Z-0625-2019Class II

Covidien Emprint Long Percutaneous Antenna with Thermosphere Technology, Material CA30L2 intended for use in...

Name: Z-0625-2019 Covidien Emprint Long Percutaneous Antenna with Thermosphere Technology, Material CA30L2 intended for use in...
Creator: Covidien LLC
Published: 2018-11-15
License: https://open.fda.gov/license/

Medtronic, Inc. / initiated 2018-11-15 / Open, Classified / root cause: manufacturing process

FDA source

Covidien LLC began a recall of Covidien Emprint Long Percutaneous Antenna with Thermosphere Technology, Material CA30L2 intended for use in percutaneous, laparoscopic, and intraoperative... on 2018-11-15. FDA classified it as Class II and gives the reason as "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". As of 2026-09-10, the recall status on record is Open, Classified, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-0625-2019
Classification: Class II
Status: Open, Classified
Initiated: 2018-11-15
Posted: 2018-12-18
Recalling firm: Medtronic, Inc.
Product: Covidien Emprint Long Percutaneous Antenna with Thermosphere Technology, Material CA30L2 intended for use in percutaneous, laparoscopic, and intraoperative coagulation (ablation) of soft tissue, including partial or complete ablation of nonresectable liver tumors.
Product code: NEY System, Ablation, Microwave And Accessories
Reason for recall: 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.
Root cause tag: manufacturing process
FDA root cause: Nonconforming Material/Component
Action: On November 15, 2018 Medtronic issued UPDATED URGENT MEDICAL DEVICE RECALL notices to customers. Customers are advised to take the following actions: 1. Please immediately quarantine and discontinue use of the affected products. 2. Return affected product as indicated. 3. If you have distributed the products, please promptly forward the information from the letter to those recipients. 4. Complete the Recalled Product Return Form even if you do not have inventory. If you have any questions or concerns, please do not hesitate to contact your Medtronic representative or Technical Support at (800) 448-3644, Option 3, Option 8.
Distribution: US Nationwide
Product codes and lots: GTIN Number - 10884521706606 Lot Numbers- S7HG007KX S7HG008KX S7HG009KX S7HG032LX S7HG033LX S7HG034LX S7JG008LX S7JG009X S7JG012X S7KG012LX S7KG038QX S7LG009X S7MG010LX S7MG019X S8BG004X S8BG005X S8CG002X S8DG001X S8DG026X S8EG004X

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0625-2019
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0625-2019	Class II	Ongoing	Voluntary: Firm initiated	2018-12-26	2018-12-18
Z-0626-2019	Class II	Ongoing	Voluntary: Firm initiated	2018-12-26	2018-12-18
Z-0627-2019	Class II	Ongoing	Voluntary: Firm initiated	2018-12-26	2018-12-18

Product code NEY

K163105Class IIEmprint Ablation SystemCovidien, LLC / cleared 2016-12-06

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-10-07, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)