Mexico’s Health Care Agency Alleges Zimmer Fraud

Mexico’s health care agency is suing Zimmer Biomet for a refund on purchases it made from the company during a long-running bribery scheme. The agency claims the bribery, which was admitted in a 2017 settlement with the US government, nullified its contracts with the device maker.

Mexico
• Source: Shutterstock

Zimmer Biomet Holdings Inc. should refund Mexico’s government for more than $2.6m in illicit profits, the Instituto Mexicano del Seguro Social (Mexican Institute of Social Security, or IMSS) alleged in a lawsuit filed on 30 January in an Indiana federal court. IMSS, which provides health care services in Mexico, is suing to recoup what it spent on products made by Zimmer Biomet and its predecessor, Biomet Inc., during what the agency says was a widespread and long-running bribery scheme. Zimmer merged with Biomet in 2015. (Also see "Zimmer, Biomet Sell Off Some U.S. Assets As They Finalize A $14 Bil. Merger" - Medtech Insight, 25 June, 2015.)

The companies have settled charges that they violated overseas bribery laws with the US Securities and Exchange Commission and Department of Justice in the recent past. In 2012, Biomet paid $22.8m to resolve allegations of bribery in Argentina, Brazil and China. And in 2017, the now-merged companies paid $30.5m and entered into a deferred prosecution agreement after confessing bribery in Mexico and Brazil

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Medtech Insight for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Latin America

More from Geography

FDA Announces Classifications On 8 Device Types

 
• By 

The US Food and Drug Administration has announced new classifications for eight device types that reached market via the de novo process, with most of the newly classified products in the diagnostics sector.

Medical Devices Not The Focus Of FDA’s Plans To Step Up Foreign Inspections, Expert Says

 

The US FDA recently announced plans to carry out more unannounced inspections of foreign facilities. But those inspections will primarily target drug producers, with less attention and resources allocated to those making devices.

State And International Enforcement Agencies May Step Up Amid Uncertain Federal Environment

 
• By 

States and international regulatory bodies may increase their US enforcement role following federal staff cuts, Hyman Phelps & McNamara attorneys said in a recent webinar. The attorneys also expect False Claims Act enforcement and public health to remain key areas of focus at the federal level.