The chief executive at Abbott Laboratories said Wednesday he's not ready to predict if recent action by federal regulators at the company's St. Jude Medical business in Little Canada will slow approval for a key product.
St. Jude Medical has been losing share in the market for implantable cardiac defibrillators (ICD) because its heart devices have lacked technology to make them compatible with MRI scans.
A warning letter this month from the U.S. Food and Drug Administration (FDA) called for changes at St. Jude's manufacturing facility for defibrillators, and analysts have speculated the action could delay approval for St. Jude's "MRI-safe" ICD. Company officials have projected the clearance will come during the second half of 2017.
The MRI feature has boosted sales for rivals Medtronic and Boston Scientific, which have large operations in the Twin Cities.
"At this point, I'm not going to change our launch dates or our assumptions on approval dates and so forth, because I don't see a reason to do that, yet, or a direction to do it in," Chief Executive Miles White said during a conference call Wednesday with investors.
"We've had a pretty good head start here on the issues," White said. "We've been aware of the circumstances here for some time."
Wednesday marked the first release of quarterly results for Abbott since it closed in January on a $25 billion acquisition of St. Jude Medical.
"The integration of St. Jude is going well and recently launched products are contributing to double-digit sales growth across several areas of our medical devices business," White said in a statement.