Sunrise Medical (US) LLC Quickie/Zippie powered wheelchair. Q700M wheelchair. A battery operated powered wheelchair, which is controlled by Power Module RNET 120A Expandable (Item No.: 250ER10, Part No.: 123966). Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Quickie/Zippie powered wheelchair. Q700M wheelchair. A battery operated powered wheelchair, which is controlled by Power Module RNET 120A Expandable (Item No.: 250ER10, Part No.: 123966).
Brand
Sunrise Medical (US) LLC
Lot Codes / Batch Numbers
Part No.: 123966). Controller label: D50903.15 CR19100531.
Products Sold
Q700M wheelchair S/N Q7MP-083941. UDI:(01)05022408059799. Power Module RNET 120A Expandable (Item No.: 250ER10, Part No.: 123966). Controller label: D50903.15 CR19100531.
Sunrise Medical (US) LLC is recalling Quickie/Zippie powered wheelchair. Q700M wheelchair. A battery operated powered wheelchair, which is due to Due to programming errors in the Controller, an increase in the set motor parameters can be made by the end user beyond tested safe limits.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Due to programming errors in the Controller, an increase in the set motor parameters can be made by the end user beyond tested safe limits.
Recommended Action
Per FDA guidance
An URGENT: MEDICAL DEVICE RECALL letter was sent the firm's dealer. The dealer was instructed on February 4, 2020, to replace the controller unit for the device.
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
IN, MT
Page updated: Jan 10, 2026