The Recall Desk

State

Northern Mariana Islands product recalls

72,919 recalls have nationwide distribution and so reach Northern Mariana Islands. 22 additional recalls listed Northern Mariana Islands specifically in their distribution scope.

What the numbers show

Total
22
Critical
0
Severe
8
Most recent
2025-02-05

Of the 22 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 8 (36%) are Severe.

Which agencies issued them

These figures cover only the 22 recalls whose distribution notice names Northern Mariana Islands specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2851–2875 of 72941

  • ModerateFDA (Drugs)·D-0383-2026·2026-03-11

    Midodrine hydrochloride tablets recalled over inadequately sealed blister packaging

    The Harvard Drug Group is recalling one lot of Midodrine Hydrochloride Tablets 5 mg because of a defective container with inadequately sealed blister packaging.

    Product
    MIDODRINE HYDROCHLORIDE — MIDODRINE HYDROCHLORIDE (MIDODRINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0359-2026·2026-03-11

    First Aid Only BZK antiseptic towelettes recalled over manufacturing deviations

    Acme United Corporation is recalling First Aid Only BZK Antiseptic Towelettes over current good manufacturing practice deviations.

    Product
    FIRST AID ONLY BZK ANTISEPTIC — FIRST AID ONLY BZK ANTISEPTIC (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0366-2026·2026-03-11

    Med-Nap BZK antiseptic towelettes recalled over manufacturing practice deviations

    Acme United Corporation is recalling Med Nap BZK Antiseptic Towelettes in 100-count packs over current good manufacturing practice deviations.

    Product
    MED NAP BENZALKONIUM CHLORIDE ANTISEPTIC — MED NAP BENZALKONIUM CHLORIDE ANTISEPTIC (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0370-2026·2026-03-11

    Med-Nap cleansing towelette bulk packs recalled over manufacturing deviations

    Acme United Corporation is recalling Med-Nap Cleansing Towelettes in bulk cases over current good manufacturing practice deviations.

    Product
    MED NAP CLEANSING TOWELETTE — MED NAP CLEANSING TOWELETTE (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0365-2026·2026-03-11

    Medi-First antiseptic wipes recalled over manufacturing practice deviations

    Acme United Corporation is recalling Medi-First Antiseptic Wipes over current good manufacturing practice deviations.

    Product
    MEDI-FIRST ANTISEPTIC WIPES — MEDI-FIRST ANTISEPTIC WIPES (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0387-2026·2026-03-11

    Zone 2 lidocaine cream recalled because stability data does not support expiry

    HTO Nevada, trading as Kirkman, is recalling one lot of Maximum Zone 2 4% Lidocaine Cream because the stability data does not support the labeled expiry date.

    Product
    MAXIMUM, ZONE 2, 4% Lidocaine Cream, (Lidocaine 4% and Epinephrine 0.01%), 1 oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-015.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1492-2026·2026-03-11

    Vascular grafts recalled after expiry dates were calculated from packaging

    Vascutek is recalling Gelsoft Plus and Gelweave vascular prostheses because they were labeled with an additional month of shelf life, expiry having been calculated from packaging rather than gel impregnation.

    Product
    Gelsoft Plus, REF: 635024PE, 631514PE, 631222PE, 633008PE, 633010PE, 633007PE, 636010PE, 632522PE, 633012PE, 635018PE, 631516PE, 636016PE, 631220PE, 631608PE, 631206PE, 631407P50E, 631508PE, 636008PE, 636006PE, 632518PE, 634008PE, 634006PE, 631218PE, 632211PE, 634007PE, 633006PE,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1486-2026·2026-03-11

    Datascope CS100 balloon pump manual recalled for outdated battery specifications

    Datascope is recalling the CS100 IABP running software version Q.01 because the battery runtime and cycle specifications in the device's Instructions for Use need to be updated.

    Product
    CS100 IABP. Software Version CS100 IABP Q.01.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0385-2026·2026-03-11

    Vasocaine lidocaine spray recalled because stability data does not support expiry

    HTO Nevada, trading as Kirkman, is recalling Five-Star Vasocaine Spray because the stability data does not support the labeled expiry date.

    Product
    FIVE-STAR, VASOCAINE Spray, (Lidocaine HCl 4%, Racepinephrine HCl 0.01%), 4oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-016.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0373-2026·2026-03-11

    First Aid Only hand sanitizing wipes recalled over manufacturing deviations

    Acme United Corporation is recalling First Aid Only Hand Sanitizing Wipes over current good manufacturing practice deviations.

    Product
    FIRST AID ONLY HAND SANITIZING WIPE — FIRST AID ONLY HAND SANITIZING WIPE (ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0372-2026·2026-03-11

    WipesPlus hand sanitizing wipes recalled over manufacturing practice deviations

    Acme United Corporation is recalling WP WipesPlus Hand Sanitizing Wipes over current good manufacturing practice deviations.

    Product
    WP WipesPlus Hand Sanitizing Wipes (Benzalkonium Chloride 0.13%), 5x7, 100 CT, Progressive Products, 211 S. Ridge Street, Rye Brook, NY 10573. NDC 67151-727-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0363-2026·2026-03-11

    Max Packaging antibacterial towelettes recalled over manufacturing practice deviations

    Acme United Corporation is recalling Max Packaging Antibacterial Towelettes over current good manufacturing practice deviations.

    Product
    Max Packaging Antibacterial Towelette (Benzalkonium Chloride 0.13%), 1 towelette, 4x7, Max Packaging, Made in the USA, NDC 59647-750-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1487-2026·2026-03-11

    Datascope CS300 balloon pump manual recalled for outdated battery specifications

    Datascope is recalling the CS300 IABP running software version C.01 because the battery runtime and cycle specifications in the device's Instructions for Use need to be updated.

    Product
    CS300 IABP. Software Version CS300 IABP C.01.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0380-2026·2026-03-11

    Semaglutide compounding ingredient recalled over incomplete process and endotoxin validation

    Harbin Jixianglong Biotech is recalling Semaglutide for prescription compounding use because process validation and bacterial endotoxin method validation were not completed before distribution.

    Product
    Semaglutide, For Rx compounding use only, packaged in a) 1g, NDC 84385-106-01; b) 5g, NDC 84385-106-02; c) 10g, NDC 84385-106-06; d) 25g, NDC 84385-106-03; d) 50g, NDC 84385-106-04; e) 100g, NDC 84385-106-05Manufacturer: Harbin Jixianglong Biotech Co., Ltd., North of Baoan Road,
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0378-2026·2026-03-11

    Antimicrobial alcohol hand wipes recalled over manufacturing practice deviations

    Acme United Corporation is recalling Antimicrobial Alcohol Hand Wipes containing 70% isopropyl alcohol over current good manufacturing practice deviations.

    Product
    Antimicrobial Alcohol Hand Wipe, Isopropyl Alcohol 70%, Manufactured for : Custom Packaging Co., Inc, Louisville, KY 4023, NDC 0924-251-00.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0382-2026·2026-03-11

    Nilotinib 200 mg capsules recalled after failing appearance tests

    Cipla USA is recalling one lot of Nilotinib Capsules 200 mg after out-of-specification results in description and visual appearance testing at six-month long-term stability.

    Product
    NILOTINIB — NILOTINIB (NILOTINIB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0381-2026·2026-03-11

    Nilotinib capsules recalled after failing appearance tests at six months

    Cipla USA is recalling three lots of Nilotinib Capsules 150 mg after out-of-specification results in description and visual appearance testing at six-month long-term stability.

    Product
    NILOTINIB — NILOTINIB (NILOTINIB)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·26V135000·2026-03-06

    2026 Kia K4 vehicles recalled for defective rear seat belt anchor

    Kia is recalling certain 2026 K4 vehicles because the rear center seat belt anchor buckle may not latch properly, risking occupant restraint failure in a crash.

    Product
    KIA — KIA TELLURIDE, K4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V134000·2026-03-06

    Mercedes-Benz Recalls 2026 GLA 250 for Door Latch Defect

    Mercedes-Benz is recalling 2026 GLA 250 vehicles because an incorrectly installed bowden cable may prevent the door from opening from inside, potentially trapping occupants.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLA 250
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V129000·2026-03-05

    GM heavy duty pickup fuel pump may cause an engine stall

    GM is recalling certain 2025-2026 Chevrolet Silverado 3500 and GMC Sierra 3500 vehicles with gasoline engines and dual fuel tanks because the rear fuel pump may not transfer adequate fuel to the front tank.

    Product
    GMC — GMC, CHEVROLET SIERRA 3500, SILVERADO 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V128000·2026-03-05

    Toyota Highlander second-row seat backs may fail to lock

    Toyota is recalling certain 2021-2024 Highlander and Highlander Hybrid vehicles because the second-row seat backs may fail to lock into position during seat back adjustment.

    Product
    TOYOTA — TOYOTA HIGHLANDER, HIGHLANDER HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide