The Recall Desk

State

Northern Mariana Islands product recalls

73,584 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 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27726–27750 of 73607

  • HighCPSC·20774·2020-09-03

    StoreYourBoard Recalls Hi-Lift Storage Hoists Due to Strap Breakage Hazard

    StoreYourBoard.com is recalling Hi-Lift Storage Hoists because green polypropylene straps can break, causing stored items to fall and potentially injure passersby.

    Product
    Hi-Lift Storage Hoist Classic and Pro models sold with green polypropylene straps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20775·2020-09-03

    SODA SENSE Recalls CO2 Canisters Due To Valve Ejection Injury Hazard

    SODA SENSE is recalling about 19,200 CO2 canisters because a valve can break and eject, posing an injury hazard. No injuries have been reported, but minor property damage has occurred.

    Product
    SODA SENSE® CO2 canisters
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V539000·2020-09-03

    Western Star and Freightliner trucks recalled for suspension hardware defect

    Daimler Trucks recalls 2020-2021 Western Star 4700 and 4900, and Freightliner 114SD and 122SD trucks due to suspension axle hardware that may be insufficiently long to engage locking nuts, creating road hazards and crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR 122SD, 4900, 114SD, 4700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V537000·2020-09-03

    2021 Chevrolet Trailblazer and 2020 Buick Encore GX Seat Fastener Recall

    General Motors is recalling 2021 Chevrolet Trailblazers and 2020 Buick Encore GX vehicles because front seat rear attachment bolts may not have been installed, potentially allowing seats to move during a crash.

    Product
    BUICK — BUICK, CHEVROLET ENCORE, TRAILBLAZER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1274-2020·2020-09-02

    Thomson International Recalls White Onions Linked to Salmonella Outbreak

    Thomson International is recalling white onions packed under Thomson Premium, Onions 52, and El Competitor brands due to a link to a Salmonella Newport outbreak.

    Product
    White onions; Packed under brand names of Thomson Premium, Onions 52, El competitor. Thomson Premium: 25 lb. mesh sack -No UPC 50 lb. mesh sack -No UPC Onions 52: 8 lb. mesh bag - UPC 8 15222 01019 1 El Competitor 50 lb. mesh sack - No UPC
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1272-2020·2020-09-02

    Red Onions Recalled Due to Salmonella Newport Outbreak Investigation

    Thomson International is recalling red onions nationwide and in Canada because a traceback investigation linked them to a Salmonella Newport outbreak.

    Product
    Red onions; Packed under brand names of Thomson Premium, Onions 52, Utah Onions, Harley's Best, Onions 52, Imperial Fresh, TLC Thomson International, El Competidor Thomson Premium packed in 50 and 25 lb.mesh sack, and 2 lb. mesh sack - UPC 33383 60101 3 lb. mesh sack…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1534-2020·2020-09-02

    Medichem Recalls Chlorhexidine Gluconate Due to Serratia marcescens Contamination

    Medichem S.A. is recalling Chlorhexidine Gluconate 0012 for manufacturing due to microbial contamination with Serratia marcescens.

    Product
    Chlorhexidine Gluconate 0012 For Manufacturing, Processing or Repacking, RX Only, Medichem, S.A. Poligono Industrial Celra, 17460, Celra, Girona (Spain/Espana); Fructuos Gelabert, 6-8, 08970, Sant Joan Despi, Barcelona (Spain/Espana) NDC 53296-0012-0
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1273-2020·2020-09-02

    Thomson International Recalls Yellow Onions Linked to Salmonella Outbreak

    Thomson International is recalling yellow onions nationwide and in Canada after a traceback investigation linked red onions to a Salmonella Newport outbreak.

