Medical device recalls Moderate risk

Hill-Rom, Inc. recalls Centrella Smart+ Bed, Catalog Number P7900

Recall date
April 30, 2020
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2246-2020
FDA classification
Class II
Brand / firm
Hill-Rom, Inc.
Sold / distributed
Domestic distribution nationwide. Foreign distribution to Canada and Australia.

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Centrella Smart+ Bed, Catalog Number P7900

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