FDA Device recall Z-2823-2020
Alaris Syringe Module Model 8110 - Product Usage: is intended to provide trained healthcare caregivers a way to automate the programming of…
- FDA Device
- Class II
- ongoing
- Published 2020-08-26
On 2020-08-26 the FDA classified a Class II recall of Alaris Syringe Module Model 8110 - Product Usage: is intended to provide trained healthcare caregivers a way to automate the programming of… by Carefusion 303, citing LED display, which provides infusion or patient monitoring values, on the module may have segments that appear dim.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2823-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2020-06-30 |
| Published | 2020-08-26 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Carefusion 303 |
| Distribution | US |
Product
Alaris Syringe Module Model 8110 - Product Usage: is intended to provide trained healthcare caregivers a way to automate the programming of infusion parameters, thereby decreasing the amount of manual steps necessary to enter infusion data.
Reason
LED display, which provides infusion or patient monitoring values, on the module may have segments that appear dim.
Identifiers
| code_info | All serial numbers |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2823-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.