Hill-Rom Co., Inc. Integris Monitor Arm; model P997-04 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Integris Monitor Arm; model P997-04
Brand
Hill-Rom Co., Inc.
Lot Codes / Batch Numbers
All units manufactured prior to June 20, 2003.
Products Sold
All units manufactured prior to June 20, 2003.
Hill-Rom Co., Inc. is recalling Integris Monitor Arm; model P997-04 due to The monitor may separate from the monitor arm, allowing the monitor to fall from the arm.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The monitor may separate from the monitor arm, allowing the monitor to fall from the arm.
Recommended Action
Per FDA guidance
An Urgent Device Correction letter dated 8/8/03 was sent to each hospital account receiving these products. The recall was extended to two additional products via a second letter issued on August 25, 2003. Hospitals were asked to take the units out of service, if possible, until Hill-Rom can inspect/correct them.
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