The Recall Desk

State

Northern Mariana Islands product recalls

73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

30876–30900 of 73745

  • SevereCPSC·20036·2019-12-06

    Surly Recalls Front Bicycle Racks Due to Crash and Injury Hazards

    Surly Bikes is recalling about 5,139 front bicycle racks because they can loosen and contact the front wheel, posing crash and injury hazards.

    Product
    Surly front bicycle racks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V866000·2019-12-06

    Volkswagen Recalls 2013-2015 Jetta Hybrid for Transmission Defect

    Volkswagen is recalling 2013-2015 Jetta Hybrid vehicles because hairline cracks in the transmission can cause oil leaks and sudden loss of drive power, increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20035·2019-12-06

    Trek Recalls Super Commuter+ Electric Bicycles Due to Fall Hazard

    Trek is recalling about 2,840 Super Commuter+ 8S electric bicycles because a front fender bolt can unthread, causing the wheel to detach and posing a fall hazard.

    Product
    Trek Super Commuter+ 8S
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V869000·2019-12-06

    Daimler Recalls 2020-2021 Thomas Built Saf-T-Liner C2 School Buses

    Daimler Trucks North America is recalling 145 school buses due to loose fan hub bolts that could damage components or detach, risking injury during an uncontrolled stop.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V867000·2019-12-06

    Mercedes-Benz Recalls 2020 GLE 450 for Third-Row Headrest Defect

    Mercedes-Benz is recalling one 2020 GLE 450 4MATIC because third-row headrests may not hold in place, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLE 450
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V868000·2019-12-06

    Mercedes-Benz Recalls 2019 AMG E-Class Models for Air Bag Defect

    Mercedes-Benz is recalling 2019 AMG E53, E63, and E63S models because incorrect driver air bags and software may be installed, increasing injury risk in crashes.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG E63S, E63, AMG E53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V865000·2019-12-05

    Honda Recalls 2019-2020 CR-V for Rear Subframe Bolt Defect

    Honda is recalling 2019-2020 CR-V vehicles because improperly manufactured rear subframe bolts may loosen, allowing the subframe to separate and increasing crash risk.

    Product
    HONDA — HONDA CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·20711·2019-12-05

    DaVinci Bailey Bassinets Recalled Due to Support Leg Breakage Hazard

    DaVinci is recalling about 3,000 Bailey bassinets because support legs can break, posing a fall hazard to infants. Consumers should stop using them and contact the company for a repair kit.

    Product
    DaVinci Bailey bassinets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0528-2020·2019-12-04

    Aurobindo Ranitidine Capsules Recalled for NDMA Contamination

    AuroMedics Pharma LLC is recalling Aurobindo Ranitidine Capsules 300 mg because N-nitrosodimethylamine (NDMA) was detected in the product.

    Product
    Aurobindo Ranitidine Capsules 300 mg, 30-count bottle, Rx Only Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 NDC 59651-145-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0523-2020·2019-12-04

    New Vitalis Pharmacy Recalls Testosterone Injection Due to Sterility Concerns

    New Vitalis Pharmacy is recalling Testosterone Cypionate and Propionate oil injection solutions due to a lack of sterility assurance.

    Product
    Testosterone Cypionate 180 mg/mL/Testosterone Propionate 20mg/mL Oil Injection Solution, 10 mL per vial, New Vitalis Pharmacy
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0525-2020·2019-12-04

    AVKARE Recalls Ranitidine Tablets Due to NDMA Impurity

    AVKARE Inc. is recalling specific lots of Ranitidine Tablets 300 mg because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).

    Product
    AVKARE Ranitidine Tablets, USP 300 mg Rx Only NDC Manufactured for: AvKARE, Inc. Pulaski, TN 38478 a) 250 tablets NDC 42291-725-25; b) 30 tablets NDC 42291-725-30
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0524-2020·2019-12-04

    AVKARE Recalls Ranitidine Tablets Due to NDMA Impurity

    AVKARE Inc. is recalling specific lots of Ranitidine Tablets 150 mg because the active ingredient contained the impurity N-nitrosodimethylamine (NDMA).

