Devices

Device Recall Cardioblate Gemini Surgical Ablation Device

Model / Serial
Lot Numbers: J243, J547, J548 and J656
Product Classification
General and Plastic Surgery Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide Distribution including states of FL, IL, IN, LA, MI, PA, TN, TX, UT, and WI
Product Description
Medtronic Cardioblate Gemini-s, model 49260. Surgical Ablation Device. Sterilized using Ethylene Oxide. Two, unique jaw curvatures are provided: a standard curve (model 49260) and extra curve (Model 49261). The device is intended for intermittent operation. Manufacturer: Medtronic, Inc. Minneapolis, MN 55432-5604.
Manufacturer
Medtronic Cardiac Surgery Technologies
1 Event
- Recall of Device Recall Cardioblate Gemini Surgical Ablation Device

Manufacturer

Medtronic Cardiac Surgery Technologies

Manufacturer Address
Medtronic Cardiac Surgery Technologies, 7601 Northland Dr N, Minneapolis MN 55428-1088
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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