The Recall Desk

State

Northern Mariana Islands product recalls

73,478 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 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22801–22825 of 73501

  • HighFDA (Devices)·Z-0207-2022·2021-11-17

    McKesson PREVENT HT Winged Blood Collection Needles Recall for Safety Mechanism Difficulty

    McKesson PREVENT HT Safety Winged Blood Collection Needles may have difficulty activating their safety mechanism. The recall affects units distributed nationwide.

    Product
    McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder, MFR # 16-NBCH21GS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0211-2022·2021-11-17

    QuikClot Combat Gauze Recalled for Potential Sterile Packaging Seal Failure

    Z-Medica is recalling 2400 units of QuikClot Combat Gauze due to potential packaging seal failures that could compromise sterile barrier integrity. Affected lot 12645 was distributed nationwide.

    Product
    QuikClot Combat Gauze-For Temporary External Use To Control Traumatic Bleeding Model / Part# 200
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0213-2022·2021-11-17

    Philips Azurion X-Ray Systems may lock up during simultaneous button presses

    Philips Azurion Interventional X-Ray Systems (software 2.1.x) may experience imaging lock-up when operators simultaneously press both the APC and Float Tabletop buttons.

    Product
    Philips Azurion Interventional Fluoroscopic X-Ray System, Software version 2.1.x, Model numbers 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222, 722223, 722224, 722225, 722226, 722227, 722228. (Azurion 3 M12, Azurion 3 M15, Azurion 5 M12, Azurion 5 M20, Azurion 7…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0205-2022·2021-11-17

    McKesson Safety Blood Collection Needles Recalled Over Safety Mechanism Activation Risk

    Nationwide recall of McKesson PREVENT HT Safety Blood Collection Needles (22G 1 1/4 inch) due to potential difficulty activating the safety mechanism. The protective feature may fail to engage properly during use.

    Product
    McKesson PREVENT HT Safety Blood Collection Needles, 22G 1 1/4 inch, MFR # 16-NBC22GS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0204-2022·2021-11-17

    McKesson Safety Blood Collection Needles Recalled for Safety Mechanism Defect

    McKesson PREVENT HT Safety Blood Collection Needles are being recalled due to potential difficulty in activating the safety mechanism. The recall affects needles distributed nationwide, including specific lot numbers with expiration dates through May 2025.

    Product
    McKesson PREVENT HT Safety Blood Collection Needles, 21G 1 1/4 inch, MFR # 16-NBC21GS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V889000·2021-11-17

    Toyota Recalls 2022 Sienna Models Due to Seat Belt Webbing Guide Defect

    Toyota is recalling 2022 Sienna and Sienna Hybrid vehicles with eight-passenger seating because an incorrect seat belt webbing guide may cause the belt to tear during a crash.

    Product
    TOYOTA — TOYOTA redundant SIENNA, SIENNA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0206-2022·2021-11-17

    McKesson PREVENT HT Blood Collection Needle Safety Mechanism Activation Issue

    McKesson PREVENT HT blood collection needles with specific lot numbers may have difficulty activating their safety mechanism. Healthcare facilities should contact the manufacturer for replacement guidance.

    Product
    McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder, MFR # 16-NBCH22GS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0215-2022·2021-11-17

    Hemodialysis Delivery System Software May Use Incorrect Treatment Parameters

    Baxter's Hemodialysis Delivery System may incorrectly revert to old prescription values when operators change prescriptions after filter changes, potentially resulting in incorrect treatment parameters.

    Product
    Hemodialysis Delivery System, Software Version 2.x.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0209-2022·2021-11-17

    Safety Blood Collection Needles Recalled Due to Safety Mechanism Activation Difficulty

    Henry Schein safety blood collection needles may have difficulty activating their safety mechanism, potentially increasing needlestick injury risk. Affected lots were distributed nationwide with expiration dates through late 2025.

    Product
    HENRY SCHEIN Safety Blood Collection Needle 22Gx 1 1/4 Inch, REF 570-2068, 100pcs/box 1000pcs/ctn 350*210*350mm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0231-2022·2021-11-17

    Tadalafil Tablets Recalled Due to Incorrect Product Formulation

    Sun Pharmaceutical is recalling Tadalafil Tablets USP 20 mg due to use of an incorrect grade of Crospovidone during manufacturing. The recall affects 36,786 bottles distributed to one distributor.

