The Recall Desk

State

Northern Mariana Islands product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44276–44300 of 73832

  • ModerateFDA (Devices)·Z-1250-2017·2017-03-01

    Vascular Solutions Recalls GrebSet Micro-Introducer Kits Due to Shelf Life Discrepancy

    Vascular Solutions is recalling 633 units of GrebSet Micro-Introducer Kits because the guidewires have a shorter shelf life than the kit expiration date.

    Product
    GrebSet Micro-Introducer Kit, model 7941, Sterilized with Ethylene Oxide. Product Usage: The GrebSet micro-introducer kit is intended to facilitate the percutaneous placement of guidewires in the vascular system and for delivery of contrast media to vascular sites.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1230-2017·2017-03-01

    Cardiovascular Systems Recalls Mislabelled Diamondback 360 Peripheral Atherectomy Components

    Cardiovascular Systems Inc is recalling 8 units of the Diamondback 360 Peripheral 1.50 Classic system because a 1.50mm Solid Crown OAD was mislabeled as a 1.50mm Crown OED.

    Product
    DIAMONDBACK 360 Peripheral 1.50 Classic, Model DBP-150CLASS145 Peripheral Orbital Atherectomy System (OAS) is a minimally invasive, catheter-based OAS designed for improving luminal diameter in patients with peripheral arterial disease (PAD). PAD is caused by the accumulation…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1249-2017·2017-03-01

    Durex Condoms Recalled for Missing Benzocaine Labeling Information

    Reckitt Benckiser LLC is recalling Durex Pleasure Pack condoms because the package labeling is missing information about the active ingredient Benzocaine.

    Product
    Durex Pleasure Pack . 3 ultra fine lubricated latex condoms 12 ultra fine lubricated latex condoms 24 Ra fine lubricated latex condoms 3 ct UPC 3-02340-30042-04-1 3 ct - Walmart UPC 02340-70042-04 12ct - UPC 3-02340-30274-08-6 24 ct - UPC 302340-302190-04…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1239-2017·2017-03-01

    Smith & Nephew Dyonics Saw Blade Recall for Missing Expiration Date

    Smith & Nephew is recalling 2,646 Dyonics Saw Blades because they are provided sterile but lack an expiration date on the label.

    Product
    Smith & Nephew Dyonics Saw Blade, Standard, Product Number 3701
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1244-2017·2017-03-01

    Smith & Nephew Dyonics Saw Blade Recall Due to Missing Expiration Date

    Smith & Nephew is recalling 1,410 Dyonics Saw Blades because the single-use sterile devices lack expiration dates on the label.

    Product
    Smith & Nephew Dyonics Saw Blade, Long, Special, Product Number 3706
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1242-2017·2017-03-01

    Smith & Nephew Recalls Dyonics Saw Blades Due to Missing Expiration Dates

    Smith & Nephew is recalling 8,748 Dyonics Saw Blades because the single-use sterile devices lack expiration dates on their labels.

    Product
    Smith & Nephew Dyonics Saw Blade, Short, Narrow, Product Number 3704
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1246-2017·2017-03-01

    Merge Eye Station Import Utility Recalled for Image Import Errors

    Merge Healthcare is recalling the Eye Station Import Utility because images were not importing properly and were imported under "unknown" due to a validation issue.

    Product
    Merge Eye Station Import Utility (ESIU) when used with Merge Eye Station and Merge Eye Care PACS. The firm name on the labeling is Merge Healthcare, Hartland, WI.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1227-2017·2017-03-01

    Siemens N Latex HCY Reagent Recalled for Stability Issues

    Siemens Healthcare Diagnostics is recalling N Latex HCY Reagent kits due to reduced stability that may cause inaccurate homocysteine test results.

    Product
    N Latex HCY REAGENT, REF/Catalog OPAX03 /SMN 10445973 , IVD Product Usage: In-vitro diagnostic reagents for the quantitative determination of total homocysteine (HCY) in human serum, heparinized plasma and EDTA plasma by means of particle-enhanced immunonephelometry with…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1231-2017·2017-03-01

    Quidel Recalls Influenza Transport Swab Packages Due to Incorrect Swabs

    Quidel Corporation is recalling Influenza Transport Swab Packages because they may contain incorrect sample swabs mixed with the proper ones.

    Product
    Influenza Transport Swab Packages, Reference #20171, One lot with 1010 packages (each package contains 25 transport tubes). The Influenza Swabs in dry transport tubes are intended for use with influenza tests
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1240-2017·2017-03-01

    Smith & Nephew Dyonics Saw Blade Recall for Missing Expiration Date

    Smith & Nephew is recalling Dyonics Saw Blades because they are provided sterile but lack an expiration date on the label.

