The Recall Desk

State

Northern Mariana Islands product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

36976–37000 of 73761

  • ModerateFDA (Devices)·Z-2994-2018·2018-09-19

    Diagnostica Stago Recalls STA N¿oplastine¿ CI Reagents Due to Quality Control Issues

    Diagnostica Stago is recalling STA N¿oplastine¿ CI in-vitro diagnostic kits because quality control values fell outside assigned ranges, potentially affecting prothrombin time test results.

    Product
    Diagnostica Stago STA N¿oplastine¿ CI, 10 ml vial. In-Vitro Diagnostic for determination of the prothrombin time (PT) in plasma. REF: 00666 The STA¿ - N¿oplastine¿ CI kits provide reagents for the determination of the prothrombin time (PT) in plasma with STA-R¿, STA…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2993-2018·2018-09-19

    Diagnostica Stago Recalls STA N¿oplastine¿ CI Plus Reagents Due to Quality Control Failures

    Diagnostica Stago is recalling 24,043 kits of STA N¿oplastine¿ CI Plus reagents because quality control values fell outside assigned ranges, potentially affecting prothrombin time test results.

    Product
    Diagnostica Stago STA N¿oplastine¿ CI Plus, 10 ml vial. In-Vitro Diagnostic for determination of the prothrombin time (PT) in plasma. (REF 00667) The STA¿ - N¿oplastine¿ CI Plus kits provide reagents for the determination of the prothrombin time (PT) in plasma with STA-R¿…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1184-2018·2018-09-19

    Pfizer Recalls Argatroban Injection Vials Due to Stability Testing Failures

    Pfizer is recalling 1,580 vials of Argatroban Injection because stability testing results were out of specification at the 18-month time point.

    Product
    Argatroban Injection, 250 mg/2.5 mL (100 mg/mL), 2.5 mL Single-use Vial, Rx only, Sterile, Manufactured for: Hospira, Inc, Lake Forest, IL 60045 USA. NDC: 0409-1140-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1185-2018·2018-09-19

    Par Pharmaceutical Recalls Pramipexole Dihydrochloride Extended Release Tablets

    Par Pharmaceutical is recalling Pramipexole dihydrochloride extended release tablets because they contain a known impurity at levels exceeding specifications.

    Product
    Pramipexole dihydrochloride extended release tablets, 0.75 mg, packaged in 30-count bottles, Rx only, Manufactured by: Par Pharmaceutical, Chestnut Ridge, NY 10977, NDC 10370-252-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-3043-2018·2018-09-19

    Ortho-Clinical Diagnostics Recalls VITROS Chemistry Products Cl- Slides

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Cl- Slides because they do not meet maximum allowable interference claims for triglycerides in serum samples.

    Product
    VITROS Chemistry Products Cl- Slides, Product Code 844 5207 Product Usage: For in vitro diagnostic use only. VITROS Chemistry Products Cl- Slides quantitatively measure chloride (Cl-) concentration in serum and plasma using VITROS 250/350/5,1 FS and 4600 Chemistry Systems…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-3044-2018·2018-09-19

    Ortho-Clinical VITROS Chloride Slides Recalled for Interference Issues

    Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products Cl- Slides because they do not meet maximum allowable interference claims for triglycerides.

    Product
    VITROS Chemistry Products Cl- Slides, Product Code 684 4471 Product Usage For in vitro diagnostic use only. VITROS Chemistry Products Cl- Slides quantitatively measure chloride (Cl-) concentration in serum, plasma and urine using VITROS 250/350/5,1 FS and 4600 Chemistry…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1187-2018·2018-09-19

    Mylan Recalls Diltiazem HCl Extended-Release Capsules Due to Impurities

    Mylan Pharmaceuticals is recalling 656 bottles of Diltiazem HCl Extended-Release Capsules 120 mg because routine stability testing found out-of-specification related compounds.

    Product
    Diltiazem HCl Extended-Release Capsules, USP 120 mg 500-count bottle, Rx only, Mylan Pharmaceuticals Inc. Morgantown, WV 26505. NDC 0378-5220-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1186-2018·2018-09-19

    Mylan Recalls Diltiazem HCl Extended-Release Capsules Due to Impurities

    Mylan Pharmaceuticals is recalling Diltiazem HCl Extended-Release Capsules 120 mg because routine stability testing revealed out-of-specification results for related compounds.

    Product
    Diltiazem HCl Extended-Release Capsules, USP 120 mg 100-count bottle, Rx only, Mylan Pharmaceuticals Inc. Morgantown, WV 26505. NDC 0378-5220-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·18V640000·2018-09-18

    Forest River Recalls Buses with Defective Wheelchair Lifts

    Forest River is recalling specific 2012-2018 buses because a wheelchair lift component may fail, allowing the platform to rise too high and increasing injury risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS, ELKHART, GLAVAL BUS ALLSTAR XL MVP, ALLSTAR, SENATOR II, STARLITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V639000·2018-09-17

    Audi Recalls 2017-2018 R8 Vehicles Due to Transmission Fluid Leak Fire Risk

    Volkswagen Group of America is recalling 2017-2018 Audi R8 Spyder and Coupe vehicles because transmission fluid may leak from the gearbox ventilation hose, creating a fire risk if it contacts hot engine parts.