    Product
    TADALAFIL — TADALAFIL (TADALAFIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0230-2022·2021-11-17

    Tadalafil Tablets Recalled for Incorrect Product Formulation

    Sun Pharmaceutical Industries is recalling Tadalafil 5 mg tablets (Lot # DNC1127A) because an incorrect grade of Crospovidone was used during manufacturing. The product was distributed to one distributor who may have further distributed it nationwide.

    Product
    TADALAFIL — TADALAFIL (TADALAFIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0095-2022·2021-11-17

    Acetaminophen Oral Suspension Recalled Due to Contaminated Raw Ingredient

    Precision Dose Inc. is recalling Acetaminophen Oral Suspension (325 mg/10.15 mL) due to contaminated raw ingredient used in manufacturing. The recall affects 151,100 unit dose cups distributed nationwide for hospital use.

    Product
    ACETAMINOPHEN — ACETAMINOPHEN (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0094-2022·2021-11-17

    Acetaminophen Oral Suspension Recalled Due to Contaminated Raw Ingredient

    Precision Dose Inc. is recalling 166,920 unit dose cups of Acetaminophen Oral Suspension 160 mg/5 mL (Lot 503670) distributed nationwide due to cGMP deviations involving contaminated raw ingredient used in manufacturing.

    Product
    ACETAMINOPHEN — ACETAMINOPHEN (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V886000·2021-11-16

    Jayco Recalls 2020-2022 Motorhomes Due to Rear Suspension Fastener Defect

    Jayco is recalling 2020-2022 Anthem, Embark, Reatta, and Reatta XL motorhomes because rear suspension fasteners may loosen or break, increasing crash risk.

    Product
    ENTEGRA — ENTEGRA, JAYCO REATTA, REATTA XL, ANTHEM, redundant EMBARK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V885000·2021-11-16

    2021 Entegra Cornerstone Motorhome Power Steering Pump Defect Recall

    Jayco recalls certain 2021 Entegra Cornerstone motorhomes with a power steering pump defect that may result in loss of steering assist. Owners should contact Jayco for free pump replacement to prevent increased crash risk.

    Product
    ENTEGRA — ENTEGRA CORNERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V887000·2021-11-16

    EBY Generation Trailers Recalled for Missing Rear Conspicuity Tape

    M H Eby is recalling 2020-2022 EBY Generation trailers because missing white conspicuity tape on the top rear corners reduces visibility to other drivers.

    Product
    EBY — EBY GENERATION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V884000·2021-11-15

    Altec Recalls 2012-2016 Aerial Devices Due to Mounting Frame Cracks

    Altec is recalling 2012-2016 AT200A aerial devices because cracks in the mounting frame legs may cause the side plate to break, increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V880000·2021-11-12

    Chrysler Recalls 2019-2020 Ram Trucks for Fuel Pump Failure Risk

    Chrysler is recalling 2019-2020 Ram trucks with Cummins 6.7L diesel engines because the high-pressure fuel pump may fail, causing sudden engine stalls that increase crash risk.

    Product
    RAM — RAM 5500, 2500, 4500, 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V882000·2021-11-12

    Western Star Trucks Recalled for Electrical Arc Fire Risk

    Daimler Trucks North America is recalling 2017-2019 Western Star trucks because a power stud may contact the bulkhead, causing an electrical arc and increasing fire risk.

    Product
    WESTERN STAR — WESTERN STAR 4900, 5700, 4700, 6900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V881000·2021-11-12

    Volvo Recalls 2021 XC40 BEV Vehicles Due to Loose Engine Bolt

    Volvo is recalling 2021 XC40 BEV vehicles because a bolt securing the electrical motor bracket may be loose or missing, which could reduce structural protection in a crash.

    Product
    VOLVO — VOLVO XC40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V876000·2021-11-12

    2021-2022 Continental Cargo and Cargo Mate Trailers: Welding Defect in Coupler

    Forest River is recalling certain 2021-2022 Continental and Cargo Mate cargo trailers due to an improperly welded coupler. The defect may cause the trailer to separate from the tow vehicle, increasing crash risk.

    Product
    CARGO MATE — CARGO MATE, CONTINENTAL CARGO CARGO TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V878000·2021-11-12

    Alfa Romeo Stelvio and Giulia fuel line sensor housing cracks

    The fuel line sensor housing in certain 2020-2021 Alfa Romeo Stelvio and Giulia vehicles may crack and leak fuel, causing engine stalls and increasing fire risk.

    Product
    ALFA ROMEO — ALFA ROMEO STELVIO, GIULIA
    Category
    Vehicle
    Distribution
    Distributed nationwide