FDA Classifies Q'Apel Medical's Recall of Aspiration System as Class I
"Glad to see Q'Apel prioritizing patient safety!"
"What exactly led to the Warning Letter from the FDA?"
"It's concerning that such a serious recall is necessary."
"I wonder how this will impact Q'Apel's future innovations."
"The risks associated with aspiration catheters are alarming!"
"Could they have handled the regulatory issues differently?"
"Can't wait to see what new technology they develop next!"
"This makes me wary of using similar devices in the future."
"What kind of support will be available for affected patients?"
"Seems like a big step back for a company known for innovation."
2025-04-18T19:03:00.000Z
Hans Schneider
Source of the news: www.prnewswire.com