LifeShield Infusion Safety Software Suite – LifeShield CDR
LifeShield Clinical Dashboards & Reports is the reporting component of the LifeShield Infusion Safety Software Suite. It displays infusion and device information received from compatible…
LifeShield Clinical Dashboards & Reports is the reporting component of the LifeShield Infusion Safety Software Suite. It displays infusion and device information received from compatible Plum Duo pumps through LifeShield Data Flow Management.
Clinical administrators can view ongoing infusion status, pump asset information and operational status. Dashboards summarize infusion or asset metrics, while an analytics viewer provides historical data. Information can cover one or several facilities within the customer account.
Listed Item
Infusion Safety Management Software
Data and Clinical Roles
The cloud-based suite manages connected pump data for trained healthcare professionals. CDR supports review, trending and quality-improvement analysis; its information does not generate patient treatment decisions or pathways. The suite also contains separate drug-library and device-management services. Infusion-parameter entry and validation remain with the trained healthcare professional.
Who Else Makes It
Registered in Shanghai. One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Jabil Circuit (Shanghai) Ltd. | Shanghai | Shanghai | Contract manufacturer | 31 |
Record
| Listed by | ICU Medical, Inc, United States |
|---|---|
| FDA product code | PHC |
| Device type | Infusion Safety Management Software |
| Device class | Class 2 |
| Regulation | 21 CFR 880.5725 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer |
| 510(k) | K223606 |
| Record published | 2023-10-03 |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Prescription | Prescription only |
| Label carries | lot or batch number |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 2.1 | In distribution | |
| 2.1 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Ivenix Infusion System | Fresenius Kabi AB | 6 |
| BD Intelliport | Becton, Dickinson AND Company | 5 |
| PharmGuard | ICU Medical, Inc | 4 |
| LifeShield Infusion Safety Software Suite | ICU Medical, Inc | 3 |
| Dose IQ Safety Software | Baxter Healthcare Corporation | 3 |
| Alaris | CareFusion 303, Inc | 3 |
| ICU Medical MedNet | ICU Medical, Inc | 3 |
| Alaris™ Guardrails™ Editor Software Kit, Model 8961 | CareFusion 303, Inc | 2 |
| BD Alaris | CareFusion 303, Inc | 1 |
| BD Alaris™ System Manager 9601, Software | CareFusion 303, Inc | 1 |
| Vigilant Software Suite | Fresenius Kabi AB | 1 |
| BD Intelliport System | Becton, Dickinson AND Company | 1 |
Showing 12 of 20. All products under Infusion Safety Management Software
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K252130 | 2026-04-02 |
| K242117 | 2025-04-02 |
| K223606 | 2023-08-24 |
Recalls Naming This Product
1 recall names this product by its own identifier, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|---|---|
| ICU Medical, Inc | 510(k) number | 2025-05-02 | Class II | Software Design Change | Firm has identified Drug Library Management defects in the software: 1) DLM software does not allow user to create percentage dose rate or rate change values with certain limits, potentially resulting in over-delivery to patient. 2) An unau | 12 US, 3 OUS |
Recalls
2 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|
| 2025-11-24 | Class II | Software Design Change | Software issue only allows Concentration Limits to be defined to one digit of precision past the decimal point (0.1) instead of three digits (0.001). If the user is unable to use Concentration Limits as intended, they may need to change the | 12 customers |
| 2025-11-24 | Class II | Software Design Change | For certain customers, the Change Summary review option ceases to operate as expected for any migrated library after the migration has been completed. Users must use alternate methods to review changes. Failure to do so may lead in over del | 7 customers |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.