Cardinal Health 303 Inc DBA Alaris Products Pyxis Anesthesia System 3500, Cardinal Health, Clinical Technologies and Services, San Diego, CA Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Pyxis Anesthesia System 3500, Cardinal Health, Clinical Technologies and Services, San Diego, CA
Brand
Cardinal Health 303 Inc DBA Alaris Products
Lot Codes / Batch Numbers
All serial numbers of the Pyxis Anesthesia Station, Model 3500
Products Sold
All serial numbers of the Pyxis Anesthesia Station, Model 3500
Cardinal Health 303 Inc DBA Alaris Products is recalling Pyxis Anesthesia System 3500, Cardinal Health, Clinical Technologies and Services, San Diego, CA due to System lock up; mini-drawers -under certain circumstances during use, are not accessable, delaying the user from accessing critical medications.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
System lock up; mini-drawers -under certain circumstances during use, are not accessable, delaying the user from accessing critical medications.
Recommended Action
Per FDA guidance
The field action consisted of phone calls and a mailing conducted to all customers for the Pyxis Anesthesia System 3500 beginning on 08/13/2007. The customers will be notified by registered return receipt mail by Recall Notifications dated August 14, 2007. Separate letters will be sent to the Director of Pharmacy, Chief of Anesthesia, Director of Risk Management, and Director of Surgery at each facility. Recommended actions will be provided as a short-term fix and a long-term fix of the software will be issued shortly.
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