FDAApril 20, 2022device

Cardioblate" Gemini"-s Irrigated RF Surgical Ablation System; The device is placed in a plastic tray with a snap on plastic lid, the tray is placed in protective wrap, then into a sterile pouch, 1 device per carton, 1 carton per box.

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

The hazard

Firm detected an increase in complaints related to fractured jaw tips of the Cardioblate Gemini-s.

What to do

FDA enforcement status: Ongoing

Brands named

medtronic perfusion systemsmedtronicmedtronic perfusion

UPCs

00613994268051006139947556430064316998312000643169998117

Recall history

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

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Cardioblate" Gemini"-s Irrigated RF Surgical Ablation System; The device is placed in a plastic tray with a snap on plastic lid, the tray is placed in protective wrap, then into a sterile pouch, 1 device per carton, 1 carton per box. — Recall Details · AllClear