Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 109–120 of 581 recalls
Complaints of the ceramic tip of the resection sheath breaking have been received.
Complaints of the ceramic tip of the resection sheath breaking have been received.
Complaints of the ceramic tip of the resection sheath breaking have been received.
Product being removed due to incompatibility when used in conjunction with a GreenLight Laser for BPH therapy which could damage the tip of the device.
Products were mislabeled as the 6mm product but included the 5 mm product.
Firm is initiating a removal due to continued reports of adverse events.
Firm is initiating a removal due to continued reports of adverse events.
Firm is initiating a removal due to continued reports of adverse events.
Firm is initiating a removal due to continued reports of adverse events.
Firm is initiating a removal due to continued reports of adverse events.
Firm is initiating a removal due to continued reports of adverse events.
Firm is initiating a removal due to continued reports of adverse events.