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MEDICAL DEVICE RECALLMODERATE

Quantum 4Front 2 Wheelchair Controller

Quantum Rehab recalls the Quantum 4Front 2 wheelchair controller over a software issue that can cause unexpected park brake stops.

What to do

Contact Pride Mobility Products Corp. to obtain the software update (version 2.0.13) for your Quantum 4Front 2 wheelchair. Do not select the "Remind Me Later" option for user reminders until the update is installed.

Recalled
Listed
Updated
Recall No.
Z-2841-2026
Agency
FDA
Firm
Pride Mobility Products Corp.
Recall ID
99286
Status
ONGOING

Why it was recalled

Quantum Rehab is recalling the Quantum 4Front 2 powered wheelchair due to a software issue in the controller. If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use, potentially causing an unexpected park brake stop while driving, which may result in fall or injury. The control system may also crash and remain in pre-operational mode when not driving.

Is mine affected?

This recall covers 13 products. Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

Software version: 2.0.11, new version: 2.0.13

ProductLot codeRecall #UDI-DI
Quantum Rehab Q6 Edge 3 Stretto41875Z-2843-20260060650920018
Quantum Rehab Quantum Outback41875Z-2842-20260060650920024
Quantum Rehab Quantum 4Front 24Front, 41875Z-2841-20260060650920019
Quantum Rehab 4Front4Front, 41875Z-2852-20260060650920003
Quantum Rehab Q6 Edge HD41875Z-2845-20260060650920005
Quantum Rehab Quantum 14501450, 41875Z-2847-20260060650920009
Quantum Rehab Quantum Rival41875Z-2853-20260060650920013
Quantum Rehab R-TRAK41875Z-2844-20260060650920022
Show all 13 products
ProductLot codeRecall #UDI-DI
Quantum Rehab Q6 Edge 341875Z-2849-20260060650920015
Quantum rehab Q6 Edge 2.02.0, 41875Z-2846-20260060650920004
Quantum Rehab Q6 Edge 2.0 (ilevel)2.0, 41875Z-2848-20260060650920004
Quantum Rehab Q6 Edge 441875Z-2850-20260060650920028
Quantum Rehab Quantum 4Front 2HD4Front, 2HD, 41875Z-2851-20260060650920020

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Official source

View on U.S. Food and Drug Administration →

Other Device Defect recalls

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Editorial summary by Recall Canary · summary updated 2026-09-03 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification