The Recall Desk

State

Northern Mariana Islands product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36476–36500 of 73760

  • ModerateFDA (Drugs)·D-0037-2019·2018-10-24

    Product Quest Recalls DG Health Nasal Pump Mist for CGMP Deviations

    Product Quest Manufacturing LLC is recalling 786,720 bottles of DG Health No Drip Nasal Pump Mist due to manufacturing deviations that could impact product quality.

    Product
    DG health, No Drip, Nasal Pump Mist (oxymetazoline hydrochloride), 0.05%, 1 FL OZ (30 mL) bottle, Distributed by: Dolgencorp, LLC, 100 Mission Ridge, Goodlettsville, TN 37072, UPC 7 27510 00373 3 .
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0048-2019·2018-10-24

    Premier Value Saline Nasal Spray Recalled for Quality Concerns

    Product Quest Manufacturing LLC is recalling Premier Value Saline Nasal Spray due to manufacturing deviations that could impact product quality.

    Product
    Premier Value, Saline Nasal Spray, Sodium Chloride 0.65%, packaged as a) 3 FL OZ (88 mL) bottle NDC 68016-388-00 UPC 8 40986 01483 3; b) 1.5 FL OZ (44 mL) bottle NDC 68016-466-00 UPC 8 40986 01482 6, Distributed By Chain Drug Consortium, 3301 NW Boca Raton Blvd, Suite 101, Boca…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0058-2019·2018-10-24

    FDA Recalls Best Choice Nasal Spray Due to Manufacturing Quality Issues

    Product Quest Manufacturing LLC is recalling 3,600 bottles of Best Choice Nasal Spray because they were manufactured under conditions that could impact product quality.

    Product
    Best Choice, 12 Hour No-Drip Nasal Spray (Oxymetazoline Hydrochloride 0.05%) Nasal Decongestant, 1 FL OZ (30 mL) bottle, Proudly Distributed By: Valu Merchandisers, Co., 5000 Kansas Ave, Kansas City, KS 66106, UPC 0 70038 59895 4.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0035-2019·2018-10-24

    CVS Health Saline Nasal Spray Recalled for Manufacturing Deviations

    Product Quest Manufacturing LLC is recalling 552 bottles of CVS Health Saline Nasal Spray due to CGMP deviations that could impact product quality.

    Product
    CVS Health, Saline Nasal Spray, 1.5 FL OZ bottle, Distributed by CVS Pharmacy, Inc. One CVS Drive Woonsocket, RI 02895, Product #277790.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0141-2019·2018-10-24

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Issues

    Zimmer Biomet is recalling 27 Affixus Hip Fracture Nails because sterile packaging was found open during surgery.

    Product
    Affixus Hip Fracture Nail Right 125 13 mm x 300 mm, Item Number 814313300 Product Usage: Intended for the fixation of fractures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0061-2019·2018-10-24

    Walgreens NO DRIP Anefrin Nasal Spray recall due to CGMP deviations

    This FDA drug recall affects Walgreens NO DRIP Anefrin nasal spray due to current good manufacturing practice deviations that could impact product quality.

    Product
    Walgreens, NO DRIP Anefrin Nasal Spray (Oxymetazoline HCl 0.05%), Nasal Decongestant, Extra Moisturizing, 12 Hour, 0.5 FL OZ (15 mL) bottle, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-7004-01, UPC 3 11917 18534 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0047-2019·2018-10-24

    FDA Recalls Premier Value Nasal Decongestant Spray Due to Quality Concerns

    Product Quest Manufacturing LLC is recalling Premier Value Nasal Decongestant Nasal Spray because it was manufactured under conditions that could impact product quality.

    Product
    Premier Value, Nasal Decongestant, Nasal Spray (oxymetazoline HCl 0.05%), Regular Strength, 1 FL OZ (30 mL) bottle, Distributed By Chain Drug Consortium, 3301 NW Boca Raton Blvd, Suite 101, Boca Raton, FL 33431, NDC 68016-316-03, UPC 8 40986 01516 8.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0144-2019·2018-10-24

    Zimmer Biomet Recalls Affixus Hip Fracture Nails Due to Packaging Issues

    Zimmer Biomet is recalling 25 Affixus Hip Fracture Nails because sterile packaging was found open during surgery. The recall covers units distributed in the US and abroad.

    Product
    Affixus Hip Fracture Nail Right 125 13 mm x 440 mm, Item Number 814313440 Product Usage: Intended for the fixation of fractures
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0069-2019·2018-10-24

    Well at Walgreens Scar Cream Recalled for Low Active Ingredient Levels

    Product Quest Manufacturing LLC is recalling 6,516 tubes of Well at Walgreens Scar Cream with SPF 30 because the octocrylene and avobenzone levels were found to be lower than required.

    Product
    Well at Walgreens, Scar Cream with SPF 30, (Avobenzone 3%, Octocrylene 10%, Oxybenzone 6%), 0.7 OZ (19.8 g) tube, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, UPC 3 11917 18281 0.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0249-2019·2018-10-24

    Amerigen Recalls Temozolomide Capsules Due to Dissolution Failures

    Amerigen Pharmaceuticals is recalling Temozolomide capsules because stability testing revealed out-of-specification dissolution results.

    Product
    Temozolomide capsules, 20 mg, packaged in a) 5-count bottle(NCD 43975-253-05), b) 14-count bottle (NDC 43975-253-14), Rx only, Mfd. by: Stason Pharmaceuticals, Inc., Irvine, CA 92618, Dist. By: Amerigen Pharmaceuticals, Lyndhurst, NJ 07071.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0070-2019·2018-10-24

    Cicatricure Scar Cream Recalled for Low Active Ingredient Levels

    Product Quest Manufacturing LLC is recalling Cicatricure Scar Cream + Sunscreen SPF 30 because the octocrylene and avobenzone levels were found to be lower than required.

