive to key presses after a channel error is cleared.

    Product
    Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housing Assembly Service, Part No. 49000226, and Lower Housing/Carriage Block Assembly, Part No. 148188-100.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2369-2015·2015-08-26

    Teleflex Sheridan SHER-I Bronch Accessory Pack Recalled for Connector Defect

    Teleflex Medical is recalling Sheridan SHER-I Bronch Accessory Packs because the double swivel connector may crack or separate on the endobronchial tube.

    Product
    HUDSON RCI, Sheridan SHER-I BRONCH Accessory Pack, Rx Only, Sterile. Used to aspirate liquids or semisolids from a patient's upper airway.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1332-2015·2015-08-26

    Mylan Recalls Gemcitabine Injection Vials Due to Particulate Matter

    Mylan Institutional LLC is recalling specific lots of Gemcitabine for Injection due to the presence of particulate matter. The affected vials were distributed nationwide and in Puerto Rico.

    Product
    Gemcitabine for Injection, USP, 200 mg*/vial, Lyophilized powder in a Single-Use Vial, Rx only, labeled as a) Manufactured for: Mylan Institutional LLC, Rockford, IL 61103, Made in India, NDC 67457-464-20, UPC 3 67457 46420 6; and b) Distributed by Pfizer Labs, Division of…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2368-2015·2015-08-26

    Teleflex Recalls Sheridan Sher-I-BRONCH Endobronchial Tubes Due to Connector Cracking

    Teleflex Medical is recalling Sheridan Sher-I-BRONCH endobronchial tubes because the double swivel connector may crack or separate.

    Product
    HUDSON RCI, Sheridan Sher-I-BRONCH, Endobronchial Tube (Right sided), Sizes: 28 Fr., 35 Fr., 37 Fr., 39 Fr. and 41 Fr., Rx Only, Sterile. Intended for use in thoracic surgery, bronchospirometry, for the administration of bronchial anesthesia and other uses commonly requiring…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2433-2015·2015-08-26

    Medline Electrical Surgical Clippers Recalled for Overheating Charging Base

    Medline is recalling 7,602 electrical surgical clippers because the charging base can overheat and smoke. The units were distributed in the U.S. and eight other countries.

    Product
    Medline Electrical Clipper with Charging base The Electrical Surgical Clipper is intended for the removal of body hair from patients as required prior to surgery or other minor procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1349-2015·2015-08-26

    Bausch & Lomb Recalls Bromfenac Ophthalmic Solution Due to Sterility Concerns

    Bausch & Lomb is recalling 13,995 bottles of Bromfenac Ophthalmic Solution, 0.09%, because preservative testing failed, raising concerns about sterility.

    Product
    Bromfenac Ophthalmic Solution, 0.09%, 1.7 mL Bottle, Rx Only. Manufactured by Bausch & Lomb Incorporated Tampa, FL 33637. NDC: 24208-439-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1331-2015·2015-08-26

    Mylan Recalls Carboplatin Injection Due to Particulate Matter

    Mylan Institutional LLC is recalling Carboplatin Injection 450 mg/45 mL due to the presence of particulate matter.

    Product
    CARBOplatin Injection 450 mg/45 mL (10 mg/mL), 45 mL packaged in a 100 mL Multi-Dose Vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103, Made in India, NDC 67457-493-46, UPC 3 67457 49346 6.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2370-2015·2015-08-26

    Teleflex Medical Recalls Sheridan Double Swivel Connectors Due to Cracking Risk

    Teleflex Medical is recalling Sheridan double swivel connectors because they may crack or separate on endobronchial tubes.

    Product
    HUDSON RCI, Sheridan, SHER-I-SWIV and SHER-I-SWIV/FO Double Swivel, Rx Only, Sterile. Used temporarily to make rigid a flexible tracheal tube to aid its insertion into a patient.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V541000·2015-08-26

    FCA Recalls 2013-2014 Ram Trucks Due to Track Bar Weld Defect

    FCA is recalling 2013-2014 Ram 2500 and 3500 trucks because inadequate welds may cause front track bar brackets to separate, increasing crash risk.

    Product
    RAM — RAM 3500, 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1330-2015·2015-08-26

    PYROLA Advanced Joint Formula Recalled for Undeclared Prescription Drugs

    GC Natural Nutrition is recalling PYROLA Advanced Joint Formula capsules because they contain undeclared prescription and over-the-counter drugs.

    Product
    PYROLA Advanced Joint Formula capsules, 60-count bottle, G & C Natural Nutrition Inc., Fullerton, CA 92833, UPC 7 11746 00075 8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·15227·2015-08-26

    Bosch Recalls Dremel Rotary Tools Due to Overheating and Burn Risk

    Robert Bosch Tool is recalling Dremel MICRO Model 8050 rotary tools because the circuit board can overheat, melt the enclosure, and cause burns.

