The name may be new, but the challenges are familiar.
Little Canada-based cardiac device maker St. Jude Medical became a part of Abbott Laboratories in Illinois earlier this month. But in the first earnings call since the deal, Abbott Labs CEO Miles White had to repeatedly address concerns about St. Jude's continuing lack of pacemakers and implantable defibrillators that can be safely used with magnetic-resonance imaging (MRI) scanners.
"CRM (cardiac rhythm management) I think has continued to struggle," White said Wednesday. "I mean, we can see that in the sales and the [market] share and so forth. I expect that to be rectified imminently here, shortly."
In 2016, St. Jude lost U.S. market share in sales of pacemakers and defibrillators to competitors like Medtronic and Boston Scientific, which have MRI-compatible devices.
St. Jude's U.S. sales of the two types of devices declined 17 percent in the three months ended Oct. 1.
The earnings figures released by Abbott Wednesday did not explicitly spell out St. Jude's CRM-device sales during its last quarter.
Like St. Jude executives last year, White projected a quick turnaround of the situation once the Food and Drug Administration grants MRI compatibility.
Responding to analysts' questions, White indicated the FDA may grant approval for MRI pacemakers during the first quarter of 2017, and for MRI defibrillators in the second half of 2017.