The Recall Desk

State

Northern Mariana Islands product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

49551–49575 of 73840

  • ModerateFDA (Devices)·Z-1066-2016·2016-03-16

    Philips Allura Xper X-Ray Systems Recalled for Fluoroscopy Failure

    Philips is recalling 196 Allura Xper X-ray systems because they may display a 'Fluoro failed' error message when initiating fluoroscopy.

    Product
    Philips X-Ray Systems, Allura Xper with R8.2.16 Product Usage: The Allura Xper FD1O and Allura Xper FD1O/10 is intended for use in cardiovascular and vascular X-ray imaging applications, including diagnostic, interventional procedures (such as PTCA, stent placement and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1083-2016·2016-03-16

    Ormco Recalls TF Adaptive Gutta Percha Points Due to Labeling Error

    Ormco is recalling TF Adaptive Gutta Percha Points because the inner label is misidentified as ML3, though the outer package correctly identifies the product as SM3.

    Product
    TF Adaptive Gutta Percha Point Size SM3 50pk, Part No. 815-1541 Intended to fill a endontontically obturated root canal treatment
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1071-2016·2016-03-16

    Ortho-Clinical VITROS 250 Chemistry Systems Recalled for Condition Code Errors

    Ortho-Clinical Diagnostics is recalling VITROS 250 Chemistry Systems due to increased U90-382 or 6LU condition codes generated when using Calibrator Kit 9, Lot 954.

    Product
    VITROS 250 Chemistry Systems, Catalog 8132086, Unique Device Identifier No. 10758750004409, and VITROS 250 Refurbished, Catalog 6801759, Unique Device Identifier No. 10758750001330; IVD. Product Usage: For in vitro diagnostic use. The VITROS 250 Chemistry System performs…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1075-2016·2016-03-16

    Ortho-Clinical VITROS 5,1 FS Chemistry System Recall for Software Defect

    Ortho-Clinical Diagnostics is recalling VITROS 5,1 FS Chemistry Systems due to increased error codes generated when using a specific calibrator lot.

    Product
    VITROS 5,1 FS Chemistry System, Catalog Number 6801375, Unique Device Identifier Number 10758750001132; and VITROS 5,1 FS Chemistry System (Refurbished), Catalog Number 6801890, Unique Device Identifier Number 10758750001644; IVD. Product Usage: The VITROS 5,1 FS Chemistry…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0770-2016·2016-03-16

    FDA Recalls Atorvastatin Calcium 80 mg Due to Impurity Failures

    Golden State Medical Supply Inc. is recalling specific lots of Atorvastatin Calcium 80 mg tablets because they failed impurity and degradation specifications.

    Product
    Atorvastatin Calcium 80 mg, 10 tablets per blister,100-count package, Rx Only Manufactured by Apotex Inc. Toronto, Ontario, Canada, Packaged by GSMS Inc., Camarillo, CA 93010, NDC # 60429-326-77
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0769-2016·2016-03-16

    Atorvastatin Calcium 40 mg Recalled for Impurity Failures

    Golden State Medical Supply Inc. is recalling Atorvastatin Calcium 40 mg tablets due to failed impurities and degradation specifications.

    Product
    Atorvastatin Calcium 40 mg, 10 tablets per blister,100-count package, Rx Only Manufactured by Apotex Inc. Toronto, Ontario, Canada, Packaged by GSMS Inc., Camarillo, CA 93010, NDC # 60429-325-77
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0768-2016·2016-03-16

    Golden State Medical Supply Recalls Atorvastatin Calcium 20 mg Tablets

    Golden State Medical Supply is recalling specific lots of Atorvastatin Calcium 20 mg tablets due to failed impurities and degradation specifications.

    Product
    Atorvastatin Calcium 20 mg, 10 tablets per blister,100-count package, Rx Only Manufactured by Apotex Inc. Toronto, Ontario, Canada, Packaged by GSMS Inc., Camarillo, CA 93010, NDC # 60429-324-77
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·16119·2016-03-15

    Franklin Fueling Systems Recalls Gas Station Hose Swivel Fitting Sets

    Franklin Fueling Systems is recalling gas station hose and swivel fitting sets because the fitting can separate, causing fuel leaks and fire hazards.