    Product
    Dremel® MICRO™ Model 8050 Rotary Tool
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2394-2015·2015-08-26

    Winco Care Cliner Chairs Recalled for Non-Fire-Retardant Foam

    Winco Mfg. is recalling four Care Cliner X-Large chairs because the foam used was standard foam rather than fire-retardant foam.

    Product
    Winco Care Cliner X-Large - with Steel Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2393-2015·2015-08-26

    Winco Care Cliner X-Large Chair Recalled for Fire Retardant Foam Mislabeling

    Winco Mfg., LLC is recalling Care Cliner X-Large chairs because the foam was mislabeled as fire retardant but is actually standard foam.

    Product
    Winco Care Cliner X-Large - with Nylon Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2391-2015·2015-08-26

    Winco XL Convalescent Recliner Recalled for Fire Safety Defect

    Winco Mfg. is recalling XL Convalescent Recliners because the foam used was not fire retardant as required.

    Product
    Winco XL Convalescent Recliner - with Steel Casters Long term patient recliner (Nursing, Rehabilitation, Geriatric Home Use, Retirement facilities)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2392-2015·2015-08-26

    Winco Care Cliner Standart Steel Casters Recalled for Fire Hazard

    Winco Mfg., LLC is recalling Care Cliner Standart chairs because the foam used was not fire retardant as required.

    Product
    Winco Care Cliner Standart - Steel Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2400-2015·2015-08-26

    Winco Elite Care Chairs Recalled for Fire Retardant Foam Mislabeling

    Winco Mfg. is recalling 32 Elite Care chairs because foam shipped as fire retardant was actually standard foam, failing safety standards.

    Product
    Winco Elite Care Cliner w/Swing Away Arms Standard - with Nylon Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2397-2015·2015-08-26

    Winco Drop Arm Care Cliner Chairs Recalled for Fire Hazard

    Winco Mfg. is recalling three Drop Arm Care Cliner chairs because the foam used was not fire retardant as required.

    Product
    Winco Drop Arm Care Cliner X-Large - with Nylon Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2398-2015·2015-08-26

    Winco Designer Care Cliner chairs recalled for non-compliant foam

    Winco Mfg., LLC is recalling two Designer Care Cliner chairs because the foam used was not fire retardant as required.

    Product
    Winco Designer Care Cliner - with Nylon Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2403-2015·2015-08-26

    Winco Patient Recliner Recalled for Non-Fire-Retardant Foam

    Winco Mfg. is recalling specific patient recliners because the foam used was standard foam rather than fire-retardant foam, failing to meet safety standards.

    Product
    Winco Nocturnal Elite Care Cliner - with Nylon Casters Lay Flat Clinical Patient Recliner w/ Trendelenburg (Long Term Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2390-2015·2015-08-26

    Sedecal RadPro 40kW Digital X-Ray Panel Recalled for Uncontrolled Movement Risk

    Sedecal S.A. is recalling RadPro 40kW Digital X-Ray systems because electrostatic energy may cause uncontrolled movements that could bump into users or patients.

    Product
    RadPro 40kW Digital X-Ray Panel and Mobile/Portable Diagnostic X-Ray. Intended for use by a qualified/trained doctor or technician on both adult and pediatric subjects for taking diagnostic radiographic exposures of the skull, spinal column, chest, abdomen, extremities, and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15226·2015-08-26

    CAMP USA Recalls Tour Nanotech Crampons Due to Fall Hazard

    CAMP USA is recalling Tour Nanotech Automatic and Semi-Automatic crampons because the heel bail can detach, posing a fall hazard. No injuries have been reported.

    Product
    Tour Nanotech Automatic and Semi-Automatic Crampons
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2395-2015·2015-08-26

    Winco Drop Arm Care Cliner Chairs Recalled for Fire Hazard

    Winco Mfg. is recalling 30 Drop Arm Care Cliner chairs because the foam used was not fire retardant as required.

    Product
    Winco Drop Arm Care Cliner Standard - with Nylon Casters Oncology, Dialysis, Hospital Recovery, Home Dialysis Use, Physician Facilities.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2423-2015·2015-08-26

    International Biophysics Recalls IBC Aortic Punch Due to Seal Issues

    International Biophysics Corp. is recalling 10,330 units of IBC Aortic Punch because the heat seal on sterile pouches may not meet strength acceptance criteria.

    Product
    IBC Aortic Punch Catalog Numbers APM40, APL48A, APM44A, APL40A, APM40A, CVAPL36, CVAPL40, CVAPL44, CVAPL48, CVAPL52, APM28BM, APM36BM, APM40BM, APM44BM, APM48BM, APM40BK, APM48BK, APM36BK, APM44BK, APM28, APM36, APL44, APM40 Product Usage: The IBC Aortic Punch is a…
    Category
    Medical Device
    Distribution
    Distributed nationwide