None of the items were made by Amazon, but they were available via its website until the retailer became aware of the recalls. Amazon subsequently contacted its affected customers and publicized the ...

The company began the recall after receiving four field complaints about tip separation before and during use.

The FDA issued a notice identifying a high-risk device issue associated with a Medtronic recall of Bravo CF capsule delivery ...

The FDA is amplifying a recall from Medtronic for its acid reflux testing system, after the company said it received 33 ...

The FDA announced a recall of certain Medtronic Bravo esophageal pH monitoring capsules, which help in diagnosing ...

The Food and Drug Administration published an early alert for the recall on Tuesday. No deaths have been associated with the ...

The U.S. Food and Drug Administration (FDA) has announced an expansion of an earlier Medtronic recall, now issuing a new Class 1 recall for Medline Industries' procedure kits that contain Medtronic ...

In a comment made Tuesday, CMS chief Mehmet Oz pushed for the elimination of the payments drugmakers send to pharmacy benefit managers after prescriptions are filled. Other industry news is about a ...

According to a new listing at the FDA device recalls and alerts webpage, Dublin-based Medtronic plc., requested customers quarantine any Bravo CF capsules, an esophageal pH monitoring system.

Relating to certain of Medtronic’s Newport ventilator range, users have been advised to remove the affected units from circulation.

Medtronic Embolization Devices: The recall impacts the Pipeline Vantage devices compatible only with 0.027" inner diameter microcatheters, Medtronic said. The company added that it has taken the ...