Olympus Corporation Of The Americas recalls Olympus Thunderbeat 5 mm
Firm is initiating a removal due to continued reports of adverse events.
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 601–612 of 674 recalls
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.
Potential packaging failures, which could lead to a breach in the sterile barrier.
Potential packaging failures, which could lead to a breach in the sterile barrier.
Potential packaging failures, which could lead to a breach in the sterile barrier.
Due to product that may contain a void in the material that separates the wire guide and cutting wire lumens, which may cause an inappropriate path of current during cutting.
The mix up of the impression caps provided in the package. The provided impression caps are magenta instead of brown.
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reac…
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reac…
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reac…
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reac…