FDA Device recall Z-2246-2020
Centrella Smart+ Bed, Catalog Number P7900
- FDA Device
- Class II
- terminated
- Published 2020-06-10
On 2020-06-10 the FDA classified a Class II recall of Centrella Smart+ Bed, Catalog Number P7900 by Hill Rom, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2246-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-04-30 |
| Published | 2020-06-10 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Hill Rom |
| Distribution | US |
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.
Identifiers
| code_info | Serial codes anufactured between U290PF8145 through V015PF2473 plus the following serial codes outside this range that…Serial codes anufactured between U290PF8145 through V015PF2473 plus the following serial codes outside this range that were updated during servicing: 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 S340PF2717 T285PF0294 U078PF6176 U079PF6253 S346PF2865 T288PF0375 U078PF6177 U079PF6254 S347PF2912 T295PF0413 U078PF6178 U079PF6255 S347PF2919 T297PF0600 U078PF6179 U079 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2246-2020%22
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