FDA Device recall Z-2372-2015
Alaris Medley LVP Bezel Assembly
- FDA Device
- Class I
- terminated
- Published 2015-08-26
On 2015-08-26 the FDA classified a Class I recall of Alaris Medley LVP Bezel Assembly by Elite Biomedical Solutions, citing administration of inappropriate quantities of fluid can result, with the potential to cause injury or death.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2372-2015 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2015-06-03 |
| Published | 2015-08-26 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Elite Biomedical Solutions |
| Distribution | US |
Product
Alaris Medley LVP Bezel Assembly. Intended use to hold platen assembly and help protect the bezel assembly's internal components from fluid intrusion. This part is used in the Alaris Medley LVP 8100 infusion pump.
Reason
Administration of inappropriate quantities of fluid can result, with the potential to cause injury or death.
Identifiers
| code_info | P/N 49000204 Lot #'s 031815100, 032415100, 04061545 and 043015215 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2372-2015%22
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