Philips Healthcare Inc. IntelliVue Clinical Information Portfolio (ICIP) Critical Care Release D, Version D.02. Intended for use in data collection, storage, and management with independent bedside devices, and ancillary systems that are connected either directly or through networks. It is indicated for use by healthcare providers whenever there is a need for generation of a patient record and computation of drug dosage. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
IntelliVue Clinical Information Portfolio (ICIP) Critical Care Release D, Version D.02. Intended for use in data collection, storage, and management with independent bedside devices, and ancillary systems that are connected either directly or through networks. It is indicated for use by healthcare providers whenever there is a need for generation of a patient record and computation of drug dosage.
Brand
Philips Healthcare Inc.
Lot Codes / Batch Numbers
S/W Version D.02
Products Sold
S/W Version D.02
Philips Healthcare Inc. is recalling IntelliVue Clinical Information Portfolio (ICIP) Critical Care Release D, Version D.02. Intended fo due to A software defect exists in the ICIP Release 0.02 scheduling function for order management such that if a user edits either the Schedule Time or the S. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
A software defect exists in the ICIP Release 0.02 scheduling function for order management such that if a user edits either the Schedule Time or the Stop Time for an existing order, the corresponding intervention(s) for the order may not be created.
Recommended Action
Per FDA guidance
Philips Medical Systems notified accounts by letter on October 21, 2009, of the release ICIP version D.03, which contains a software correction . A Philips representative will schedule the implementation of this upgrade. Please contact the Philips Customer Care Center with questions or concerns about this correction at 1-800-722-9377.
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 noticeDistribution
As reported by FDA
MD, RI, TX, WV
Page updated: Jan 10, 2026