Hill-Rom, Inc. 125 E Pearl St 1069 State Route 46 East Batesville IN 47006 Hill-Rom TotalCare Bed, Model P1900. The TotalCare (R) Bed System is intended to provide a patient support ideally suited to be used in health care environments. The TotalCare (R) Bed System may be used in a variety of settings including, but not limited to, acute care, including critical care, step down/progressive care, medical/surgical, high acuity sub-acute care, post Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Hill-Rom TotalCare Bed, Model P1900. The TotalCare (R) Bed System is intended to provide a patient support ideally suited to be used in health care environments. The TotalCare (R) Bed System may be used in a variety of settings including, but not limited to, acute care, including critical care, step down/progressive care, medical/surgical, high acuity sub-acute care, post
Brand
Hill-Rom, Inc. 125 E Pearl St 1069 State Route 46 East Batesville IN 47006
Lot Codes / Batch Numbers
Serial numbers from J329AM1149 through J339AM1343.
Products Sold
Serial numbers from J329AM1149 through J339AM1343.
Hill-Rom, Inc. 125 E Pearl St 1069 State Route 46 East Batesville IN 47006 is recalling Hill-Rom TotalCare Bed, Model P1900. The TotalCare (R) Bed System is intended to provide a patient due to An e-ring may not have been installed during production, which could result in an inability to latch the siderail.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
An e-ring may not have been installed during production, which could result in an inability to latch the siderail.
Recommended Action
Per FDA guidance
Consignees were notified by an Urgent Medical Device Correction letter dated 3/9/09 and were instructed that a Hill-Rom technician will visit each consignee to inspect and to correct the beds, if necessary. The firm asks that consignees locate and test their beds to make sure the siderails are latching correctly; forward a copy of the letter to users that were loaned or purchased the device and notify Hill-Rom of their new locations or owners; and if affected beds were disposed of or are no longer in use, to inform the firm of their serial numbers. If there are questions customers should contact their Hill-Rom Technical Support for their geographic region.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026