Frank Mobility Systems, Inc. e-fix E19 power drive. The product is a wheelchair component/accessory. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
e-fix E19 power drive. The product is a wheelchair component/accessory.
Brand
Frank Mobility Systems, Inc.
Lot Codes / Batch Numbers
Model number E19
Products Sold
Model number E19
Frank Mobility Systems, Inc. is recalling e-fix E19 power drive. The product is a wheelchair component/accessory. due to may short circuit within the interface due to long term exposure of liquid. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
may short circuit within the interface due to long term exposure of liquid
Recommended Action
Per FDA guidance
The recalling firm issued a Corrective Action Notice to their customers on 9/1/04 via certified mail return receipt. The notice described the problem and the correction (interface was designed). The notice also instructed the dealers/distributors to notify their customers and have the units brought back to them for the exchange.
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