    Product
    Yellow onions; Packed under brand names of Onions 52, Majestic, Hartley's Best, Kroger, Food Lion, Thomson Premium, TLC Thomson International, El competitor, Tender Loving Care, Imperial Fresh. Onions 52: 10 lb. mesh sack - UPC 33383 60004 3 lb. mesh sack - UPC 33383 60002…
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1552-2020·2020-09-02

    SCA Pharmaceuticals Recalls Heparin Sodium Injection Due to Cross Contamination

    SCA Pharmaceuticals is recalling Heparin Sodium 5,000 units in 0.9% Sodium Chloride 1000 mL single-dose containers due to cross-contamination with undeclared benzyl alcohol.

    Product
    Heparin Sodium 5,000 units in 0.9% Sodium Chloride 1000 mL, Single Dose Container, Rx Only Injection for Intravenous Use (5 units/mL), SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC#: 70004-0650-46, Bar Code 70004065046.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1551-2020·2020-09-02

    SCA Pharmaceuticals Recalls Heparin Sodium Injection Due to Cross Contamination

    SCA Pharmaceuticals is recalling 366 containers of Heparin Sodium 5,000 units in 0.9% Sodium Chloride 500 mL due to cross-contamination with undeclared benzyl alcohol.

    Product
    Heparin Sodium 5,000 units in 0.9% Sodium Chloride 500 mL, Single Dose Container, Rx Only Injection for Intravenous Use (10 units/mL), SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC#: 70004-0650-44, Bar Code 70004065044.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1275-2020·2020-09-02

    Thomson International Recalls Sweet Yellow Onions Linked to Salmonella Outbreak

    Thomson International is recalling Sweet Yellow onions after a traceback investigation linked red onions to a Salmonella Newport outbreak.

    Product
    Sweet Yellow onions; Packed under brand names of Thomson Premium, TLC Thomson International. Thomson Premium: 50 lb. mesh sack -No UPC TLC Thomson International; 40 lb. Carton - No UPC
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1553-2020·2020-09-02

    SCA Pharmaceuticals Recalls Heparin Sodium Injection Due to Cross Contamination

    SCA Pharmaceuticals is recalling Heparin Sodium 10,000 units injection containers due to cross contamination with undeclared benzyl alcohol and missing parabens.

    Product
    Heparin Sodium 10,000 units in 0.9% Sodium Chloride 1000 mL, Single Dose Container, Rx Only Injection for Intravenous Use (10 units/mL), SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC#: 70004-0652-46, Bar Code 70004065246.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V531000·2020-09-02

    Gulf Stream Enlighten Travel Trailer Recall for Refrigerator Seal Defect

    Gulf Stream is recalling 2020 Enlighten travel trailers because a missing refrigerator trim strip may allow carbon monoxide or flammable gas to enter the living area.

    Product
    GULF STREAM — GULF STREAM ENLIGHTEN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1544-2020·2020-09-02

    Bayshore Pharmaceuticals Recalls Metformin Hydrochloride Tablets Due to CGMP Deviations

    Bayshore Pharmaceuticals is voluntarily recalling 3,984 bottles of Metformin Hydrochloride Extended-Release Tablets due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    METFORMIN HYDROCHLORIDE — METFORMIN HYDROCHLORIDE (METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1537-2020·2020-09-02

    Fresenius Kabi Recalls Dexmedetomidine Injection Due to Lidocaine Contamination

    Fresenius Kabi is recalling specific lots of Dexmedetomidine HCl Injection due to trace amounts of lidocaine contamination.

    Product
    Dexmedetomidine HCl in 0.9% Sodium Chloride Injection, 200 mcg per 50 mL (4 mcg per mL), for intravenous infusion, preservative free, 50 mL Single Dose Bottle, Rx only, Fresenius Kabi Lake Zurich, IL 60047, NDC 63323-671-05
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2880-2020·2020-09-02

    Biosense Webster Recalls CARTO 3 System Software Due to Defect

    Biosense Webster is recalling the CARTO 3 System software due to a defect that may cause tag sites to disappear, potentially leading to cardiac perforation.

