Hill-Rom, Inc.: Medical Device Recalls in 2020

Updated on March 25, 2026.

According to to data from the FDA, there were 3 medical device recalls made by Hill-Rom, Inc. in 2020. See the details of the recalls below.

You can see similar recalls for other firms.

Data Source: FDA.

See this for other years:

Centrella Smart+ Bed, Catalog Number P7900
Centrella Smart+ Bed, Catalog No. P7900 - Product Usage: intended to be used to treat or prevent pulmonary or other complications associated with immobility; to treat or prevent pressure ulcers; or for any other use where medical benefits may be derived from either Continuous Lateral Rotation Therapy or Percussion/Vibration Therapy.
Progressa Bed, Catalog No. P7500 - Product Usage: intended to be used to treat or prevent pulmonary or other complications associated with immobility; to treat or prevent pressure ulcers; or for any other use where medical benefits may be derived from either Continuous Lateral Rotation Therapy or Percussion/Vibration Therapy.