The Recall Desk

State

Northern Mariana Islands product recalls

72,907 recalls have nationwide distribution and so reach Northern Mariana Islands. 22 additional recalls listed Northern Mariana Islands specifically in their distribution scope.

What the numbers show

Total
22
Critical
0
Severe
8
Most recent
2025-02-05

Of the 22 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 8 (36%) are Severe.

Which agencies issued them

These figures cover only the 22 recalls whose distribution notice names Northern Mariana Islands specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1301–1325 of 72929

  • HighFDA (Devices)·Z-2347-2026·2026-06-17

    MIC Safety 14 Fr push PEG kits contain recalled lidocaine injection

    MIC Safety PEG Kits with ENFit Connectors, 14 Fr PUSH OTW, catalog number 8170-14, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall.

    Product
    Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PUSH OTW Model/Catalog Number: 8170-14 Product Description: Feeding Tube Kit Component: No
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2339-2026·2026-06-17

    CORFLO Safety PEG kit 50-6312 contains recalled lidocaine injection

    CORFLO Safety PEG Kits with ENFit Connector, catalog number 50-6312, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 43 kits affected.

    Product
    Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-6312
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0586-2026·2026-06-17

    Zep alcohol sanitizer spray drums recalled for microbial contamination

    Zep Alcohol Sanitizer Spray, ethanol 70%, in 55-gallon drums is being recalled for microbial contamination. Five drums are affected.

    Product
    Zep, Alcohol Sanitizer Spray, Ethanol 70%, Net Contents 55 Gallons 208 Liters, Made in USA, A Zep Inc. Brand, Distributed by: Zap Inc., 350 Joe Frank Harris Parkway, SE, Emerson, GA 30137, NDC 66949-133-85.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2314-2026·2026-06-17

    GE Allia IGS 3 Pulse systems pose shock risk to servicers

    Allia IGS 3 Pulse angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on. Nine units affected.

    Product
    Allia IGS 3 Pulse angiographic X-ray system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2410-2026·2026-06-17

    Halyard eye bag packs shipped without validated sterilization in Iowa

    Halyard Eye Bag Packs, kit code UIEB48-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 60 kits affected.

    Product
    Halyard, Eye Bag Pack. Kit Code: UIEB48-01.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2344-2026·2026-06-17

    MIC Safety 14 Fr pull PEG kits contain recalled lidocaine injection

    MIC Safety PEG Kits, 14 Fr PULL, catalog number 7180-14, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 208 kits affected.

    Product
    Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PULL Model/Catalog Number: 7180-14
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2312-2026·2026-06-17

    Plum Duo infusion pumps may not display soft limit alerts

    Plum Duo Infusion Pumps are being recalled because under certain conditions the pump may not display a soft limit alert before delivery starts, potentially leading to under- or over-delivery.

    Product
    Plum Duo Infusion Pump, 40002-0401
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2341-2026·2026-06-17

    MIC Safety 7170-14 push PEG kits contain recalled lidocaine injection

    MIC Safety PEG Kits, 14 Fr PUSH OTW, catalog number 7170-14, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 22 kits affected.

    Product
    Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW Model/Catalog Number: 7170-14 Product Description: Feeding Tube Kit
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2398-2026·2026-06-17

    Siemens Dimension tacrolimus reagent cartridges may bias results positively

    Three lots of the Siemens Dimension Tacrolimus Flex reagent cartridge are being recalled because of a potential positive bias in quality control and patient sample results.

    Product
    Siemens Dimension Tacrolimus Flex Reagent Cartridge (TAC), REF DF207, SMN 10700795; enzyme immunoassay
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2352-2026·2026-06-17

    MIC Safety 24 Fr pull ENFit PEG kits contain recalled lidocaine

    MIC Safety PEG Kits with ENFit Connectors, 24 Fr PULL, catalog number 8180-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall.

    Product
    Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PULL Model/Catalog Number: 8180-24
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2322-2026·2026-06-17

    TDC VELOCE 23 gauge vitrectomy cutters may have loose outer knife

    TDC VELOCE 23G Two Dimensional Cutters are being recalled following an increase in complaints of a loose outer knife, including reports of it loosening during use.

    Product
    TDC VELOCE", 23G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT23, 9311.23G01, 9311.23G02, 9311.23K01, 9311.23K02, 9311.23K03, 9623.G0201, 9623.G0202, 9623.K0201, 9311.23G01-00;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2413-2026·2026-06-17

    Orca single use endoscope valves recalled over sticking suction buttons

    Boston Scientific is removing Orca Sterile, Single Use Air/Water and Suction Valves because of a higher than anticipated occurrence of the suction button sticking. 9,750 units affected.

    Product
    Orca Single Use Air/Water and Suction Valves, Material Number (UPN) SUV-617-50; The Orca Air/Water Valve is intended to be used to control the air/water function on an endoscope during a GI (gastrointestinal) endoscopic procedure.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2345-2026·2026-06-17

    MIC Safety 20 Fr pull PEG kits contain recalled lidocaine injection

    MIC Safety PEG Kits, 20 Fr PULL, catalog number 7180-20, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 3,184 kits affected.

    Product
    Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PULL Model/Catalog Number: 7180-20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2351-2026·2026-06-17

    MIC Safety 20 Fr PEG kits contain recalled lidocaine injection

    MIC Safety PEG Kits with ENFit Connectors, 20 Fr PULL, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall for quality issues. 6,005 kits affected.

    Product
    Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PULL Model/Catalog Number: 8180-20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·H-0940-2026·2026-06-17

    Park St. Deli macaroni and cheese does not declare soy

    Park St. Deli Macaroni & Cheese, 20 oz, is being recalled because of undeclared soy lecithin. The action covers 58,405 cases.

    Product
    Park St. Deli Macaroni & Cheese, NET WT 20 OZ (1 LB 4 OZ) 567g, product packed in plastic tub and placed into paperboard sleeve. 9/20 oz packages per case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2330-2026·2026-06-17

    CGuard Prime 10mm by 40mm carotid stents may fail deployment

    CGuard Prime Carotid Stent Systems, 135 cm with a 10 mm x 40 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.

    Product
    CGuard¿ Prime Carotid Stent System, 135cm, 10mmx40mm Model/Catalog Number: CND1040
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2404-2026·2026-06-17

    Boston Scientific Clik X anchors may lack sterility assurance

    Boston Scientific Clik X Anchors, model SC-4318, are being recalled because the sterile anchors may lack sterility assurance. 43 units are affected.

    Product
    Boston Scientific Model SC-4318, Clik X Anchor REF: M365SC43180
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2338-2026·2026-06-17

    CORFLO Safety PEG kit 50-5320 contains recalled lidocaine injection

    CORFLO Safety PEG Kits with ENFit Connector, catalog number 50-5320, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 72 kits affected.

    Product
    Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-5320
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2400-2026·2026-06-17

    Aluminum chloride hemostatic gel kits shipped with wrong package insert

    Advance Aluminum Chloride Gel Clear Hemostatic Gel Kits are being recalled because some units contain the package insert for Ferric Sulfate Gel, which gives different first aid instructions.

    Product
    Advance Aluminum Chloride Gel Clear Hemostatic Gel Kit, Catalog number 504600-28
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2409-2026·2026-06-17

    Halyard drape packs shipped without undergoing validated sterilization process

    Halyard Drape Packs, kit code LMDP36-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 72 kits affected.

    Product
    Halyard, Drape Pack. Kit Code: LMDP36-01.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2311-2026·2026-06-17

    Plum Solo Precision IV pumps may not display soft limit alerts

    Plum Solo Precision IV Pumps are being recalled because under certain conditions the pump may not display a soft limit alert before delivery starts, potentially leading to under- or over-delivery.

    Product
    Plum Solo Precision IV Pump, 40001-0401
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2325-2026·2026-06-17

    CGuard Prime 8mm by 30mm carotid stents may fail deployment

    CGuard Prime Carotid Stent Systems, 135 cm with an 8 mm x 30 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.

    Product
    Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx30mm Model/Catalog Number: CND0830
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2324-2026·2026-06-17

    TDC VELOCE 27 gauge vitrectomy cutters may have loose outer knife

    TDC VELOCE 27G Two Dimensional Cutters are being recalled following an increase in complaints of a loose outer knife, including reports of it loosening during use.

    Product
    TDC VELOCE", 27G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT27, 9311.27G01, 9311.27G02, 9311.27K01, 9311.27K02, 9311.27K03, 9627.G0101, 9627.G0201, 9311.27G01-00;
    Category
    Medical Device
    Distribution
    Distributed nationwide