Drugs & medicalClass II

Permobil Inc recalls Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3

This recall has been reported retroactively. The power wheelchair firmware lacks a speed restriction to maintain stability when the seat lift exceeds 50 mm, which may cause the user to fall from the wheelchair or the…

Read the official notice →
Date
2026-08-05
Country
United States
Brand
Permobil
Product
Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3
Classification
Class II
Units
Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO,…
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 Details may be shortened or out of date; the official notice is the authoritative source.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 Permobil recalls

  1. 2026-08-05
  2. US
    Drugs & medicalClass II

    Permobil Inc recalls M5 Corpus Power Wheelchair REF,120032

    This recall is being reported retroactively. Power Platform firmware is missing specific drive inhibit logic. This issue may allow the chair to drive under restricted conditions, and may create an unstable condition in…

    FDA · DevicePermobil IncWorldwide - US: Nationwide distribution in the states of AL, AR, AZ, CA, CO,…Official notice →
  3. 2023-07-05
  4. US
    Drugs & medicalClass II

    Permobil recalls PushTracker E2 component utilized with the SmartDrive MX2+ Power Assist Device (Part Numbers: MX2-32K, MX2-32P, MX2-32PK, MX2-33D,…

    When multiple processes are running on the watch's Central Processing Unit (CPU), the application may fail unexpectedly. If this happens, the motor on the power assist device continues to run and the user may not be…

    FDA · DevicePermobilWorldwide distribution.Official notice →
All 3 Permobil recalls →

Other drugs & medical recalls in the United States

  1. 2026-08-05
  2. US
    Drugs & medicalClass II

    Permobil Inc recalls M5 Corpus Power Wheelchair REF,120032

    This recall is being reported retroactively. Power Platform firmware is missing specific drive inhibit logic. This issue may allow the chair to drive under restricted conditions, and may create an unstable condition in…

    FDA · DevicePermobil IncWorldwide - US: Nationwide distribution in the states of AL, AR, AZ, CA, CO,…Official notice →
  3. US
    Drugs & medicalClass II

    Argon Medical Devices, Inc recalls L-Cath Midline S/L Catheter 20ga (3F) 1mm x 20cm, REF: 384620

    Catheters, indicated for short/long-term peripheral access to central venous system for the administration of fluids, medications, nutrients; and sampling, may experience leaking and/or cracking at the hub, which may…

    FDA · DeviceArgon Medical Devices, IncUS: AR, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, MA, MD, MI, MN, MO, MS, NC,…Official notice →
  4. US
    Drugs & medicalClass II

    Windstone Medical Packaging, Inc. recalls AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT Pack, Pack Number AMS12206; 2) ENT Pack, Pack Number…

    The recall notice was initiated due to a Medicom Urgent Medical Device Recall. Medicom is recalling specific lots of Ritmed¿ Neurological Sponges Non-Sterile Models 55992C to 55998C due to potential for unexpected…

    FDA · DeviceWindstone Medical Packaging, Inc.US Nationwide distribution in the states of AZ, CA, CT, GA, IL, MA, MD, NY,…Official notice →
  5. US
    Drugs & medicalClass I

    Medical Action Industries, Inc. 306 recalls Pack Angiography NCMC 3/Cs BANNER, REF: NCAG62I, containing Medline Namic Angiographic Star Off Handle Manifolds

    Cardiovascular procedure kits contain manifolds, the subject of another recall, that may have particulate within the fluid path, which has the potential to be introduced into blood circulation and become lodged within…

    FDA · DeviceMedical Action Industries, Inc. 306US: AZ, COOfficial notice →
  6. US
    Drugs & medicalClass II

    Terex Utilities recalls Power Over Fiber Base Module

    Device not certified - no laser product report was filed with CDRH prior to distribution. Product label incorrectly states device is "Class IV", although Class 1 is appropriate for device. Improperly labeled - omitted…

    FDA · DeviceTerex UtilitiesU.S. Nationwide Distribution and International DistributionOfficial notice →
  7. US
    Drugs & medicalClass I

    ResMed Ltd. recalls Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory support for…

    Due to a Supercapacitor electrolyte leakage on Printed Circuit Board Assembly (PCBA) may damage the charger chip, causing fail-safe state and interruption of ventilation therapy.

    FDA · DeviceResMed Ltd.Worldwide - U.S. Nationwide distribution including in the states of AK, AL,…Official notice →
See all drugs & medical recalls →