FDA Device recall Z-0361-2014
Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US)
- FDA Device
- Class II
- terminated
- Published 2013-11-27
On 2013-11-27 the FDA classified a Class II recall of Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US) by Aesculap, citing the trial insertion instrument may disassemble during use due to a potentially weak weld on then trial inserter shaft block area located near the thumb wheel.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0361-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-09-20 |
| Published | 2013-11-27 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Aesculap |
| Distribution | US |
Product
Aesculap Arcadius XP L Trial Insertion Instrument (ME020R/ME020R-US)
Reason
The trial insertion instrument may disassemble during use due to a potentially weak weld on then trial inserter shaft block area located near the thumb wheel.
Identifiers
| code_info | model no. ME020R |
|---|
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-0361-2014%22
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