    Product
    Gas station hose/swivel fitting sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16T003000·2016-03-15

    Cooper Roadmaster RM234 Tires Recalled for Sidewall Defect

    Cooper Tire & Rubber Co. is recalling specific Roadmaster RM234 tires due to a potential sidewall hole that could cause sudden tire failure.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V149000·2016-03-11

    Nissan Recalls 2014 Rogue Vehicles for Fuel Pump Failure Risk

    Nissan is recalling 46,671 model year 2014 Rogue vehicles because a fuel pump defect may cause the vehicle to stall without warning, increasing the risk of a crash.

    Product
    NISSAN — NISSAN ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V151000·2016-03-11

    GM Recalls 2016 Chevrolet Malibus for Side Air Bag Weld Defect

    General Motors is recalling 2016 Chevrolet Malibus because side air bag weld studs may fracture, increasing injury risk during deployment.

    Product
    CHEVROLET — CHEVROLET MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V152000·2016-03-11

    Stallion 900 Transit Buses Recalled for Wiper System Power Failure

    Stallion Bus is recalling 12 model year 2013 900 series transit buses because the wiper system may lose power, reducing visibility and increasing crash risk.

    Product
    STALLION — STALLION 900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V150000·2016-03-11

    Forest River Recalls Cargo Trailers With Incorrect Tire Pressure Labels

    Forest River is recalling specific Amera-Lite, Cargo Mate, Continental Cargo, and US Cargo trailers because incorrect tire pressure labels may lead to underinflation and tire failure.

    Product
    CARGO MATE — CARGO MATE, CONTINENTAL CARGO, AMERA-LITE CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16733·2016-03-11

    Room & Board Recalls Doyle Chairs Due to Laceration Hazard

    Room & Board is recalling Doyle arm and side chairs because the backrest can break during normal use, posing a laceration hazard.

    Product
    Doyle arm chairs and side chairs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·024-2016·2016-03-10

    Nestle Recalls Chicken Pizza and Lasagna Due to Glass Contamination

    Nestle USA is recalling specific chicken pizza and lasagna products due to possible glass contamination. No illnesses have been reported.

    Product
    Nestle USA, Inc. — Nestle USA Inc. Recalls Chicken Pizza And Chicken Lasagna Products Due To Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·16V146000·2016-03-10

    Mercedes-Benz Recalls 2016 GLC 300 Vehicles for Wiring Harness Defect

    Mercedes-Benz is recalling 2016 GLC 300 vehicles because a misrouted wiring harness may cause unexpected air bag deployment or engine stalling, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16731·2016-03-10

    Carlin Recalls Williamson and Thermoflo Furnaces and Boilers Due to Fire Hazard

    Carlin is recalling about 110 Williamson and Thermoflo furnaces and boilers equipped with Carlin oil burners because a wiring malfunction can cause the burners to fail to shut off, posing a fire hazard.

    Product
    Williamson-Thermoflo furnaces and boilers equipped with Carlin oil burners
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V145000·2016-03-10

    Hyundai Recalls 2016-2017 Santa Fe for Seat Belt Warning Defect

    Hyundai is recalling 34,200 Santa Fe vehicles because damaged wires may prevent the front seat belt warning light from activating, increasing crash injury risk.

    Product
    HYUNDAI — HYUNDAI SANTA FE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·16732·2016-03-10

    Anchor Industries Recalls Safety Pool Covers Due to Drowning Risk

    Anchor Industries is recalling specific safety pool covers because brass-plated snap hooks can break, posing a drowning risk. No injuries have been reported.

    Product
    Safety pool covers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0642-2016·2016-03-09

    Dole Recalls Spring Salad Mix From Springfield Ohio Facility

    Dole is withdrawing all Spring Salad Mix produced at its Springfield, Ohio facility due to a Class I recall. Affected products are sold nationwide and in Canada.

    Product
    Spring Salad Mix, 5 oz. bag, - Aldi; Walmart; 5 oz, and 10 oz. clamshell - Kroger; Dole - 3 lb. bag, 11 oz and 5 oz.. clamshell All marketed Dole and private label salads produced in the Springfield, OH facility. Product may be identified by an A in the upper right…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0656-2016·2016-03-09

    Dole Recalls Organic Baby Spinach and Salads from Springfield Facility

    Dole is withdrawing all salads produced in Springfield, Ohio, including organic baby spinach, due to a facility suspension.

    Product
    Organic Baby Spinach - 11 oz. and 5 oz. clamshell - Loblaw 5 oz and 16 oz, Clamshell - Kroger All marketed Dole and private label salads produced in the Springfield, OH facility. Product may be identified by an A in the upper right hand corner of the package.
    Category
    Food
    Distribution
    Distributed nationwide