    Product
    Smith & Nephew Dyonics Saw Blade, Standard, Thick, Product Number 3702
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1243-2017·2017-03-01

    Smith & Nephew Dyonics Saw Blade Recall for Missing Expiration Date

    Smith & Nephew is recalling 3,462 Dyonics Saw Blades, Narrow (Product Number 3705) because the single-use sterile devices lack an expiration date on the label.

    Product
    Smith & Nephew Dyonics Saw Blade, Narrow, Product Number 3705
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1241-2017·2017-03-01

    Smith & Nephew Recalls Dyonics Saw Blades Due to Missing Expiration Dates

    Smith & Nephew is recalling 4,500 Dyonics Saw Blades, Short (Product Number 3703) because the single-use sterile devices lack expiration dates on their labels.

    Product
    Smith & Nephew Dyonics Saw Blade, Short, Product Number 3703
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0489-2017·2017-03-01

    Sage Q Care Continue Care Kit Recalled for Incorrect Expiration Date

    Sage Products Inc is recalling 640 Q Care Continue Care Kits because the kit's printed expiration date is incorrect. The kits contain oral care products with an earlier expiration date than printed on the main kit.

    Product
    Q Care Continue Care Kit for the non-ventilated patient; kit contains 1 Covered Yankauer, 2 Suction Toothbrush packages with Corinz (cetylpyridinium chloride) Antiseptic Cleansing and Moisturizing Oral Rinse, and 2 Suction Oral Swab packages with Corinz (cetylpyridinium…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1237-2017·2017-03-01

    Hidrex USA DVP1000 Recalled Due to Documentation Requirements

    Hidrex GmbH is recalling 180 units of the Hidrex USA DVP1000 device because it was reclassified from Class III to Class II, triggering new documentation requirements.

    Product
    Hidrex USA DVP1000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1236-2017·2017-03-01

    Hidrex USA DP450 Medical Device Recalled for Documentation Requirements

    Hidrex GmbH is recalling 64 units of the Hidrex USA DP450 device because it was reclassified from Class III to Class II, triggering new documentation requirements.

    Product
    Hidrex USA DP450
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1238-2017·2017-03-01

    Hidrex Recalls Daavlin Aquex Devices Due to Documentation Requirements

    Hidrex GmbH is recalling 250 Daavlin Aquex (DAAV1000) devices nationwide because the device was reclassified from Class III to Class II, triggering new documentation requirements.

    Product
    Daavlin Aquex (DAAV1000)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·17098·2017-02-28

    S.R. Smith Recalls Helix Pool Slides Due to Fall Hazard

    S.R. Smith is recalling Helix pool slides because children can fall off the side before reaching the pool, posing a risk of serious injury.

    Product
    Helix pool slides
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·17099·2017-02-28

    Dillard's Recalls Baby Faux-Fur Coats Due to Choking Hazard

    Dillard's is recalling about 1,800 baby faux-fur coats because metal snaps can detach, posing a choking hazard to children.

    Product
    Faux-Fur Hooded Bear Coats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V124000·2017-02-27

    Western Star 4900 Trucks Recalled for Air Tank Weld Defects

    Daimler Trucks North America is recalling 2015-2018 Western Star 4900 trucks because aluminum air tanks may have improper welds, risking rapid air pressure loss.

    Product
    WESTERN STAR — WESTERN STAR 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V126000·2017-02-27

    Thomas Built Buses Recalls Saf-T-Liner HDX for Steering Defect

    Daimler Trucks North America is recalling 2017-2018 Thomas Built Buses Saf-T-Liner HDX transit buses because a loose steering pinch bolt may cause loss of vehicle control.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V123000·2017-02-27

    Ford Recalls 2016-2017 Edge, MKX, Continental for Air Bag Defect

    Ford is recalling 2016-2017 Edge, MKX, and Continental vehicles because the driver's air bag may not fully inflate or detach during a crash.

    Product
    LINCOLN — LINCOLN, FORD MKX, CONTINENTAL, EDGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V122000·2017-02-27

    Horton Ambulances Recalled for Rear Brake Bolt Torque Issue

    Halcore Group is recalling 2017 Horton ambulances because overtightened rear brake bolts may cause loss of braking power, increasing crash risk.

    Product
    HORTON AMBULANCE — HORTON AMBULANCE CCO, 453, 623, 457
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V125000·2017-02-27

    Thomas Built Buses Recalls 2017-2018 Saf-T-Liner HDX School Buses

    Daimler Trucks North America is recalling 2017-2018 Thomas Built Buses Saf-T-Liner HDX school buses because a loose steering bolt may cause loss of vehicle control.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide