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…

Read the official notice →
Date
2023-07-05
Country
United States
Brand
Permobil
Product
PushTracker E2 component utilized with the SmartDrive MX2+ Power Assist Device (Part Numbers: MX2-32K, MX2-32P, MX2-32PK, MX2-33D,…
Classification
Class II
Units
Worldwide distribution.
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 Details may be shortened or out of date; the official notice is the authoritative source.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. US
    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…

    FDA · DevicePermobil IncWorldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO,…Official notice →
All 3 Permobil recalls →

Other drugs & medical recalls in the United States

  1. 2023-07-05
  2. US
    Drugs & medicalClass II

    Limacorporate S.p.A recalls REF 1975.14.800, Prima TT Genoid Modular Reverse TT Baseplate, Sterile R

    Due to manufacturing issue, their is a potential for peripheral holes to be out of specification.

    FDA · DeviceLimacorporate S.p.AUS Nationwide distribution in the states of MI, IL, ND, MO, OK.Official notice →
  3. US
    Drugs & medicalClass II

    Covidien, LLC recalls Medtronic ILLUMISITE Platform Console, Model Number ILS-1000-CS

    Single ILLUMISITE Platform Console was converted from a 220-240VAC model to a 120VAC configuration using a non-supplied power cord and non-supplied fuses in the field by Medtronic Field Service Engineer.

    FDA · DeviceCovidien, LLCInternational distribution in the country of Taiwan.Official notice →
  4. US
    Drugs & medicalClass II

    Baxter Healthcare Corporation recalls NaviCare Patient Safety V3.9.200 to 3.9.600, used with the Centrella Bed

    Baxter identified a potential risk where the "safety" monitoring and "bed exit" monitoring features may enter a permanent state of alert suppression. In this state, a caregiver may not be alerted remotely when assigned…

    FDA · DeviceBaxter Healthcare CorporationUS Nationwide distribution in the states of OR, SC, VA, TN, GA, NC, CO, NC, FL.Official notice →
  5. US
    Drugs & medicalClass II

    B. Braun Medical, Inc. recalls Design Options¿ / Epidural anesthesia kit (10 count carton)

    Kits were assembled with the incorrect Filter Straw.

    FDA · DeviceB. Braun Medical, Inc.US Nationwide distribution.Official notice →
  6. US
    Drugs & medicalClass I

    Megadyne Medical Products, Inc. recalls MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode. used during electrosurgery

    Firm has received reports of patient burns in surgical procedures where device was used.

    FDA · DeviceMegadyne Medical Products, Inc.Distributed US Nationwide.Official notice →
  7. US
    Drugs & medicalClass II

    Ellex Medical Pty Ltd. recalls Integre Pro Yellow LP561, Integre Pro Yellow LP6RY, Integre Pro Scan Green LP6G, Integre Pro Green LP5532 Spare, Optics Bench V2, L2G/LP6G

    When using a Laser-Indirect-Ophthalmoscope (LIO) as the delivery device, a scattered laser beam inside the laser cavity system may unintentionally exit through the Slit Lamp output port (SDS) and get emitted from the…

    FDA · DeviceEllex Medical Pty Ltd.US nationwide/ Worldwide DistributionOfficial notice →
See all drugs & medical recalls →