FDA Device recall Z-2018-2014
Terumo¿ Advanced Perfusion System 1 100/120V AC, Advanced Perfusion System Platform (APS)
- FDA Device
- Class II
- terminated
- Published 2014-07-16
On 2014-07-16 the FDA classified a Class II recall of Terumo¿ Advanced Perfusion System 1 100/120V AC, Advanced Perfusion System Platform (APS) by Terumo Cardiovascular Systems, citing an evaluation of the APS1 Operator Manual found that existing instructions lack clarity and accuracy related to specific items.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2018-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-06-17 |
| Published | 2014-07-16 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Terumo Cardiovascular Systems |
| Distribution | US |
Product
Terumo¿ Advanced Perfusion System 1 100/120V AC, Advanced Perfusion System Platform (APS)
Reason
An evaluation of the APS1 Operator Manual found that existing instructions lack clarity and accuracy related to specific items.
Identifiers
| code_info | Catalog Number 801763 |
|---|
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-2018-2014%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.