Reported Aug 12, 2026 · Ongoing
Brand Name: Quantum Rehab Product Name: Quantum 1450 Model/Catalog Number: Quantum 1450 Software Version: 2.0.11, new…
Pride Mobility Products Corp.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Pride Mobility Products Corp. · 401 York Ave · Duryea, PA · 18642-2025
Is this the product you have?
- Brand NameQuantum
- Rehab Product NameQuantum 1450
- Model/Catalog NumberQuantum 1450
- Software Version2.0.11
- new version2.0.13
- Product DescriptionWheelchair, Powered (ITI), 890.3860
- ComponentController
- Lot codes and dates
- Lot CodeQuantum 1450 0060650920009*7 K112815 D143578 41875 ITI
- Amount recalled
- 1102
This recall covers 13 products
The agency filed one notice per product. You are reading one of them; the other 12 are below.
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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