    Product
    CARTO 3 System (Software Version V7.1.80), CARTO VISITAG Module - Product Usage: FGThe intended use of the system is catheter-based cardiac electrophysiological (EP) procedures. The system provides information about the electrical activity of the heart and about catheter…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2831-2020·2020-09-02

    Datascope Intra-Aortic Balloon Catheters Recalled for Potential Endotoxin Contamination

    Datascope Corporation is recalling specific lots of Intra-Aortic Balloon Catheters due to potential endotoxin contamination. The recall affects 1,275 kits distributed worldwide.

    Product
    Datascope Intra-Aortic Ballon Catheters (IABs)-MEGA 7.5Fr 30cc IAB, P/N: 0684-00-0294-01,0684-00-0294-01U, 0684-00-0294-02, 0684-00-0294-02U- Product Usage: Indications For Use: Acute Coronary Syndrome Cardiac and Non-Cardiac Surgery Complications of Heart Failure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1550-2020·2020-09-02

    SCA Pharmaceuticals Recalls Heparin Sodium Injection Due to Cross-Contamination

    SCA Pharmaceuticals is recalling Heparin Sodium 2,500 units injection containers that contain undeclared benzyl alcohol and lack declared parabens.

    Product
    Heparin Sodium 2,500 units in 0.9% Sodium Chloride 500 mL, Single Dose Container, Rx Only Injection for Intravenous Use (5 units/mL), SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC#: 70004-0655-44, Bar Code 70004065544.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V534000·2020-09-02

    Tiffin Recalls 2020 Bus and Phaeton Motorhomes for Steering Bolt Issue

    Tiffin Motorhomes is recalling 2020 Bus and Phaeton models because steering pinch bolts may not be properly tightened, which could lead to a loss of steering control.

    Product
    TIFFIN — TIFFIN BUS, PHAETON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1535-2020·2020-09-02

    Aurobindo Recalls Sulfamethoxazole and Trimethoprim Tablets Due to Metal Wire

    Aurobindo Pharma USA Inc. is recalling specific lots of Sulfamethoxazole and Trimethoprim tablets because of reports of metal wire in the tablets.

    Product
    SULFAMETHOXAZOLE AND TRIMETHOPRIM — SULFAMETHOXAZOLE AND TRIMETHOPRIM (SULFAMETHOXAZOLE AND TRIMETHOPRIM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1543-2020·2020-09-02

    Bayshore Pharmaceuticals Recalls Metformin Hydrochloride Tablets Due to CGMP Deviations

    Bayshore Pharmaceuticals is voluntarily recalling 594 bottles of Metformin Hydrochloride Extended-Release Tablets due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    METFORMIN HYDROCHLORIDE — METFORMIN HYDROCHLORIDE (METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighCPSC·20174·2020-09-02

    IMMI Recalls UTV Harnesses Due to Missing Stitching Injury Hazard

    IMMI is recalling about 162,000 SubZero and Click6 UTV harnesses because missing stitching may prevent proper restraint during a crash. No injuries have been reported.

    Product
    IMMI SubZero 4-point and IMMI Click6 6-point UTV harnesses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V536000·2020-09-02

    Volvo commercial trucks recalled for brake pedal failure risk

    Volvo Trucks is recalling 2020-2021 commercial trucks because the brake pedal may dislodge, making brakes inoperable. Affected models: VHD, VAH, VNL, and VNR.

    Product
    VOLVO — VOLVO VNL, VNR, VAH, VHD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V535000·2020-09-02

    2021 Volvo trucks recalled for potentially loose steering king pin nuts

    Volvo Trucks is recalling certain 2021 VHD, VNL, and VNR vehicles because the king pin nut may not have been properly installed during axle assembly, which could cause the axle knuckle to separate and increase crash risk.

    Product
    VOLVO — VOLVO VHD, VNL, VNR
    Category
    Vehicle
    Distribution
    Distributed nationwide