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.

58326–58350 of 73856

  • HighNHTSA·14V263000·2014-05-16

    Nissan Recalls 2014 LEAF Vehicles Due to Inverter Failure Risk

    Nissan is recalling 2014 LEAF vehicles because a motor control circuit board defect may cause the inverter to fail, leading to an unexpected vehicle shut down.

    Product
    NISSAN — NISSAN LEAF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateUSDA FSIS·029-2014·2014-05-16

    Transatlantic Foods Recalls Pork Products Due to Misbranding

    Transatlantic Foods is recalling 449,000 pounds of pork products because labels falsely claimed the items contained no antibiotics.

    Product
    Recall Notification Report 029-2014 (Pork Products)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·14179·2014-05-15

    Gree Recalls Dehumidifiers Due to Fire and Burn Hazards

    Gree is recalling approximately 2.5 million dehumidifiers in the U.S. and 55,000 in Canada due to fire and burn hazards. Consumers should unplug the units and contact Gree for a refund.

    Product
    Dehumidifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·14184·2014-05-15

    Exmark Recalls Quest ZRT Riding Mowers Due to Steering Failure

    Exmark is recalling 2009 and 2010 Quest ZRT riding mowers because the steering assembly can fail, causing loss of control and crash hazards.

    Product
    Exmark Quest ZRT Riding Mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V253000·2014-05-15

    GM Recalls 2014 Cadillac CTS for Windshield Wiper Failure Risk

    General Motors is recalling 2014 Cadillac CTS vehicles because the windshield wipers may stop working after a jump start, increasing crash risk.

    Product
    CADILLAC — CADILLAC CTS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14182·2014-05-15

    StyleCraft Recalls Upholstered Benches Due to Fall Hazard

    StyleCraft is recalling upholstered benches sold at HomeGoods because they can crack and break, posing a fall hazard. No injuries have been reported.

    Product
    Upholstered Benches
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14180·2014-05-15

    H&M Recalls Girls' Leggings Due to Choking Hazard

    H&M is recalling approximately 65,000 girls' leggings because a metal part on the belt can detach, posing a choking hazard to young children.

    Product
    Girls' Leggings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14183·2014-05-15

    BMC Recalls Three Bicycle Models Due to Fork Breakage Hazard

    BMC is recalling approximately 160 Alpenchallenge, Masschallenge, and Urbanchallenge bicycles because the carbon forks can crack or break, posing a fall hazard.

    Product
    BMC Alpenchallenge, Masschallenge and Urbanchallenge Bicycles with Aprebic Forks
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1308-2014·2014-05-14

    Mangiacotti Ginger Lime Hand Sanitizer Recalled for Bacterial Contamination

    Mangiacotti is recalling Ginger Lime Hand Sanitizer Spray due to elevated counts of Serratia liquefaciens bacteria.

    Product
    Mangiacotti - Ginger Lime Hand Sanitizer Spray, alcohol free, 0.5 fl Oz. 15 mL spray bottle, UPC 870678005351, Active Ingredient Benzalkonium Chloride 0.1%, Dist By: Mangiacotti, Attleboro, MA 02703.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1541-2014·2014-05-14

    Med-Mizer Retractabed Recall for Insufficient Welding on Foot Cross Tube

    Med-Mizer is recalling 191 Retractabed Clinical Contour adjustable beds manufactured before June 7, 2008, due to insufficient welding that could cause bed collapse.

    Product
    RetractaBed , Clinical Contour, Med - Mizer Inc..... Model SS 762 ( 76 " bed w/ 2 motors); 763 (3 motors); 763 A ( 3 motors, autocontour) 120 V, ...Max Safe Working Load 450 LBS. Acute/Longterm Care AC Powered Adjustable Bed for geriatric care.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V246000·2014-05-14

    GM Recalls 2014-2015 Trucks and SUVs for Steering Defect

    General Motors is recalling specific 2014 Chevrolet Silverado, 2014 GMC Sierra, and 2015 Chevrolet Tahoe vehicles because the steering tie rod may not be properly tightened, risking loss of steering.

    Product
    GMC — GMC, CHEVROLET SIERRA, SILVERADO, TAHOE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1542-2014·2014-05-14

    Med-Mizer RetractaBed Recall for Insufficient Welding on Foot Cross Tube

    Med-Mizer is recalling RetractaBed Clinical Contour adjustable beds due to insufficient welding on the foot cross tube, which may cause bed collapse or rollers to detach.

