Centrella Smart+ Bed
Medical device recall Z-2246-2020. Published in FDA’s Enforcement Report on Jun 10, 2020.
No Watch here, and no alerts: openFDA asks that its enforcement data “should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall” (openFDA). For FDA’s own recall emails, subscribe at FDA. FDA’s own record is on accessdata.fda.gov.
The short answer
Published in FDA’s Enforcement Report on Jun 10, 2020. Copied from openFDA on Oct 20, 2026.
- Class II FDA’s class
- Terminated its status, in FDA’s file
- Nationwide FDA’s word for where it went
- 4381 beds how much, in FDA’s words
Every line below is in FDA’s own words, with its source beside it. FDA’s terms are explained in FDA’s own words.
How serious is it, by FDA’s class?
Class II, the middle of FDA’s three classes.
“Products that might cause a temporary health problem, or pose only a slight threat of a serious nature. Example: a drug that is under-strength but that is not used to treat life-threatening situations.”
openFDA, in plain words, its enforcement report fields.
“Class II is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.”
FDA’s rule, 21 CFR 7.3(m)(2), eCFR.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
What’s wrong with it?
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.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Which ones are recalled?
Centrella Smart+ Bed, Catalog Number P7900
4381 beds, in FDA’s words.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Codes to check against yours
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…
Every code shown here, 1,998 characters
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 U079PF6256 S354PF3029 T303PF0798 U078PF6180 U079PF6257 T002PF3078 T324PF1681 U078PF6181 U079PF6258 T003PF3090 T333PF2061 U078PF6182 U079PF6259 T003PF3099 T340PF2401 U078PF6183 U079PF6260 T003PF3101 T347PF2679 U078PF6184 U079PF6263 T003PF3102 T348PF2725 U078PF6185 U079PF6264 T003PF3111 T353PF2876 U078PF6186 U079PF6266 T003PF3113 T353PF2896 U078PF6187 U079PF6267 T004PF3119 U023PF3849 U078PF6188 U079PF6268 T004PF3153 U025PF4032 U078PF6189 U079PF6269 T009PF3187 U029PF4099 U078PF6190 U079PF6270 T078PF4163 U032PF4222 U078PF6191 U079PF6271 T079PF4173 U036PF4335 U078PF6192 U079PF6272 T079PF4177 U036PF4366 U078PF6193 U079PF6273 T079PF4182 U038PF4450 U078PF6194 U079PF6274 T079PF4185 U042PF4523 U078PF6195 U079PF6275 T079PF4187 U043PF4568 U078PF6196 U079PF6276 T099PF4537 U043PF4606 U079PF6197 U079PF6277 T102PF4616 U043PF4618 U079PF6198 U080PF6278 T103PF4638 U045PF4631 U079PF6199 U080PF6279 T106PF4657 U045PF4648 U079PF6200 U080PF6282 T135PF5209 U045PF4668 U079PF6201 U080PF6283 T138PF5276 U046PF4726 U079PF6203 U080PF6284…
FDA’s list runs to 27,308 characters. The first part is shown; the rest is on FDA’s record.
Copied exactly as FDA lists them: lot and serial numbers, dates and other codes on the product or its label.
Where did it go?
FDA’s words for the “general area of initial distribution”: where the firm first shipped it.
Domestic distribution nationwide. Foreign distribution to Canada and Australia.
These words name no state.
What FDA means by nationwide
“The term “nationwide” is defined to mean the fifty states or a significant portion. Note that subsequent distribution by the consignees to other parties may not be included.”
openFDA, its enforcement report fields.
The words say it went outside the United States too.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
Is it still going on?
Terminated, in FDA’s file.
“FDA has determined that all reasonable efforts have been made to remove or correct the violative product in accordance with the recall strategy, and proper disposition has been made according to the degree of hazard.”
openFDA, on “Terminated”, its enforcement report fields.
What these words mean is quoted from openFDA’s field reference and 21 CFR 7.3.
- The firm began the recall on Apr 30, 2020.
- FDA classified it on Jun 2, 2020.
- FDA’s Enforcement Report published it on Jun 10, 2020.
- FDA terminated it on Jan 23, 2024.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
Who is recalling it?
- Hill-Rom, Inc., of Batesville, IN.
- Who began it, in FDA’s words: Voluntary: Firm initiated.
- How the firm first told its customers: Letter.
FDA, Device recall enforcement reports. Released Oct 14, 2026. Updated weekly.
What this record can’t tell you
- Whether your own one is affected: compare the codes, dates and numbers above with yours. When unsure, ask the firm or the store.
- Where it went after the firm’s first shipments. FDA’s words cover the firm’s initial distribution, and, in FDA’s words, “subsequent distribution by the consignees to other parties may not be included.”
- How many have been returned, corrected or destroyed: FDA’s report doesn’t say.
- Whether anyone was hurt or fell ill: the report doesn’t say.
- How current it is: openFDA publishes FDA’s Enforcement Report weekly, after FDA does, and a firm can announce a recall weeks before it appears there. openFDA’s own caution: “This data should not be used as a method to collect data to issue alerts to the public, nor should it be used to track the lifecycle of a recall.”
- FDA’s list of codes runs to 27,308 characters; the first part is shown here, and the rest is on FDA’s record.
- A product with no recall here isn’t safe by that: FDA’s report lists the recalls FDA classified, and when.
Hearth Record wrote these lines; the quotations are FDA’s.
Sources
-
U.S. Food and Drug Administration, Device recall enforcement reports.
Released Oct 14, 2026 and checked Oct 20, 2026. Updated weekly. Public domain (CC0 1.0, openFDA). FDA asks that nothing suggest it endorses this site.
Recalls of food, medicines, medical devices, pet food and animal drugs are from the U.S. Food and Drug Administration (FDA). FDA does not endorse Hearth Record. openFDA: “Do not rely on openFDA to make decisions regarding medical care.” Copied on Oct 20, 2026.