FDANovember 15, 2018device

Covidien Emprint Standard Percutaneous Antenna with Thermosphere Technology, CA20L2 intended for use in percutaneous, laparoscopic, and intraoperative coagulation (ablation) of soft tissue, including partial or complete ablation of nonresectable liver tumors.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Ongoing

Brands named

covidien

UPCs

10884521706590

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Covidien Emprint Standard Percutaneous Antenna with Thermosphere Technology, CA20L2 intended for use in percutaneous, laparoscopic, and intraoperative coagulation (ablation) of soft tissue, including partial or complete ablation of nonresectable liver tumors. — Recall Details · AllClear