FDA Device recall Z-1444-2014
Smiths Medical HOTLINE¿ Fluid Warming Set L-80
- FDA Device
- Class II
- terminated
- Published 2014-04-16
On 2014-04-16 the FDA classified a Class II recall of Smiths Medical HOTLINE¿ Fluid Warming Set L-80 by Smiths Medical Asd, citing injection port of the Set may leak blood/ IV fluids from the septum of the injection port or the septum may become dislodged.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1444-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-03-17 |
| Published | 2014-04-16 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Smiths Medical Asd |
| Distribution | US |
Product
Smiths Medical HOTLINE¿ Fluid Warming Set L-80. Product Usage: intended for the delivery of warmed blood and intravenous fluids at normothermic temperatures under gravity conditions
Reason
Injection port of the Set may leak blood/ IV fluids from the septum of the injection port or the septum may become dislodged
Identifiers
| code_info | 2513261 2531612 2540540 2545044 2588656 |
|---|
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-1444-2014%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.