Invacare Corporation Pronto M51 Wheelchair, component- seat Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Pronto M51 Wheelchair, component- seat
Brand
Invacare Corporation
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
There is no code on the individual seat. Recall covers seats on wheelchairs distributed between 03/14/2006 and 04/07/2006.
Invacare Corporation is recalling Pronto M51 Wheelchair, component- seat due to Some of the wheelchairs were distributed with seats that did not have a seat positioning strap.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Some of the wheelchairs were distributed with seats that did not have a seat positioning strap.
Recommended Action
Per FDA guidance
The recalling firm sent a recall letter, dated 06/06 to 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 noticePage updated: Jan 10, 2026