Recall Z-2246-2020— Hill-Rom, Inc.
Class II · Terminated
Class II FDA medical device recall by Hill-Rom, Inc., initiated 2020-04-30, terminated 2024-01-23. FDA's recall record names no specific 510(k) clearance for this event. Product: Centrella Smart+ Bed, Catalog Number P7900. Reason: The Bed Exit System may fail to send a remote alert through the nurse call system if a remote alert was previously sent and cancelled at the in-room nurse call wall unit..
- Recalling firm
- Hill-Rom, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2020-04-30
- Terminated
- 2024-01-23
- Firm location
- Batesville, IN, United States
Product description
Centrella Smart+ Bed, Catalog Number P7900
Reason for recall
The Bed Exit System may fail to send a remote alert through the nurse call system if a remote alert was previously sent and cancelled at the in-room nurse call wall unit.
Data sourced from openFDA. This site is unofficial and independent of the FDA.