The Recall Desk

State

Northern Mariana Islands product recalls

73,509 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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24826–24850 of 73532

  • HighFDA (Devices)·Z-1664-2021·2021-05-26

    Bard Access Systems Recalls Groshong NXT ClearVue Catheters Due to Connector Defects

    Bard Access Systems is recalling specific lots of Groshong NXT ClearVue Catheters because connector defects may prevent proper catheter passage or locking.

    Product
    REF 69655405, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Basic Kit, 4F, Single-Lumen, TLS, UDI: (01)10801741147521 - Product Usage: is designed for use when central venous catheterization is prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1661-2021·2021-05-26

    Bard Groshong NXT ClearVue Catheter Recall for Connector Defects

    Bard Access Systems is recalling Groshong NXT ClearVue Catheters due to defects in the distal connector that may prevent proper catheter passage or locking.

    Product
    REF 9617408, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Full Kit, 4F, Single-Lumen, TLS, UDI: (01)10801741036009 - Product Usage: is designed for use when central venous catheterization is prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0542-2021·2021-05-26

    Bloommy Biotin Collagen Keratin Capsules Recalled for Undeclared Fish

    Bloommy Inc. is recalling Biotin Collagen Keratin Capsules because they contain undeclared fish collagen, a potential allergen.

    Product
    "Bloomy*** Biotin Collagen Keratin***Capsules for SKIN, JOINT, HAIR***Supplement Facts***Marine Collagen***Manufactured for Bloommy Inc. 106 W. Broad St. Pawcatuck, CT 06379"
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1655-2021·2021-05-26

    Bard Groshong Catheter Recall for Connector Defects

    Bard Access Systems is recalling specific lots of Groshong NXT ClearVue Catheters due to connector defects that may prevent proper catheter passage or locking.

    Product
    REF 7617408D, Groshong NXT ClearVue Catheter, Maximal Barrier Kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741035262 - Product Usage: is designed for use when central venous catheterization is prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V397000·2021-05-26

    2021 KZRV SPORTTREK and STRATUS trailers water heater circuit fire hazard

    KZRV is recalling 2021 SPORTTREK and STRATUS trailers with incorrectly sized water heater circuit breakers. The wiring defect may prevent proper electrical protection and increase fire risk.

    Product
    KZRV — KZRV SPORTTREK, STRATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21141·2021-05-26

    Target Recalls Room Essentials Shower Stools Due to Fall Hazard

    Target is recalling Room Essentials Shower Stools because they can become unstable or slippery, posing a fall hazard. About 58,500 units were sold.

    Product
    Room Essentials Shower Stools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1596-2021·2021-05-26

    Roche Recalls Troponin I Immunoassay Kits Due to False Negative Risk

    Roche Diagnostics is recalling 726 Elecsys Troponin I Immunoassay kits because they may produce false negative results when run immediately after proBNP II tests on specific modules.

    Product
    Elecsys Troponin I Immunoassay: Catalog# 05094810160 - Product Usage: intended to aid in the diagnosis of myocardial infarction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21139·2021-05-26

    Ergobaby Recalls METROUS Strollers Due to Choking Hazard

    Ergobaby is recalling METROUS strollers because a harness buckle button can break and detach, posing a choking hazard to young children.

    Product
    METROUS1, METROUS2 and METROUS4 Compact City Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1669-2021·2021-05-26

    Bard Groshong NXT ClearVue Catheter Recall for Connector Defects

    Bard Access Systems is recalling specific lots of Groshong NXT ClearVue Catheters due to connector defects that may prevent proper catheter passage or locking.

    Product
    REF 7617407, Groshong NXT ClearVue Catheter, Full Kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741035248 - Product Usage: is designed for use when central venous catheterization is prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0537-2021·2021-05-26

    PepsiCo Recalls Evolve Protein Shakes Due to Undeclared Soy

    PepsiCo is recalling Evolve Double Chocolate Plant-Based Protein Shakes because they contain undeclared soy. The recall covers 17,381 cases distributed nationwide.

    Product
    Evolve Double Chocolate Plant-Based Protein Shake, 11oz "Tetra Pak" carton, sold 4 cartons per retail unit. UPC on retail 4 pack: 876063007887 Packed 3 retail four packs per wholesale case.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1646-2021·2021-05-26

    Biopsybell Cement Delivery Kits Recalled for Potential Sterility Failure

    Biopsybell is recalling 305 units of 10 Gauge Single Cement Delivery kits because they were labeled sterile but may not have been sterilized.

    Product
    10 GAUGE SINGLE CEMENT DELIVERY 4 FILLERS 4 SYRINGES, CODE INTVM-SCDK
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1666-2021·2021-05-26

    Bard Groshong NXT ClearVue Catheter Recall for Connector Defects

    Bard Access Systems is recalling specific Groshong NXT ClearVue Catheters because connector defects may prevent proper catheter passage or locking.

    Product
    REF CK000379, Groshong NXT ClearVue Catheter with Sherlock Tip Location System (TLS) Stylet, Full Kit, 4F, Single-Lumen, TLS, CE 2797, UDI: (01)10801741102704 - Product Usage: is designed for use when central venous catheterization is prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1657-2021·2021-05-26

    Bard Groshong NXT ClearVue Catheter Recalled for Connector Defects

    Bard Access Systems is recalling Groshong NXT ClearVue Catheters because connector defects may prevent proper catheter passage or locking.

    Product
    REF 7655405J, Groshong NXT ClearVue Catheter, Basic Kit, 4F, Single-Lumen, 60 cm, UDI: (01)10801741200615 - Product Usage: is designed for use when central venous catheterization is prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1667-2021·2021-05-26

    Bard Access Systems Recalls Groshong NXT ClearVue Catheters Due to Connector Defects

    Bard Access Systems is recalling specific lots of Groshong NXT ClearVue Catheters because connector defects may prevent proper catheter passage or locking.

    Product
    REF CK000516, Groshong NXT ClearVue Catheter with Sherlock 3CG Tip Positioning System (TPS) Stylet, Full Kit, 4F, Single-Lumen, TPS, CE 2797, UDI: (01)10801741107891 - Product Usage: is designed for use when central venous catheterization is prescribed.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V395000·2021-05-26

    2017–2021 Holiday Rambler and Fleetwood Motorhomes Recalled for Improperly Sealed Flooring

    REV Recreation Group is recalling 2017–2021 Fleetwood, Holiday Rambler, and Fleetwood motorhomes with improperly sealed floor holes that could allow carbon monoxide into the living area. Dealers will reseal the floor free of charge.

    Product
    HOLIDAY RAMBLER — HOLIDAY RAMBLER, FLEETWOOD VACATIONER, BOUNDER, SOUTHWIND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V394000·2021-05-26

    Pierce Recalls 2017-2021 Commercial Vehicles Due to Fuel Rail Leak Risk

    Pierce Manufacturing is recalling 2017-2021 Arrow XT, Enforcer, Impel, Quantum, Saber, and Velocity vehicles because a sealing washer defect may cause high-pressure fuel leaks, increasing fire risk.

    Product
    PIERCE — PIERCE ARROW XT, ENFORCER, VELOCITY, IMPEL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1650-2021·2021-05-26

    Medtronic Recalls Two Defective Implantable Cardioverter Defibrillators

    Medtronic is recalling two Cobalt HF Quad MRI SureScan CRT-D devices due to a potential missing resistance spot weld.

    Product
    Cobalt HF Quad MRI SureScan Implantable Cardioverter Defibrillators with Cardiac Resynchronization Therapy (CRT-D) - Product Usage: are multiprogrammable cardiac devices that monitor and regulate a patient s heart rate by providing single- or dual chamber rate responsive…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1595-2021·2021-05-26

    Roche Recalls Troponin I STAT Immunoassay Kits Due to False Negative Risk

    Roche Diagnostics is recalling 10,489 Troponin I STAT Immunoassay kits because they may produce false negative results when run after proBNP II tests on specific modules.

    Product
    Elecsys Troponin I STAT Immunoassay: Catalog# 05094798160 - Product Usage: intended to aid in the diagnosis of myocardial infarction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1636-2021·2021-05-26

    Biopsybell Easynject Device Recalled for Potential Sterility Failure

    Biopsybell is recalling five Easynject vertebroplasty devices because they were labeled sterile but may not have been sterilized.

    Product
    EASYNJECT, Device for cement infusion in the vertebroplasty procedure, REF KVTGUN-DS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0551-2021·2021-05-26

    Udi Gluten Free Banana Chocolate Chip Muffins Recalled for Plastic

    Conagra Brands is recalling Udi Gluten Free Banana Chocolate Chip Muffins due to the potential presence of plastic.

    Product
    Udi Gluten Free Banana Chocolate Chip Muffins, 10oz retail container of 4 muffins, 6 retail units per wholesale case. Retail unit UPC: 00-6-98997-81012-4
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1647-2021·2021-05-26

    Biopsybell 10G Direct Working Cannula Recalled for Sterilization Concerns

    Biopsybell is recalling 10G Direct Working Cannulas labeled as sterile because they may not have been sterilized. The recall affects 50 units distributed in Mississippi and Kentucky.

    Product
    10G DIRECT WORKING CANNULA BEVEL TIP 15CM, CODE INTVM-DWCB/15
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1594-2021·2021-05-26

    WillowWood Alpha Interlock Suspension System Lanyard Body Recalled for Pin Defect

    WillowWood Global LLC is recalling 815 Alpha Interlock Suspension System Lanyard Bodies because a shorter dowel pin was used, which may cause the suspension cord to slip or come loose.

    Product
    Alpha Interlock Suspension System Lanyard Body: An external prosthetic device. The Alpha Lanyard includes suction with a one-way air expulsion valve plus a locking mechanism. Product design features an easy release mechanism. Available with or without a titanium pyramid. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0552-2021·2021-05-26

    Udi Gluten Free Chocolate Zucchini Muffins Recalled for Plastic Contamination

    Conagra Brands is recalling Udi Gluten Free Chocolate Zucchini Muffins due to the potential presence of plastic. Consumers should stop eating the product.

    Product
    Udi Gluten Free Chocolate Zucchini Muffins, 10oz retail container of 4 muffins, 6 retail units per wholesale case. Retail unit UPC: 00-6-98997-81014-8
    Category
    Food
    Distribution
    Distributed nationwide