    Product
    AUDI — AUDI R8 SPYDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V642000·2018-09-17

    Heil Recalls 2014-2016 Garbage Trucks Due to Cracking Hydraulic Brackets

    Heil Environmental is recalling 2014-2016 garbage trucks because hydraulic oil tank brackets may crack, causing oil leaks that increase crash risk.

    Product
    HEIL — HEIL FRONT END LOADER GARBAGE, SIDE LOADER GARBAGE TRUCK, ROLLOFF BODY/HOIST, REAR LOADER GARBAGE TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V638000·2018-09-14

    Trail King Recalls 2016-2018 Trailers Due to Cracking Cross Members

    Trail King is recalling 2016-2018 ACS and AACS trailers because aluminum cross members may crack, potentially causing the suspension to loosen and increasing crash risk.

    Product
    TRAIL KING — TRAIL KING ACS, AACS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V636000·2018-09-14

    Alfa Romeo Giulia and Stelvio Recalled for Engine Fire Risk

    Chrysler is recalling 2017-2018 Alfa Romeo Giulia and 2018 Stelvio vehicles because engine misfires may overheat the catalytic converter, potentially causing a fire or engine stall.

    Product
    ALFA ROMEO — ALFA ROMEO GIULIA, STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V621000·2018-09-14

    Mitsubishi Recalls Outlander Models Due to Safety System Software Defect

    Mitsubishi is recalling 2017-2018 Outlander, Outlander Sport, Eclipse Cross, and Outlander PHEV vehicles because incorrect software may prevent safety systems like automatic emergency braking from functioning.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER, OUTLANDER SPORT, ECLIPSE CROSS, OUTLANDER PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V635000·2018-09-14

    Alfa Romeo Stelvio Recall: Engine Cooling Hose Defect

    Chrysler is recalling 2018-2019 Alfa Romeo Stelvio Quadrifoglio vehicles because an engine cooling hose may leak coolant, causing overheating and stalling.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V633000·2018-09-14

    Cruiser RV Recalls 2019 Travel Trailers Due to Axle Bearing Defect

    Cruiser RV is recalling 2019 travel trailers because missing inner bearing races may cause hub failure and increase crash risk.

    Product
    CRUISER RV — CRUISER RV RADIANCE ULTRA LITE, MPG, FUN FINDER EXTREME LITE, SHADOW CRUISER ULTRA LITE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V632000·2018-09-14

    Bentley Recalls 2018 Mulsanne and Bentayga for Rearview Camera Issues

    Bentley is recalling 2018 Mulsanne and Bentayga vehicles because the rearview camera display may be obstructed or delayed, increasing crash risk when reversing.

    Product
    BENTLEY — BENTLEY BENTAYGA, MULSANNE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V620000·2018-09-14

    Mitsubishi Recalls Outlander and Eclipse Cross Models for Braking Software Defect

    Mitsubishi is recalling certain 2017-2019 Outlander, Outlander Sport, Eclipse Cross, and Outlander PHEV vehicles because faulty software may cause the Forward Collision Mitigation system to brake for too long, increasing the risk of a rear-end collision.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER, OUTLANDER SPORT, ECLIPSE CROSS, OUTLANDER PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V630000·2018-09-13

    Honda Recalls 2018 CRF250L Motorcycles Due to Wiring Harness Defect

    Honda is recalling 2018 CRF250L motorcycles because an improperly installed wiring harness may damage safety components like lights and the horn, increasing crash risk.

    Product
    HONDA — HONDA CRF250L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V628000·2018-09-13

    Forest River Recalls 2019 East to West Travel Trailers Due to Axle Issue

    Forest River is recalling 2019 East to West travel trailers because incorrect axle shackles may allow tires to contact the wheel well, risking tire failure and loss of control.

    Product
    FOREST RIVER — FOREST RIVER EAST TO WEST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V624000·2018-09-13

    Forest River Recalls 2019 Travel Trailers Due to Axle Bearing Defect

    Forest River is recalling 2019 travel trailers because missing inner bearing races may cause hub overheating or separation, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN XLR, VIBE, SIERRA, SHASTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V626000·2018-09-13

    Subaru Recalls 2010-2014 Legacy and Outback for Parking Brake Defect

    Subaru is recalling 2010-2014 Legacy and Outback vehicles with manual transmissions because the electronic parking brake may fail to engage, increasing the risk of a crash.

    Product
    SUBARU — SUBARU LEGACY, OUTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide