FDA Device recall Z-0560-2018
Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 30cm, Material CA30L1
- FDA Device
- Class II
- ongoing
- Published 2018-02-14
On 2018-02-14 the FDA classified a Class II recall of Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 30cm, Material CA30L1 by Covidien, citing the firm received consumer reports of the ceramic trocar tip of the Emprint ablation antenna disengaging from the needle shaft post-ablation. This can result in the tip remaining….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0560-2018 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2017-08-07 |
| Published | 2018-02-14 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Covidien |
| Distribution | US |
Product
Covidien Emprint Percutaneous Antenna with Thermosphere Technology, 30cm, Material CA30L1
Reason
The firm received consumer reports of the ceramic trocar tip of the Emprint ablation antenna disengaging from the needle shaft post-ablation. This can result in the tip remaining in the patient.
Identifiers
| code_info | UDI 10884521189553, Lot codes: S5LG004PX,S6AG001X,S6BG002X,S6BG005X,S6BG016PX,S6CG003X,S6CG005X,S6CG017X,S6DG004X,S6EG0…UDI 10884521189553, Lot codes: S5LG004PX,S6AG001X,S6BG002X,S6BG005X,S6BG016PX,S6CG003X,S6CG005X,S6CG017X,S6DG004X,S6EG001X,S6FG001X,S6FG006X,S6FG010X,S6KG002X,S6KG006PRX,S6KG006PX,S6LG004X,S6MG002X,S7CG001PCX,S7CG011PCX,S7CG015CX,S7EG001X,S7EG003X,S7FG011PX |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0560-2018%22
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