DeviceSignal · Recall classified
Pride Mobility Products Corp.
FDA classified a device recall on 2026-07-31 · Class II · Z-2852-2026
EventRecall classified
Effective2026-07-31
ClassificationClass II
On 2026-07-31 the FDA classified a device recall from Pride Mobility Products Corp. as Class II. Product: Brand Name: Quantum Rehab Product Name: 4Front Model/Catalog Number: 4Front Software…. Recall Z-2852-2026. The firm initiated it on 2026-06-25. This reports the classification FDA published on that date.
Reported facts
- Recall number
- Z-2852-2026
- Classification
- Class II
- Classified on
- 2026-07-31
- Initiated on
- 2026-06-25
- Firm
- Pride Mobility Products Corp.
- Reason
- If the "Remind Me Later" option is selected for user reminders, reminder pop-up messages may appear while the wheelchair is in use. If this occurs while driving the wheelchair, the wheelchair may perform an unexpected park brake stop, which may result in fall or injury. If this occurs while not driving the wheelchair, the control system may crash and remain in pre-operational mode.
- Product
- Brand Name: Quantum Rehab Product Name: 4Front Model/Catalog Number: 4Front Software Version: 2.0.11, new version: 2.0.13 Product Description: Wheelchair, Powered (ITI), 890.3860 Component: Controller
Every field above is as fda_device_enforcement published it. Nothing on this page is our interpretation.
Provenance
- Source
- fda_device_enforcement
- Source record
Z-2852-2026- Snapshot hash
ab5ada73bf212eb52a548aab0968a0fcee42807c61b0350e60e24bb6e2beed72- Source URL
- https://download.open.fda.gov/device/enforcement/device-enforcement-0001-of-0001.json.zip
- Observed
- 2026-09-08T16:22:09.483Z
- Transform
fda_device_enforcement_to_recall v1- Event rule
fda_device_recall_classified v1- Event key
cd1cd81d3b374aef2e095dfa8e9f8ab72064b39a0556e712239aec702fd4327f- Signal type
device_recall.classified
Source terms that apply
- This is not a public alerting service and must not be used to notify patients or the public
- We do not report whether a recall is still open; FDA does not maintain that after classification
- Nothing here is a medical or clinical decision aid
- Not affiliated with, endorsed by, or certified by the FDA
Data provided by the U.S. Food and Drug Administration (https://open.fda.gov)