Reported Jun 10, 2020 · Terminated

Centrella Smart+ Bed, Catalog Number P7900

Hill-Rom, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Hill-Rom, Inc. · 1069 State Road 46 E · Batesville, IN · 47006-7520

Is this the product you have?

  • Centrella Smart+ Bed, Catalog Number P7900
Lot codes and dates
  • Serial codes anufactured between U290PF8145 through V015PF2473 plus the following serial codes outside this range
  • that were updated during servicing

    2,469 of 2,469 codes

    • S237PF0789
    • T222PF6473
    • U067PF5719
    • U079PF6209
    • S248PF1062
    • T223PF6496
    • U067PF5722
    • U079PF6210
    • S249PF1117
    • T223PF6497
    • U067PF5725
    • U079PF6211
    • S254PF1218
    • T227PF6698
    • U071PF5783
    • U079PF6212
    • S255PF1262
    • T236PF7213
    • U071PF5788
    • U079PF6213
    • S256PF1300
    • T241PF7583
    • U071PF5789
    • U079PF6214
    • S257PF1353
    • T249PF8023
    • U071PF5790
    • U079PF6215
    • S300PF2244
    • T250PF8146
    • U072PF5798
    • U079PF6216
    • S303PF2287
    • T268PF9463
    • U078PF6163
    • U079PF6217
    • S303PF2306
    • T268PF9468
    • U078PF6166
    • U079PF6247
    • S305PF2366
    • T277PF9896
    • U078PF6169
    • U079PF6248
    • S331PF2510
    • T277PF9926
    • U078PF6171
    • U079PF6249
    • S332PF2554
    • T281PF0056
    • U078PF6173
    • U079PF6250
    • S333PF2570
    • T282PF0110
    • U078PF6174
    • U079PF6251
    • S339PF2673
    • T282PF0113
    • U078PF6175
    • U079PF6252
Amount recalled
4381 beds

Where it was sold

  • Nationwide

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.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jan 23, 2024 · Data as of Sep 19, 6:16 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.