United StatesThe M5 Corpus Power Wheelchair (REF 120032), UDI‑DI 17330818334562, with Power Platform firmware versions 1.27 through 1.57 is being recalled; 715 units were distributed worldwide including the United States and Canada. The Power Platform firmware is missing specific drive inhibit logic, which may allow the chair to drive under restricted conditions and may create an unstable condition in certain circumstances.
What's being recalled
M5 Corpus Power Wheelchair REF,120032
Recalling firm: Permobil Inc, Lebanon, TN, United States.
How to identify it
Power Platform firmware versions 1.27 through 1.57 UDI-DI 17330818334562
The hazard
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 certain circumstances.
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
Worldwide - US: Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KY, ME, MI, MN, MO, MS, MT, NC, ND, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI, WV, WY and the country of CANADA.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)