The Recall Desk

State

Northern Mariana Islands product recalls

73,388 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 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20976–21000 of 73411

  • ModerateFDA (Devices)·Z-0956-2022·2022-04-27

    Abbott TactiCath Ablation Catheter Disabled by Preprogrammed First-Use Date

    Abbott is recalling 2,134 TactiCath ablation catheters manufactured with a preprogrammed 'First Use Date' that disables the device. Affected devices with 37 specific lot numbers were distributed in the U.S. and 21 other countries.

    Product
    Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter, Bi-D, Curve D-F, Model A-TCSE-DF, Sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0948-2022·2022-04-27

    Baxter Syringe Tip Caps Recalled Due to Incorrect Labeling

    Baxter is recalling DISCPAC syringe tip caps that are mislabeled as self-righting when they do not possess this capability, risking improper use in medical procedures.

    Product
    Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, Yellow, REF H93866100, 100 slip tip caps/package.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0949-2022·2022-04-27

    Terumo Cardiovascular Procedure Kit Recall for Shipping Damage

    Terumo Cardiovascular Systems Corp is recalling two lots of cardiovascular procedure kits due to packaging damage that occurred during shipping. The recall affects 64 units distributed in California and Indiana.

    Product
    Cardiovascular Procedure Kit catalog # 76645 & 73806
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0773-2022·2022-04-27

    Diclofenac Sodium Topical Solution Recalled Due to Manufacturing Quality Deviations

    Preferred Pharmaceuticals, Inc. is recalling Diclofenac Sodium Topical Solution because the manufacturing firm discontinued its stability study program, a CGMP violation. All products within their expiration dates are affected.

    Product
    Diclofenac Sodium Topical Solution 1.5% w/w, Generic for Pennsaid, 150 ml bottle, Rx Only, Mfg: Sola Pharmaceutical, Preferred Pharmaceuticals, Inc., The Physicians Solutions, NDC 68788-7918-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0968-2022·2022-04-27

    X-ray Imaging System Cooling Failure May Cause Tube Overheating

    Siemens Artis zee ceiling X-ray systems may fail to cool the X-ray tube if the coolant level drops. The system will automatically block X-ray emissions and display warning messages to prevent equipment damage.

    Product
    Artis zee ceiling, Model Number 10094137
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0984-2022·2022-04-27

    Beckman Coulter IRISpec CA Control glucose measurement failures recalled

    Beckman Coulter is recalling IRISpec CA/CB/CC control kits due to failures in glucose measurement for the CA Control component. The recall affects laboratory quality control products distributed worldwide.

    Product
    Beckman Coulter IRISpec CA/CB/CC control, Catalog #800-7211, containing 3 x 100 mL bottles each of CA Control, CB Control, and CC Control.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0783-2022·2022-04-27

    FDA Recalls artnaturals Scent-Free Hand Sanitizer for Manufacturing Deviations

    artnaturals Scent-Free Hand Sanitizer is recalled due to manufacturing process deviations. Approximately 570,268 bottles distributed nationwide are affected.

    Product
    artnaturals hand sanitizer, SCENT FREE HAND SANITIZER (ethyl alcohol 62.5%), 8 fl oz (236 ml) bottles, Dist. By artnaturals, Gardena, CA 90248, UPC: 8 16820 02820 5
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0981-2022·2022-04-27

    Oral DNA Collection Device Recalled for Evaporating Stabilizing Liquid

    DNA Genotek Inc. is recalling ORAcollect Dx oral DNA collection devices because the stabilizing liquid can evaporate, reducing shelf life and potentially affecting sample preservation.

    Product
    ORAcollect Dx, Catalog Number/SKU: OCD-100, OCD-100A. Material numbers: OCD-100, OCD-100.008, OCD-100.012, OCD-100.014+ACP078, OCD-100.014+ACP078, OCD-100.032 and OCD-100A, OCD-100A.022, OCD-100A.023, OCD-100A.024, OCD-100A.025
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0980-2022·2022-04-27

    Artis Q.zen Biplane X-ray Systems Coolant Level Failure Recall

    Siemens is recalling 69 Artis Q.zen biplane systems where coolant levels may drop sufficiently to prevent adequate X-ray tube cooling, triggering automatic shutdown safeguards.

    Product
    Artis Q.zen biplane, Model Number 10848355
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0982-2022·2022-04-27

    Oral RNA Collection Kit Recalled Due to Stabilizer Evaporation

    DNA Genotek Inc. is recalling ORAcollect RNA: ORE-100 kits due to evaporation of the stabilizing liquid, which reduces shelf life. Approximately 17,080 units are affected, including lot YJ530.

    Product
    ORAcollect RNA: ORE-100
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V278000·2022-04-26

    Porsche Taycan seat wire harness defect may deactivate airbags

    Porsche is recalling certain 2020-2021 Taycan vehicles because the driver and passenger seat wire harness could become damaged during horizontal seat adjustment. A damaged harness may deactivate airbags, increasing crash injury risk.

    Product
    PORSCHE — PORSCHE TAYCAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·011-2022·2022-04-25

    Lakeside Refrigerated Services Recalls Ground Beef Due to E. coli O103 Risk

    Lakeside Refrigerated Services is recalling approximately 120,872 pounds of ground beef products due to possible E. coli O103 contamination. The products were shipped to retail locations nationwide.

    Product
    Lakeside Refrigerated Services Recalls Ground Beef Products Due to Possible E. coli O103 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V277000·2022-04-25

    PACCAR Recalls Kenworth and Peterbilt Trucks for Steering Fastener Defect

    PACCAR is recalling 2018-2020 Kenworth and Peterbilt trucks because steering arm fasteners may fail, potentially causing loss of steering control.

    Product
    KENWORTH — KENWORTH, PETERBILT T270, 579, T440, 567
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V276000·2022-04-25

    Gillig Recalls 2014-2021 Low Floor Buses Due to Engine Start Risk

    Gillig is recalling 2014-2021 Low Floor transit buses because rear-mounted ultracapacitors may allow the engine to start unexpectedly while the master battery disconnect switch is off.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V272000·2022-04-22

    Thomas Built Buses Recalling HDX Models for Battery Cable Fire Risk

    Daimler Trucks North America is recalling 2019-2023 Thomas Built Bus HDX commercial buses because an improperly routed battery cable may chafe and cause an electrical short circuit, increasing the risk of a fire.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V270000·2022-04-22

    2022 Alliance RV Paradigm Recreational Trailers Recalled for LP Gas Leak

    Alliance RV is recalling certain 2022 Paradigm, Avenue, and Valor recreational trailers due to cracked quick disconnect fittings in the LP gas system that can cause gas leaks, creating a fire hazard.

    Product
    ALLIANCE RV — ALLIANCE RV AVENUE, PARADIGM, VALOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V271000·2022-04-22

    Thomas Built Buses Recalls HDX School Buses for Fire Risk

    Daimler Trucks North America is recalling 2019-2023 Thomas Built Buses HDX school buses because a battery cable may chafe and cause a fire.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V273000·2022-04-22

    Tiffin Allegro motorhomes recalled for faulty hydraulic slide cylinders

    Tiffin is recalling certain 2021 and 2022 Allegro and Allegro Bay motorhomes due to defective hydraulic cylinder seals. The slide-room may extend unintentionally, increasing crash risk.

    Product
    TIFFIN — TIFFIN ALLEGRO, ALLEGRO BAY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·22125·2022-04-21

    Insignia Air Fryers and Air Fryer Ovens Recalled for Fire and Burn Hazards

    About 635,000 Insignia air fryers and air fryer ovens can overheat, posing fire and burn hazards. Best Buy is offering refunds or store credit for affected units sold between November 2018 and February 2022.

    Product
    Insignia Air Fryers and Air Fryer Ovens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22123·2022-04-21

    LUXE+WILLOW Heated Blankets Recalled Due to Fire and Burn Hazards

    MWA LLC is recalling about 4,200 LUXE+WILLOW heated blankets sold nationwide from January to March 2022 because the blanket can overheat if left plugged in and powered on for extended periods, creating fire and burn hazards.

    Product
    LUXE+WILLOW Heated Blankets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22124·2022-04-21

    Children's Pajamas Recalled Due to Flammability Hazard

    The Red League is recalling approximately 910 children's pajamas that fail to meet federal flammability standards for sleepwear, posing a risk of burn injuries. Consumers should remove the pajamas from children and contact The Red League for return instructions and a full refund.

    Product
    Children's pajamas
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22742·2022-04-21

    Overhead Garage Storage Racks Recalled for Impact Injury Hazard

    SafeRacks/Monsterrax overhead garage storage racks may collapse from the ceiling due to defective hex bolts, posing an impact injury hazard. About 12,800 units sold online from September through December 2021.

    Product
    Overhead Garage Storage Racks
    Category
    Consumer Product
    Distribution
    Distributed nationwide