Centrella Smart+ Bed — Class II medical device recall Z-2246-2020
Terminated recall by Hill-Rom, Inc., reported 2020-06-10, distributed nationwide. The Bed Exit System may fail to send a remote alert through the nurse call system if a remote alert was previo
| Recall number | Z-2246-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hill-Rom, Inc., Batesville, IN, United States |
| Recall initiated | 2020-04-30 |
| Classified | 2020-06-02 |
| Reported by FDA | 2020-06-10 |
| Terminated | 2024-01-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA |
| Quantity | 4,381 beds |
| Reason classes | device malfunction |
| Model numbers | P7900 |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2246-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.