Invacare Corporation Pronto Series Power Wheelchair, model M50. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Pronto Series Power Wheelchair, model M50.
Brand
Invacare Corporation
Lot Codes / Batch Numbers
All serial numbers between 05A000-05C999.
Products Sold
All serial numbers between 05A000-05C999.
Invacare Corporation is recalling Pronto Series Power Wheelchair, model M50. due to If the arm of the wheelchair is overloaded, the joystick mounting brackett and/or arm pivot may fail due to variability in the plastic used by the sup. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
If the arm of the wheelchair is overloaded, the joystick mounting brackett and/or arm pivot may fail due to variability in the plastic used by the supplier to make the components. This failure may cause the user or a caregiver to fall if they are leaning on the arm, and result in injury.
Recommended Action
Per FDA guidance
The recalling firm contacted all consignees by phone between May 9 and May 25, 2005 and sent an urgent field correction needed letter, dated April, 2005 to all consignees.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AZ, AR, CA, CO, FL, GA, IL, IN, IA, KS, KY, LA, ME, MD, MI, MN, MS, MO, MT, NV, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WV, WI
Page updated: Jan 10, 2026