The Recall Desk

State

Maine product recalls

20,364 recalls have nationwide distribution and so reach Maine. 0 additional recalls listed Maine specifically in their distribution scope.

About recalls in Maine

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Maine consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

14326–14350 of 20364

  • HighFDA (Devices)·Z-1040-2023·2023-02-08

    Siemens Fluoroscopic X-ray Systems Risk of Boot Failure After Shutdown

    Certain Siemens fluoroscopic X-ray systems may only boot into backup mode after an abrupt shutdown, preventing full operation. This could necessitate cancelling or switching to alternative treatment systems.

    Product
    System Material # Artis zee floor 10094135 Artis zee ceiling 10094137 Artis zee multi-purpose 10094139 Artis zee biplane 10094141 Artis zeego 10280959 Artis Q floor 10848280 Artis Q ceiling 10848281 Artis Q biplane 10848282 Artis Q.zeego 10848283 Artis Q.zen floor 108
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1027-2023·2023-02-08

    Temperature Monitoring Adapter Detachment in Cardiopulmonary Bypass Oxygenators

    Medtronic is recalling cardiopulmonary bypass equipment because the Temperature Monitoring Adapter can come loose during setup or disassembly, potentially compromising temperature monitoring during heart surgery.

    Product
    Custom Pack Perfusion Tubing Packs containing Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, REF BB811. Used in Cardiopulmonary bypass.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1025-2023·2023-02-08

    Cardiopulmonary Bypass Oxygenator Recalled for Loose Temperature Monitoring Adapter

    Medtronic Perfusion Systems is recalling 1,340 units of the Affinity Fusion Oxygenator due to reports that the Temperature Monitoring Adapter can come loose during or after use in cardiopulmonary bypass procedures.

    Product
    Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, Custom Packs, REF CB811. Used in Cardiopulmonary bypass.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1035-2023·2023-02-08

    Non-sterile procedural knee trays recalled for potential packaging breach

    Medline Industries recalls non-sterile Total Knee procedural trays because sterile blades inside can puncture the outer foil packaging. This could compromise sterile blade integrity.

    Product
    Non-sterile procedural trays labeled as TOTAL KNEE KIT, 1 per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1033-2023·2023-02-08

    Non-sterile orthopedic procedural trays recalled for potential sterile packaging breach

    Medline Industries recalls non-sterile orthopedic procedural trays that may contain sterile blades capable of puncturing the protective foil packaging, compromising sterile barriers.

    Product
    Non-sterile procedural trays labeled as ORTHO TRAUMA, 1 per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1032-2023·2023-02-08

    Non-sterile procedural trays with potential sterile packaging breach

    Medline Industries is recalling non-sterile procedural trays containing sterile blades that may damage sterile packaging due to blade puncture risk. Lot 22IBQ980. No illnesses reported.

    Product
    Non-sterile procedural trays labeled as MAJOR/MINOR, 3 per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1029-2023·2023-02-08

    MEDLINE procedural trays recalled for potential sterile packaging breach

    MEDLINE is recalling procedural trays because sterile blades within the kits could puncture the outer foil packaging, potentially breaching the sterile barrier.

    Product
    Non-sterile procedural trays labeled as CRANI, 2 per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1030-2023·2023-02-08

    Non-sterile procedural trays risk sterile packaging breach

    Medline Industries is recalling non-sterile laparoscopic procedural trays containing sterile blades that may puncture the outer packaging, potentially breaching the sterile barrier. 260 cases have been distributed nationwide.

    Product
    Non-sterile procedural trays labeled as LAPAROSCOPIC, 2 per case
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1045-2023·2023-02-08

    MEDLINE UNITE Foot and Ankle Screw Recall: Intra-Operative Failure

    MEDLINE INDUSTRIES is recalling 420 units of UNITE Foot and Ankle surgical screws (Lot 810304) due to observed intra-operative failure when pre-drilled and implanted with excessive torque.

    Product
    MEDLINE UNITE FOOT & ANKLE Screw, Non-Locking, Mini T8 (2.0x8mm), REF MMSN2008
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V664000·2023-02-08

    2021 Dodge Challenger Safety System Status Indicators May Not Illuminate Properly

    2021 Dodge Challenger vehicles may not properly illuminate safety system status indicators in daylight or nighttime conditions. This could prevent drivers from knowing the status of vehicle safety systems, increasing crash risk.

    Product
    DODGE — 2021 DODGE CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1023-2023·2023-02-08

    Medtronic Affinity Fusion Oxygenator: Temperature Monitoring Adapter May Detach

    Medtronic is recalling 2,937 Affinity Fusion Oxygenators used in cardiac surgery because the Temperature Monitoring Adapter may detach during setup or disassembly.

    Product
    Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, Custom Packs, REF BB811. Used in Cardiopulmonary bypass.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1026-2023·2023-02-08

    Affinity Fusion Oxygenator adapter may loosen during cardiac surgery

    Medtronic is recalling Affinity Fusion Oxygenators because the Temperature Monitoring Adapter may come loose during setup or disassembly of the heart-lung machine used in cardiac surgery. No injuries have been reported.

    Product
    Affinity Fusion Oxygenator with Integrated Arterial Filter and Balance Biosurface, Custom Packs, REF CB841. Used in Cardiopulmonary bypass.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0323-2023·2023-02-08

    Vitamin B Complex dietary supplement recalled due to undeclared niacin

    Professional Complementary Health Formulas, LLC recalls Vitamin B Complex dietary supplement (lot 1092715) due to undeclared niacin affecting 299 bottles distributed nationwide.

    Product
    Vitamin B Complex packaged in white plastic bottle labeled in part, "***PROFESSIONAL FORMULAS COMPLEMENTARY HEALTH Vitamin B Complex DIETARY SUPPLEMENT 60 Capsules***Supplement Facts Serving Size: One Capsule***Vitamin B1 (as thiamine Hcl) 80mg 6667% Vitamin B2 (as riboflavin) 80
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1050-2023·2023-02-08

    Ultrasound system hard drive defect causes device freezing and failure

    FDA recall of NovaGuide Intelligent Ultrasound System due to faulty hard drive causing device freezing and eventual system failure.

    Product
    NovaGuide Intelligent Ultrasound System, Model: NA-RBTSYS1. Comprised of NovaBot Automated Headset (AKA: NeuralBot, Model: NA-RBT1) and Lucid TCD 2.0 Transcranial Doppler Ultrasound (Model: NA-LUCM1)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0322-2023·2023-02-08

    Inositol dietary supplement recalled due to undeclared niacin

    Professional Complementary Health Formulas is recalling Inositol dietary supplement (Lot 1032526, UPC 4065111562) distributed in NY, OR, PA, UT, WI, and WY due to undeclared niacin. Consumers should stop using the product.

    Product
    Inositol packaged in white plastic bottle with UPC 4065111562 and labeled in part, "***PROFESSIONAL FORMULAS COMPLEMENTARY HEALTH Inositol DIETARY SUPPLEMENT 360 Capsules***Supplement Facts Serving Size: One Capsule***Inositol 920 mg***Other Ingredients: Vegetarian capsule (hypro
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1041-2023·2023-02-08

    Biopsy marker device recalled for label and contents mismatch

    Carbon Medical Technologies recalls 550 Mammotome MammoStar biopsy markers due to a labeling error. The label identifies one product but the package contains a different marker size and shape.

    Product
    Mammotome MammoStar Biopsy Site Identified, REF STAR1401
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1049-2023·2023-02-08

    Lucid TCD 2.0 Transcranial Ultrasound System Recalled for Hard Drive Failure

    The Lucid TCD 2.0 System has a faulty hard drive that causes the device to freeze and reboot. Eventually, the system becomes completely inoperable.

    Product
    Lucid TCD 2.0 System, Model: NA-LUCM1. Transcranial Ultrasound System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V566000·2023-02-07

    2021–2022 Spartan K2 RV Chassis Fuel Leak Recall

    Shyft Group is recalling certain 2021–2022 Spartan K2 RV Chassis vehicles with Cummins L9 Diesel Engines due to fuel leaks from pressurized hoses. The leak may increase fire risk if an ignition source is present.

    Product
    SPARTAN — 2021 SPARTAN K2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V569000·2023-02-07

    2021 Audi E-Tron recalled for brake booster defect

    Volkswagen is recalling certain 2021 Audi E-Tron models due to improperly welded brake boosters that may separate, reducing braking assistance and stability control.

    Product
    AUDI — 2021 AUDI E-TRON
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V397000·2023-02-06

    Commercial Buses and Trucks Recalled for Brake Pressure Switch Fire Risk

    Navistar is recalling certain IC BUS and International commercial buses and trucks due to a brake pressure switch defect that may cause electrical short and fire risk. Owners should park vehicles outside until repairs are completed.

    Product
    IC BUS — 2022 IC BUS CE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V400000·2023-02-06

    Commercial trucks: park brake warning light may illuminate incorrectly

    Autocar commercial trucks from 2016-2023 may have a faulty pressure switch causing the park brake warning light to malfunction, increasing crash risk. Dealers will replace the pressure switch at no cost.

    Product
    AUTOCAR — 2016 AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V398000·2023-02-06

    IC Bus CESB school buses recalled for brake pressure switch fire risk

    Navistar is recalling certain IC Bus CESB school buses with brake pressure switch assemblies that may leak brake fluid and cause electrical short-circuits, creating a fire risk while driving or parked.

    Product
    IC BUS — 2023 IC BUS CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V396000·2023-02-05

    2022 Thor Motor Coach RV models recalled for solar panel fire risk

    Thor Motor Coach is recalling certain 2022 Sequence, Rize, Scope, and Tellaro recreational vehicles. The Flex-190 solar panel junction box may experience electrical shorts, increasing the fire risk.

    Product
    THOR MOTOR COACH — 2022 THOR MOTOR COACH SEQUENCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V391000·2023-02-05

    Heavy-duty trucks recalled for fuel rail defect and fire risk

    PACCAR is recalling certain 2018-2021 Kenworth and Peterbilt commercial trucks because a sealing washer defect in the fuel rail assembly may cause fuel leaks. When fuel leaks occur near an ignition source, fire risk increases.

    Product
    KENWORTH — 2021 KENWORTH T880
    Category
    Vehicle
    Distribution
    Distributed nationwide