    Product
    RetractaBed , Clinical Contour, Med - Mizer Inc..... Model SS 799, 120 V, ...Max Safe Working Load 450 LBS. Acute/Longterm Care AC Powered Adjustable Bed for geriatric care.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1546-2014·2014-05-14

    Alere INRatio2 Test Strips Recalled for Inaccurate INR Results

    Alere San Diego, Inc. is recalling INRatio2 PT/INR Professional Test Strips because they may report inaccurately low INR results, potentially affecting warfarin therapy monitoring.

    Product
    Alere INRatio2 PT/INR Professional Test Strips, Model Number: 99008G2. The Alere INRatio2 PT/INR Monitoring System (Professional Use), consisting of the Monitor and test strip, is used for quantitative determination of international normalized ratio (INR) in fresh, capillary…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V252000·2014-05-14

    GM Recalls 2004-2012 Vehicles for Electronic Stability Control Defect

    General Motors is recalling 2004-2012 Chevrolet, Pontiac, and Saturn vehicles because a wiring issue can disable crash avoidance features like traction control.

    Product
    CHEVROLET — CHEVROLET, SATURN, PONTIAC MALIBU, AURA, G6, MALIBU MAXX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V255000·2014-05-14

    Lodal Recalls 2011-2013 Evo Garbage Trucks Due to Fire Risk

    Lodal is recalling 2011-2013 Evo garbage trucks because condensation in the intake manifold may freeze, causing sensor issues that increase the risk of vehicle fire or burn injury.

    Product
    LODAL — LODAL EVO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1543-2014·2014-05-14

    Med-Mizer RetractaBed Recall Due to Insufficient Welding on Foot Cross Tube

    Med-Mizer is recalling 2,980 RetractaBed Clinical Contour adjustable beds due to insufficient welding on the foot cross tube, which may cause bed collapse.

    Product
    RetractaBed , Clinical Contour, Med - Mizer Inc..... Model SS 801, 802, 803, 803A: 80 " bed with 1, 2, or 3, motors and autocontour 120 V, ...Max Safe Working Load 450 LBS. Acute/Longterm Care AC Powered Adjustable Bed for geriatric care.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1565-2014·2014-05-14

    SpineFrontier S-Lift Lock Shaft Inserter Recalled for Potential Breakage

    SpineFrontier is recalling S-Lift Lock Shaft Inserters because the impact cap or pin may break during spinal surgery, potentially releasing fragments into the sterile field.

    Product
    SpineFrontier S-Lift Lock Shaft Inserter, an instrument used with S-LIFT Intervertebral Body Fusion Device in spinal fusion surgery. Product Usage: The S-Lift Lock Shaft SI50001 mates with SI50002, Implant Inserter, to aid in securing the implant to the whole implant inserter…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V247000·2014-05-14

    GM Recalls 2014 Chevrolet Malibu for Brake Vacuum Assist Loss

    General Motors is recalling specific 2014 Chevrolet Malibus because a software issue may cause a complete loss of brake vacuum assist, increasing stopping distance.

    Product
    CHEVROLET — CHEVROLET MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1553-2014·2014-05-14

    Siemens ADVIA Centaur XP Immunoassay System Recalled for Gas Spring Failure

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur XP Immunoassay systems because gas springs may fail, causing the instrument cover to fall.

    Product
    ADVIA Centaur XP Immunoassay system, an automated in vitro diagnostic analyzer. Catalog # 078-A011-03 - ADVIA Centaur XP, Catalog # 078-A011R03 - ADVIA Centaur XP refurb.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1306-2014·2014-05-14

    Mangiacotti Clementine Hand Sanitizer Spray Recalled for Bacterial Contamination

    Mangiacotti is recalling Clementine Hand Sanitizer Spray due to elevated counts of Serratia liquefaciens bacteria.

    Product
    Mangiacotti - Clementine Hand Sanitizer Spray, alcohol free, 0.5 fl Oz. 15 mL spray bottle, UPC 870678005337, Active Ingredient Benzalkonium Chloride 0.1%, Dist By: Mangiacotti, Attleboro, MA 02703.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1564-2014·2014-05-14

    Siemens ADVIA Centaur Folate Assay Recalled for Potential Out-of-Range Results

    Siemens Healthcare Diagnostics is recalling specific lots of the ADVIA Centaur Folate assay because serum controls may go out of range low and whole blood patient results may shift.

    Product
    Siemens ADVIA Centaur Folate Cat No. 06891541 SMN 10325366 (500 tests) Cat No. 06367974 SMN 10310308 (100 tests) Cat No. 00203473 SMN 10331250 (Ref) (500 tests) Cat No. 09132781 SMN 10340209 (Ref) (2500 tests) For in vitro diagnostic use in the quantitative determination…
    Category
    Medical Device
    Distribution
    Distributed nationwide