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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices

Hillrom Centrella Smart+ Hospital Beds Recalled for Nurse Call Issue

Agency Publication Date: October 25, 2024
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Summary

Baxter Healthcare Corporation is recalling approximately 2,967 Hillrom Centrella Smart+ Medical-Surgical Hospital Beds equipped with software version 1.27.000. These beds may experience a software interface issue when integrated with the Rauland Responder 5 Nurse Call System. While the bed's local exit alarm will sound at the bedside, the system may fail to transmit a remote alert to the nursing station, potentially delaying a response from medical staff when a patient attempts to exit the bed. No injuries or incidents have been reported to date.

Risk

The failure to transmit remote alerts through the nurse call system means healthcare staff may not be notified when a patient at high risk of falling attempts to leave their bed. This delay in response increases the risk of serious patient falls and related injuries.

What You Should Do

  1. This recall affects Hillrom Centrella Smart+ Medical-Surgical Hospital Beds equipped with software version 1.27.000.
  2. Identify if your equipment is affected by checking the product codes on the bed label. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled device. Contact the manufacturer, Baxter Healthcare Corporation, or your authorized distributor to arrange for a software update or correction.
  4. For additional questions or technical support, call the FDA at 1-888-463-6332 (1-888-INFO-FDA).

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer Correction/Repair

How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Hillrom Centrella Smart+ Medical-Surgical Hospital Bed
Model / REF (57):
P7900B000001
P7900B100010
P7900B100024
P7900B100208
P7900B100273
P7900B100304
P7900B000005
P7900B100011
P7900B100025
P7900B100212
P7900B100277
P7900B100307
P7900B000010
P7900B100017
P7900B100026
P7900B100222
P7900B100281
P7900B1SPL05
P7900B000011
P7900B100018
P7900B100028
P7900B100223
P7900B100287
P7900B1SPL06
P7900B000020
P7900B100019
P7900B100039
P7900B100224
P7900B100288
P7900B000022
P7900B100020
P7900B100090
P7900B100231
P7900B100292
P7900B100001
P7900B100021
P7900B100161
P7900B100237
P7900B100293
P7900B100005
P7900B100022
P7900B100203
P7900B100242
P7900B100294
P7900B100009
P7900B100023
P7900B100205
P7900B100264
P7900B100296
P7900A000001
Serial Numbers:
All serial numbers with software version 1.27.000
UDI:
00887761985162
00887761999961

Software version 1.27.000. Recalled due to an interface issue with the Rauland Responder 5 Nurse Call System.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95402
Status: Active
Manufacturer: Baxter Healthcare Corporation
Sold By: Government distribution; Military distribution; Direct sales
Manufactured In: United States
Units Affected: 2,967 beds
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.