The Recall Desk

State

Northern Mariana Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

57526–57550 of 73856

  • ModerateFDA (Drugs)·D-1488-2014·2014-08-06

    Dermamedics Calm & Correct Cream Recalled for Lack of FDA Approval

    Dermamedics, L.L.C. is recalling Calm & Correct Cream because the FDA determined the product is an unapproved new drug and misbranded.

    Product
    Dermamedics Calm & Correct Cream in 2 oz. containers with SKU number DM1020.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2228-2014·2014-08-06

    Purefruit Chile Recalls Market Pantry Applesauce Pouches Due to Mold Risk

    Purefruit Chile S.A. is recalling Market Pantry applesauce pouches due to the possibility of mold. The product was distributed nationwide.

    Product
    Market Pantry Apple; 3.5 oz/12 pk applesauce is packed into a labeled aluminum pouch with plastic screw-on lid and then placed into a labeled cardboard box; product is labeled in part, "***market pantry Apple Fruit Pouch***NET WT 3.5 OZ (100g)***DISTRIBUTED BY TARGET CORPORATION…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1504-2014·2014-08-06

    Daiichi Sankyo Recalls Tribenzor Tablets Due to Temperature Abuse

    Daiichi Sankyo is recalling specific lots of Tribenzor tablets because they were not stored at controlled room temperature during shipping.

    Product
    Tribenzor Tablets (olmesartan medoxomil/amlodipine/hydrochlorothiazide), 40 mg/5 mg*/25 mg 30 count bottles, Rx Only Manufactured for: Daiichi Sankyo, Inc., Parsippany, NJ 07054 --- NDC 65597-116-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2232-2014·2014-08-06

    Purefruit Chile Recalls HyVee Applesauce Pouches Due to Mold Risk

    Purefruit Chile S.A. is recalling specific HyVee applesauce pouches due to the possibility of mold. Consumers should check their pantry for the affected product.

    Product
    HyVee applesauce; 3.5 oz applesauce in aluminum pouch with plastic screw-on lid; product is labeled in part, "***HyVee Mother's Choice Apple organic baby food NET WT 3.5 OZ (99g)***INGREDIENTS:ORGANIC APPLE, ASCORBIC ACID DISTRIBUTED BY HY-VEE, INC WEST DES MOINES, IA 50266…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1501-2014·2014-08-06

    Daiichi Sankyo Recalls Azor Tablets Due to Temperature Abuse During Shipping

    Daiichi Sankyo is recalling 5 bottles of Azor Tablets (amlodipine and olmesartan medoxomil) 10 mg/40 mg because they were not stored at controlled room temperature during shipping.

    Product
    Azor Tablets (amlodipine and olmesartan medoxomil) 10 mg*/40 mg, 30 count bottles, Rx Only, Manufactured for: Daiichi Sankyo, Inc. Parsippany, NJ 07054 NDC 65597-113-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2132-2014·2014-08-06

    Nidek MC-500 Laser Photocoagulator Recalled for Missing Aperture Label

    Nidek Inc. is recalling 29 MC-500 Multicolor Laser Photocoagulators because the laser aperture label was not affixed to the devices prior to shipment.

    Product
    MC-500 Multicolor Laser Photocoagulator; Distributed by NIDEK Inc. Manufactured by NIDEK CO., Ltd, Japan. For use in ophthalmic and retinal procedures.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1507-2014·2014-08-06

    Benicar HCT Tablets Recalled Due to Temperature Abuse During Shipping

    Daiichi Sankyo is recalling 86 bottles of Benicar HCT 40 mg/12.5 mg because they were not stored at controlled room temperature during shipping.

    Product
    Benicar HCT Tablets (olmesartan medoxomil/hydrochlorothiazide) 40 mg/12.5 mg, 30 count bottles, Rx Only, Manufactured for: Daiichi Sankyo, Inc., Parsippany, NJ 07054 --- NDC 65597-106-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2134-2014·2014-08-06

    Brainlab Patient Data Manager 2.0 Software Recall for Image Display Defects

    Brainlab AG is recalling Patient Data Manager 2.0 software due to defects in transferring and displaying non-square pixel medical images.

    Product
    Patient Data Manager 2.0 (Content manager 2.0, Patient Browser 4.0, DICOM Viewer 2.0) Brainlab Digital Lightbox. A system for the display of medical images. Model numbers 25100-05 and 25100-06. The software can transfer images to and from picture archiving and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2230-2014·2014-08-06

    Purefruit Chile Recalls Pouched Applesauce Due to Potential Mold

    Purefruit Chile S.A. is recalling fruty U applesauce pouches due to the possibility of mold. The product was distributed to retail stores nationwide.

