Hill-Rom Manufacturing, Inc. Clinitron At Home Air Fluidized Therapy Bed Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Clinitron At Home Air Fluidized Therapy Bed
Brand
Hill-Rom Manufacturing, Inc.
Lot Codes / Batch Numbers
Serial numbers: CS102304, CS103257, CS103901, CS103902, CS103903, CS103904, CS103909, CS103911, CS103914, CS103915, CS103916, CS103917, CS103919, CS103921, CS103923, CS103924, CS103925, CS103928, CS103932, CS103933.
Products Sold
Serial numbers: CS102304, CS103257, CS103901, CS103902, CS103903, CS103904, CS103909, CS103911, CS103914, CS103915, CS103916, CS103917, CS103919, CS103921, CS103923, CS103924, CS103925, CS103928, CS103932, CS103933.
Hill-Rom Manufacturing, Inc. is recalling Clinitron At Home Air Fluidized Therapy Bed due to Sudden unexpected lowering of the head of the bed may occur due to failure of the had of the bed actuator.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Sudden unexpected lowering of the head of the bed may occur due to failure of the had of the bed actuator.
Recommended Action
Per FDA guidance
Customer letter was hand delivered to consignees by Hill-Rom Service Technicians 05/20/2005. The affected product will be corrected by replacement of the actuator with one from an unaffected lot.
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, FL, KY, LA, MA, NY, NC, TN, TX, VA
Page updated: Jan 10, 2026