    Product
    Cicatricure, Scar Cream + Sunscreen SPF 30 (avobenzone 3%, octocrylene 10%, oxybenzone 6%), 0.7 oz. (19.8 g) tube, Distributed by: Genomma Lab USA Inc., Houston, TX 77027, UPC 6 50067 00018 7.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V750000·2018-10-23

    Proterra Recalls 2016-2017 Catalyst Buses Due to Brake Caliper Defect

    Proterra is recalling 2016-2017 Catalyst transit buses because a defect in the brake calipers may cause the guide pin support bolt to break, potentially leading to loss of braking ability or tire pressure.

    Product
    PROTERRA — PROTERRA CATALYST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19018·2018-10-23

    Zeagle Sport Buoyancy Control Devices Recalled Due to Drowning Hazard

    Huish Outdoors is recalling Zeagle Sport buoyancy control devices because inflator buttons can break, causing rapid air loss or auto-inflation that poses a drowning risk to scuba divers.

    Product
    Zeagle Sport buoyancy control devices (BCDs)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V748000·2018-10-22

    E-One Recalls 2016-2018 Typhoon and Cyclone II Aerial Devices

    E-One is recalling 2016-2018 Typhoon and Cyclone II aerial devices because a torque rod tower may crack, potentially affecting vehicle handling and increasing crash risk.

    Product
    E-ONE — E-ONE CYCLONE II, TYPHOON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V747000·2018-10-22

    E-One Recalls 2012-2015 Emergency Vehicles Due to Fire Risk

    E-One is recalling 2012-2015 Typhoon, Cyclone II, and Cyclone III emergency vehicles because a melting relay in the HVAC system can increase the risk of a fire.

    Product
    E-ONE — E-ONE CYCLONE III, CYCLONE II, TYPHOON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V735000·2018-10-22

    Ford Recalls 2012-2018 Focus Models Due to Fuel System Defect

    Ford is recalling 2012-2018 Focus vehicles with 2.0L engines because a malfunctioning valve may cause the engine to stall while driving, increasing crash risk.

    Product
    FORD — FORD FOCUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V749000·2018-10-22

    E-One Recalls 2017 Classic Fire Vehicles Due to Pump Wiring Defect

    E-One is recalling 2017 Classic Fire emergency vehicles equipped with specific Kubota pumps that may be improperly wired, preventing warning lamps from illuminating.

    Product
    E-ONE — E-ONE CLASSIC FIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V746000·2018-10-22

    KME Commercial Skid Recall for Improperly Wired Pump Warning Lamps

    Kovatch Mobile Equipment is recalling 2015 and 2017 KME Commercial Skids because improperly wired pumps may fail to display oil pressure and temperature warnings.

    Product
    KME — KME COMMERCIAL SKID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V745000·2018-10-22

    Altec Recalls 2014-2018 Digger Derrick Vehicles for Software Defect

    Altec is recalling 2014-2018 Digger Derrick vehicles because the Zone Rating System may fail to alert operators to excessive loads, increasing injury risk.

    Product
    ALTEC — ALTEC DIGGER DERRICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·103-2018·2018-10-21

    Bakkavor Recalls Meat and Poultry Products Due to Possible Salmonella and Listeria

    Bakkavor Foods USA is recalling approximately 795,261 pounds of ready-to-eat meat and poultry products containing onions that may be contaminated with Salmonella and Listeria monocytogenes.

    Product
    Bakkavor Foods USA, Inc. Recalls Meat and Poultry Products due to Possible Salmonella and Listeria monocytogenes Contamination In Onions
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalUSDA FSIS·098-2018·2018-10-19

    Ruiz Food Products Recalls Taquitos Due to Salmonella and Listeria Concerns

    Ruiz Food Products is recalling approximately 2.5 million pounds of ready-to-eat beef and poultry taquitos due to possible Salmonella and Listeria contamination in onion ingredients.

    Product
    Ruiz Food Products, Inc. — Ruiz Food Products, Inc. Recalls Beef and Poultry Products due to Possible Salmonella and Listeria monocytogenes Contamination in Onion Ingredient
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V740000·2018-10-19

    Chrysler Recalls Pacifica Plug-in Hybrids for Engine Restart and Fire Risk

    Chrysler is recalling 2017-2018 Pacifica Plug-in Hybrids because the engine may fail to restart, causing unburned fuel to enter the exhaust and increasing crash or fire risks.

    Product
    CHRYSLER — CHRYSLER PACIFICA PLUG-IN HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V741000·2018-10-19

    Thor Motor Coach Recalls 2018-2019 Models Due to Propane Leak Risk

    Thor Motor Coach is recalling 2018-2019 Four Winds, Chateau, and Freedom Elite vehicles because a liquid propane hose may be damaged, creating a leak and fire risk.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH FREEDOM ELITE, CHATEAU, FOUR WINDS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·19017·2018-10-19

    Brookstone Wireless Speakers Recalled Due to Fire Hazard

    Brookstone is recalling Big Blue Party wireless speakers because their lithium-ion batteries can overheat and catch fire, posing a fire hazard.

    Product
    Wireless speakers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·100-2018·2018-10-19

    Envolve Foods Recalls Chicken and Beef Products Due to Contamination Concerns

    Envolve Foods is recalling approximately 292,764 pounds of ready-to-eat chicken and beef products due to possible Salmonella and Listeria monocytogenes contamination in vegetable ingredients.

    Product
    Envolve Foods Recalls Chicken and Beef Products due to Possible Salmonella and Listeria monocytogenes Contamination in Vegetables
    Category
    Food
    Distribution
    Distributed nationwide