    Product
    fruty U applesauce, apple; 3.5 oz/20 pk applesauce is packed into a labeled aluminum pouch with plastic screw-on lid and then placed into a labeled cardboard box; product is labeled in part, "***fruty U APPLE applesauce***NET WEIGHT 3.53 OZ***FRUTY U www.frutyu.com Product of…
    Category
    Food
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1486-2014·2014-08-06

    Oxycodone Hydrochloride Oral Solution Recalled for Stability Failure

    Boehringer Ingelheim Roxane Inc is recalling 2,149 vials of Oxycodone Hydrochloride Oral Solution due to out-of-specification preservative levels.

    Product
    OXYCODONE HYDROCHLORIDE C II Oral Solution USP, 5 mg/5 mL, 15 mL Vial, Rx only. Boehringer Ingelheim, Roxane Laboratories. Roxane Laboratories, Inc. Columbus, Ohio 43216. NDC: 0054-0523-41.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1485-2014·2014-08-06

    Pfizer Recalls Cardura XL Tablets Due to Degradation Specifications

    Pfizer is recalling 22,461 bottles of Cardura XL 4 mg tablets because the product may not meet specifications for a product degradant.

    Product
    Cardura XL (doxazosin mesylate extended release tablets, 4 mg, 30-count bottle, Rx only, Distributed by Roerig Division of Pfizer Inc., New York, NY 10017, NDC 0049-2710-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2127-2014·2014-08-06

    Small Bone Innovations Recalls AutoFIX Cannulated Compression Screw Systems for IFU Update

    Small Bone Innovations is recalling 506 units of 3.0/4.0mm AutoFIX Cannulated Compression Screw Systems to update the Instructions for Use (IFU).

    Product
    Small Bone Innovations 3.0/4.0mm AutoFIX" Cannulated Compression Screw System Sets, Implants, and Instruments Indications for Use: AutoFIX" cannu lated screws are indicated for the treatment of fractures, non-unions, pseudoarthrosis and degenerative changes as well as…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·14250·2014-08-05

    Samson International Recalls Spencer Bar Stool Due to Fall Hazard

    Samson International is recalling Spencer Bar Stools sold at Costco because the footrest can crack, posing a fall hazard. No injuries have been reported.

    Product
    Spencer Bar Stool
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14249·2014-08-05

    Scubapro Aladin2 Dive Computers Recalled for Decompression Sickness Risk

    Johnson Outdoors Diving is recalling Scubapro Aladin2 dive computers because they may leak and stop working, posing a risk of injury from decompression sickness.

    Product
    Scubapro Aladin2 dive computers, commonly referred to as Aladin Square dive computers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V476000·2014-08-04

    Grand Design Recalls 2014 Momentum Trailers Due to Suspension Bolt Defect

    Grand Design is recalling 2014 Momentum 355th, 380th, and 385th fifth wheel trailers because suspension bolts may shear, potentially causing a crash.

    Product
    GRAND DESIGN — GRAND DESIGN MOMENTUM 355TH, MOMENTUM 380TH, MOMENTUM 385TH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V475000·2014-08-04

    Toyota Recalls FJ Cruiser and Tacoma for Incorrect Tire Placard Information

    Toyota is recalling 2008-2014 FJ Cruiser and Tacoma vehicles with specific accessory wheels because the tire placard may list incorrect spare tire size or inflation pressure.

    Product
    TOYOTA — TOYOTA FJ CRUISER, TACOMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V473000·2014-08-01

    Nova Bus Recalls 2013 LFS Transit Buses for Wiper Linkage Bolt Issue

    Nova Bus is recalling 189 model year 2013 LFS transit buses because a windshield wiper linkage bolt may loosen, potentially rendering wipers inoperable and increasing crash risk.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V467000·2014-07-31

    Jayco Recalls 2013-2014 Seneca Motorhomes Due to Fire Risk

    Jayco is recalling 2013-2014 Seneca motorhomes because water infiltration into the entrance door keypad may cause corrosion and an electrical short, increasing the risk of a fire.

    Product
    JAYCO — JAYCO SENECA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V469000·2014-07-31

    Schwarze M6000SE CNG Street Sweepers Recalled for Fire Risk

    Schwarze is recalling 2009 M6000SE CNG street sweepers because condensation in the intake manifold may freeze, causing sensor failure and potential exhaust fires.

    Product
    SCHWARZE — SCHWARZE M6000SE CNG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14245·2014-07-31

    Dynacraft Recalls Avigo Youth Bicycles Due to Front Wheel Detachment Hazard

    Dynacraft is recalling Avigo 20-inch youth bicycles because the front wheel can detach, posing a fall hazard. One injury involving scrapes and abrasions has been reported.

    Product
    Avigo 20-inch Turn N' Burn Youth Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide