Cardiology Devices Recalled Due to Serious Injury and Death
A Class I recall has been issued for two defective devices: cardiac guidewire devices. The Rotawire Elite and wireClip Torquer, manufactured by Boston Scientific, have been pulled from the market after being linked to serious complications, including death. TLF: The Medical Injury Law Firm is currently accepting clients who have been injured, or who have lost loved ones as a result of these defective devices. The Rotablator Rotational Atherectomy System