The Recall Desk

State

Northern Mariana Islands product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32926–32950 of 73745

  • SevereFDA (Food)·F-1561-2019·2019-07-24

    ADM Recalls Baker's Corner Flour Due to Potential E. coli O26 Presence

    ADM is recalling Baker's Corner All Purpose Flour because of the potential presence of E. coli O26. The product was sold at ALDI stores in 11 states.

    Product
    Baker's Corner All Purpose Flour 5 lb. bag UPC code: 041498130404
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1575-2019·2019-07-24

    ADM Recalls Flour Products Due to Potential E. coli O26 Presence

    ADM is recalling specific lots of flour products due to the potential presence of E. coli O26. The affected products were distributed to retailers and commercial bakeries in multiple states.

    Product
    Commander Flour Enr, Mt Bulk Product Code 704020
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1564-2019·2019-07-24

    Recall of Pillsbury Hi Gluten Flour due to E. coli risk

    ADM is recalling Pillsbury Hi Gluten Flour because of potential E. coli O26 contamination. The affected flour was distributed to food service in New York and Pennsylvania.

    Product
    Pillsbury BALANCER HI GLUTEN FLOUR BLEACHED BROMATED ENRICHED 50 LB bag
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1941-2019·2019-07-24

    Datascope CS100 Intra-Aortic Balloon Pump Recalled for Battery Maintenance Issues

    Datascope Corp. is recalling CS100 Intra-Aortic Balloon Pumps because improper battery maintenance may result in less than minimum run time. Revised labeling and training are being offered.

    Product
    CS100 Intra-Aortic Balloon Pump, English, 110V; 0998-00-3013-53 For cardiovascular use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1939-2019·2019-07-24

    Datascope Cardiosave Hybrid Intra-Aortic Balloon Pump Recalled for Labeling Defects

    Datascope Corp. is recalling 6,197 Cardiosave Hybrid Intra-Aortic Balloon Pumps worldwide due to inadequate labeling regarding battery maintenance.

    Product
    Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP), 0998-00-0800-53 For cardiovascular use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1578-2019·2019-07-24

    ADM Recalls Bulk Flour Due to Potential E. coli O26 Presence

    ADM is recalling bulk flour products due to the potential presence of E. coli O26. The affected flour was distributed to retailers and commercial bakeries in multiple states.

    Product
    Springup Flr Enr, Mt Bulk Flour Product Code 703020
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·19172·2019-07-24

    Porter-Cable Table Saws Recalled by CPSC Due to Fire Hazard

    Chang Type is recalling Porter-Cable 10-inch table saws sold at Lowe's because the motors can overheat and cause fires. No injuries have been reported.

    Product
    Porter-Cable 10" Table Saws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1944-2019·2019-07-24

    Datascope CS300 Intra-Aortic Balloon Pump Recalled for Battery Maintenance Issues

    Datascope Corp. is recalling CS300 Intra-Aortic Balloon Pumps because improper battery maintenance may result in less than the minimum required operating power.

    Product
    CS300 Intra-Aortic Balloon Pump, English, 220V; 0998-00-3023-55 For cardiovascular use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1572-2019·2019-07-24

    ADM Recalls Latina Niagra Flour Due to Potential E. coli O26 Presence

    ADM is recalling specific lots of Latina Niagra Flour due to the potential presence of E. coli O26. Consumers should check their pantry for the affected product code and lot number.

    Product
    Latina Niagra Flour 50lbs bags Product Code 845202 Lot#: 8344BF
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1573-2019·2019-07-24

    ADM Recalls Dominator Flour Due to Potential E. coli O26 Presence

    ADM is recalling specific lots of Dominator Flour because of the potential presence of E. coli O26. The product was distributed in New York and Pennsylvania.

    Product
    Dominator Flour 50lb bags Product Code 745220 Lot#: 8319BF
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1567-2019·2019-07-24

    ADM Recalls Multiple Flour Brands Due to Potential E. coli O26 Presence

    ADM is recalling various flour products, including King Arthur and Pillsbury brands, due to the potential presence of E. coli O26.

    Product
    King Arthur All Purpose Flour 5 LB bag UPC code: 071012010509
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1983-2019·2019-07-24

    Olympus Mobile Workstations Recalled for Potential Instability

    Olympus is recalling WM-NP2 and WM-DP2 mobile workstations because the control panel arm may cause the unit to fall over if a heavy monitor is attached.

    Product
    Olympus WM-NP2 or WM-DP2 Mobile Workstations with Nurse Control Panel Arm, Model. No. MAJ-1664
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·19173·2019-07-24

    Trek Recalls Kickster Bikes Due to Broken Steer Tube Clamp Hazard

    Trek is recalling Kickster balance bikes because the steer tube clamp can break, posing a fall hazard to children. Consumers should take bikes to a retailer for a free repair.

    Product
    Trek Kickster
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1951-2019·2019-07-24

    GE Healthcare Recalls Revolution CT Scanners Due to Radiation Exposure

    GE Healthcare is recalling Revolution CT scanners because they may expose patients to additional low-dose radiation.

    Product
    Revolution CT scanners Product Usage: The system is intended for head, whole body, cardiac and vascular X-ray Computed Tomography applications.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V545000·2019-07-24

    Mercedes-Benz Metris Recalled for Incorrect Operator's Manual

    Daimler Vans USA is recalling 2019 Mercedes-Benz Metris vehicles because the printed operator's manual may not match the vehicle's features, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V549000·2019-07-24

    Thomas Built Buses Recall Roof Escape Hatch Handle Defect

    Daimler Trucks North America is recalling specific Thomas Built Buses because the roof escape hatch handle may break, preventing emergency exit.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2, SAF-T-LINER HDX, MINOTOUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1960-2019·2019-07-24

    Zimmer Biomet Recalls Reverse Shoulder Instrument Cases Due to Sterilization Validation

    Zimmer Biomet is recalling 92 Comprehensive Reverse Shoulder Instrument Cases because they lack adequate sterilization validation. The products were distributed in the US and 16 foreign countries.

    Product
    Comprehensive Reverse Shoulder Instrument Case Outer (Outer Case Vault Only), Item Number 595509
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1961-2019·2019-07-24

    Zimmer Biomet Recalls Reverse Shoulder Instrument Cases Due to Sterilization Validation

    Zimmer Biomet is recalling 1,257 Comprehensive Reverse Shoulder Instrument Cases because they lack adequate sterilization validation. The products were distributed in the US and 16 foreign countries.

    Product
    Comprehensive Reverse Shoulder Instrument Case Total (Outer Case Vault Only), Item Number 595510
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1986-2019·2019-07-24

    Clariance Erisma-LP Posterior Fixation System Recalled for Screw Disassembly Risk

    Clariance Inc is recalling Erisma-LP posterior fixation system components due to a potential for polyaxial screws to disassemble during implantation.

    Product
    Erisma- LP posterior fixation system with the below specifically affected products: 1. Erisma-LP polyaxial screws - 4.5, 5.5, 6.5, 7.5, 8.5, 9.5, 105 mm (all lengths); 2. Erisma-LP Screwdriver; 3. Erisma-LP T20 Wrench; 4. Erisma-LPT20 Snap Fit Tightening…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1971-2019·2019-07-24

    Electrode Conductivity Spray Solution Recalled for Antimicrobial Testing Failures

    Pharmaceutical Innovations, Inc. is recalling ElectroMist Electrode Conductivity Spray Solution due to potential failures in stability antimicrobial effectiveness testing.

    Product
    ElectroMist product codes: 36-3310-04 - Product Usage: Electrode Conductivity Spray Solution.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1972-2019·2019-07-24

    Pharmaceutical Innovations Recalls Alpha Conducting Solution Due to Stability Testing Concerns

    Pharmaceutical Innovations, Inc. is recalling Alpha Conducting solution due to potential failures in stability antimicrobial effectiveness testing. The product was distributed in the US and internationally.

    Product
    Alpha Conducting solution product codes: 3310-25 ASCR - Product Usage: Electrode Conductivity Spray Solution.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V542000·2019-07-24

    Forest River Recalls 2019 Glaval and Startrans Buses for Seat Belt Bolt Issue

    Forest River is recalling 2019 Glaval and Startrans buses because driver's seat belt anchor bolts may not be fully tightened, potentially causing the seat belt to fail in a crash.

    Product
    GLAVAL BUS — GLAVAL BUS, STARTRANS LEGACY, ENTOURAGE, UNIVERSAL, MFSAB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V547000·2019-07-24

    Audi Recalls Vehicles Due to Passenger Air Bag Disabling Risk

    Audi is recalling 2017-2019 models because cable oxidation may disable the passenger air bag, increasing injury risk in a crash.

    Product
    AUDI — AUDI A5, A4 ALLROAD, RS 5, S5 CABRIOLET
    Category
    Vehicle
    Distribution
    Distributed nationwide