Hill-Rom Manufacturing, Inc. CLINITRON CII Air Fluidized Therapy unit. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
CLINITRON CII Air Fluidized Therapy unit.
Brand
Hill-Rom Manufacturing, Inc.
Lot Codes / Batch Numbers
Model CII, Serial #CC(all numeric codes).
Products Sold
Model CII, Serial #CC(all numeric codes).
Hill-Rom Manufacturing, Inc. is recalling CLINITRON CII Air Fluidized Therapy unit. due to Malfunction of side-rail latching pin coupled with inadequate directions for use.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Malfunction of side-rail latching pin coupled with inadequate directions for use.
Recommended Action
Per FDA guidance
Consignees were notified by letter sent via Airborne express, on May 5, 2003. Side-rail latching pins will be replaced with a more robust version. Label indicating directions for use will be modified to include detailed information on proper procedures for moving the units.
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