Medical Industries America Inc RemRest Non-Invasive Continuous Positive Airway Pressure System, Model 903. The firm name on the device is Medical Industries America Inc., Adel, IA. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
RemRest Non-Invasive Continuous Positive Airway Pressure System, Model 903. The firm name on the device is Medical Industries America Inc., Adel, IA.
Brand
Medical Industries America Inc
Lot Codes / Batch Numbers
All serial numbers beginning with C0424
Products Sold
All serial numbers beginning with C0424
Medical Industries America Inc is recalling RemRest Non-Invasive Continuous Positive Airway Pressure System, Model 903. The firm name on the de due to Units could show an error code and stop functioning.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Units could show an error code and stop functioning.
Recommended Action
Per FDA guidance
The recall was initiated via telephone on 9/3/04 to their customers explaining the reason for recall and instructing them to hold the units for further instruction. A telephone call to the customers on 9/10/04 instructed them to return the units for correction and replacement and to notify the end users.
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
CO, FL, IL, IN, IA, LA, MA, MO, NY, NC, TX, WV
Page updated: Jan 10, 2026