CareFusion - Alaris 8100
by CareFusion

The Alaris® Pump module is designed for the delivery of fluids, medications, blood and blood products using continuous or intermittent delivery for adult, pediatric or neonatal patients. Infusion delivery can occur via clinically acceptable routes of administration (e.g., intravenous, intra-arterial, subcutaneous, epidural, enteral or irrigation of fluid spaces).
2Replies3 months ago | Error 242.4030 I have replaced all of the recommended items listed in this forum for the error, and I am still getting Error 242.4030. // Any ideas???? or please call me at 713-873-4305 Equipment: Alaris (BD) 8100 Module Reply |
4Repliesa year ago | service manual service manual Equipment: CareFusion - Alaris 8100 Reply |
4Repliesa year ago | error code What is error code 211.2000? Equipment: CareFusion - Alaris 8100 Reply |
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death.