By: Danielle Kirsh
The FDA is advising healthcare providers not to use BioZorb Markers and BioZorb LP Markers made by Hologic following a recent recall.
Danielle Kirsh is a Senior Editor in the Life Sciences division at MassDevice, a leading source of medical device news. With a focus on the medtech industry, Danielle covers a wide range of topics including acquisitions, regulatory approvals, product launches, and industry developments. Her work has also been featured in publications such as The Robot Report, Drug Delivery Business News, and Medical Design & Outsourcing.
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United States (National)
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Danielle Kirsh's focus on the healthcare and pharmaceutical industry with a heavy emphasis on press releases and private sector announcements suggests she may be responsive to pitches that provide exclusive access to breaking news, insights into new products or acquisitions, or expert opinions from leaders within medical technology companies.
Given her frequent coverage of FDA approvals and medical device recalls, experts in regulatory affairs and product quality control would likely find success in reaching out to Danielle.
As there is no specified geographic focus for Danielle's articles, it appears she covers global developments within the healthcare and pharmaceutical industry. If you have expertise relevant to breaking news within this field or can offer valuable insights into trends affecting medtech companies globally, your pitch could resonate well with her coverage.
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