    Product
    AVKARE Ranitidine Tablets, USP 150 mg Rx Only Manufactured for: AvKARE, Inc. Pulaski, TN 38478 Manufactured by: Amneal Pharmaceuticals of NY Hauppauge, NY 11788 a) 1000 tablets NDC 42291-724-10; b) 180 tablets NDC 42291-724-18; c) 60 tablets NDC 42291-724-60
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0526-2020·2019-12-04

    AuroMedics Recalls Ranitidine Tablets Due to NDMA Detection

    AuroMedics Pharma LLC is recalling DG Health Acid Reducer Ranitidine Tablets 150 mg because N-nitrosodimethylamine (NDMA) was detected in the product.

    Product
    DG Health Acid Reducer Ranitidine Tablets 150 mg, 8-count carton, Distributed by: Dolgencorp LLC 100 Mission Ridge Goodletville TN 37072 NDC 55910-092-79
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0529-2020·2019-12-04

    AuroMedics Recalls Ranitidine Syrup Due to NDMA Contamination

    AuroMedics Pharma LLC is recalling Ranitidine Syrup because N-nitrosodimethylamine (NDMA) has been detected in the product.

    Product
    Ranitidine Syrup (Ranitidine Oral Solution, USP), 15 mg/mL (75 mg/5mL) 474 mL bottle, Rx only Distributed by: Aurobindo Pharma USA Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 Made in India NDC 65862-431-74
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0573-2020·2019-12-04

    AuroMedics Recalls MARLIDO KIT Vials Due to Foreign Material Presence

    AuroMedics Pharma LLC is recalling MARLIDO KIT vials because foreign material was found inside the vials. The affected product is Lidocaine HCl Injection, USP, 2%.

    Product
    MARLIDO KIT — MARLIDO KIT (MARCAINE, LIDOCAINE, POVIDONE IODINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V860000·2019-12-04

    REV Recalls Fleetwood and Holiday Rambler Motorhomes Due to Exhaust Defect

    REV Recreation Group is recalling 3,241 Fleetwood and Holiday Rambler motorhomes because the generator exhaust pipe placement may allow carbon monoxide to enter the vehicle.

    Product
    FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER BOUNDER, VACATIONER, SOUTHWIND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0521-2020·2019-12-04

    Zimmer Biomet Recalls Acromium Flange Sets Due to Cleaning Issues

    Zimmer Biomet is recalling Acromium Flange Sets because elevated levels of bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.

    Product
    ACROMIUM FLANGE SET (Custom product) Item No. PM555148 - Product Usage: Arcomium replacement.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0530-2020·2019-12-04

    Aurobindo Ranitidine Capsules Recalled for NDMA Contamination

    AuroMedics Pharma LLC is recalling Aurobindo Ranitidine Capsules 150 mg because N-nitrosodimethylamine (NDMA) was detected in the product.

    Product
    Aurobindo Ranitidine Capsules 150 mg, 500 count bottle, Rx Only Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 NDC 59651-144-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V859000·2019-12-04

    Ford Recalls 2020 Explorer and Lincoln Aviator for Fuel Leak Risk

    Ford is recalling 2020 Explorer and Lincoln Aviator vehicles because a chafing fuel line may cause a leak, increasing the risk of fire.

    Product
    FORD — FORD, LINCOLN EXPLORER, AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0527-2020·2019-12-04

    Aurobindo Ranitidine Capsules Recalled for NDMA Contamination

    AuroMedics Pharma LLC is recalling Aurobindo Ranitidine Capsules 150 mg because N-nitrosodimethylamine (NDMA) was detected in the product.

    Product
    Aurobindo Ranitidine Caspules 150 mg, 60-count bottle, Rx Only Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 08520 NDC 59651-144-60
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V862000·2019-12-04

    Volkswagen Recalls Diesel Vehicles for Air Bag Inflator Defect

    Volkswagen is recalling certain 2011-2015 Golf, Passat, and Audi A3 diesel vehicles because the driver's side air bag inflator may explode.

    Product
    VOLKSWAGEN — VOLKSWAGEN, AUDI GOLF, A3, PASSAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0519-2020·2019-12-04

    Zimmer Biomet Recalls Compress Mini Compress Devices Due to Cleaning Issues

    Zimmer Biomet is recalling Compress Mini Compress devices because elevated bacterial endotoxin and residual debris remain on the devices due to a cleaning issue.

    Product
    Compress, Mini Compress; Item Nos. 178350 178351 178352 178353 178354 178355 178356 178357 178358 178359 178360 178361 178362 178363 178364 178365 178366 178367 178368 178369 178370 178371 178372 178373 178464 178472 178480 178488 178496 178504…
    Category
    Medical Device
    Distribution
    Distributed nationwide