Drugs & medicalClass II

Full Vision Inc recalls FULL VISION INC. TRACKMASTER, TREADMILL TMX428CP 220V, Model #317-07929

This has been identified a rare occurrence, under a specific scenario, where the circuit is found in a latch-up condition on the PCB that controls the safety function of the Magnetic Safety Tether, that when the magnet…

Read the official notice →
Date
2022-12-14
Country
United States
Brand
Full Vision
Product
FULL VISION INC. TRACKMASTER, TREADMILL TMX428CP 220V, Model #317-07929
Classification
Class II
Units
Wi, GA, NY, Mexico
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Full Vision recalls

  1. 2023-07-12
  2. US
    Drugs & medicalClass II

    Full Vision Inc recalls TRACKMASTER, TREADMILL GE T2100-ST2 220V CHINA, MODEL NUMBER 317-07927GE CHINA

    Treadmill malfunction: drive PCB can misread the signals and stop or reverse and then accelerate forward.

    FDA · DeviceFull Vision IncUSA (Nationwide), Australia, Bahrain, Canada, Chile, Colombia, Costa Rica,…Official notice →
All 2 Full Vision recalls →

Other drugs & medical recalls in the United States

  1. 2022-12-14
  2. US
    Drugs & medicalClass II

    Carefusion 2200 Inc recalls Carefusion V. Mueller" CUSHING BAYONET BIPOLAR FORCEPS, 2.0MM TIP, INSULATED OVERALL LENGTH 7-1/2" (190MM), REF F-2004

    BD has determined that the Instructions For Use (IFU) provided by BD is missing certain content that is contained in the manufacturer's IFU. This missing content is related to the interface with the device power…

    FDA · DeviceCarefusion 2200 IncNationwide, Austria, Canada, Egypt, Germany, Hong Kong, Israel, Philippines,…Official notice →
  3. US
    Drugs & medicalClass II

    Medacta Usa Inc recalls NextAR Shoulder Surgical Technique, Shoulder NextAR RSA Platform, CT based computer-assisted surgical navigation platform used to perform…

    A warning has been added to the Surgical Technique for NextAR Shoulder, advising verification of suitable patient conditions prior to placement of the NextAR Shoulder Target Holder: WARNING Target fixation requires…

    FDA · DeviceMedacta Usa IncAL, FL, NH, CO, IL, SC, AROfficial notice →
  4. US
    Drugs & medicalClass II

    Bunnell, Inc. recalls 2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025; and 2.5 mm LifePort Endotracheal Tube Adaptors inside Patient Circuit…

    Some adaptors, for use with high frequency ventilators, were packaged improperly, and may deform at the tip, which may impair the ability to pass a suction catheter or may affect normal ventilator performance, which…

    FDA · DeviceBunnell, Inc.US Nationwide Distribution: PA, NY, AR, AZ, TN, SC, MA, FL, CA, TX, MD, VA,…Official notice →
  5. US
    Drugs & medicalClass II

    Randox Laboratories Ltd. recalls IgM Immunoturbidimetric Assay-In vitro determination of IgA and IgM in serum and plasma Catalog Number: IM3834

    Update to the carryover avoidance technical bulletin to detail that IgA and IgM assays should not be run immediately after Fructosamine Catalogue Number FR3133 or FR4030 on the RX instruments testing order. Can lead to…

    FDA · DeviceRandox Laboratories Ltd.US Nationwide Distribution: CA, NC, NJ and WV,Official notice →
  6. US
    Drugs & medicalClass II

    Cardinal Health recalls Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 ml) 5ml Catheter Product Code: 2480 Intended for urinary drainage from the…

    Occlusion (blockage) of the bubble inlet port of the urinary drainage bag which may prevent urine draining into the bag. If the bladder is not emptied within a clinically appropriate time, this may increase the risk of…

    FDA · DeviceCardinal HealthNationwideOfficial notice →
  7. US
    Drugs & medicalClass II

    Siemens Healthcare Diagnostics, Inc. recalls IMMULITE and IMMULITE 1000 Total Testosterone Assay- In vitro diagnostic use with the IMMULITE and IMMULITE 1000 Analyzers…

    Confirmed an average positive bias of 40% for testosterone concentrations of approximately 660 ng/dL (22.9 nmol/L) and above with the IMMULITE/IMMULITE 1000 Total Testosterone Assay when compared to the IMMULITE…

    FDA · DeviceSiemens Healthcare Diagnostics, Inc.Worldwide Distribution: US (nationwide) to states of: AL, CA, FL, GA, IN, KY,…Official notice →
See all drugs & medical recalls →