News Release

Proprietary medical device repair harms hospitals, could threaten patients, during COVID-19 pandemic

New report finds that medical device manufacturers have denied critical resources to nearly half of surveyed medical repair professionals since March
For Immediate Release

The coronavirus (COVID-19) pandemic is putting incredible stress on the U.S. medical system, including the equipment that is essential to diagnose and treat patients, such as ventilators. As that equipment is pressed into round-the-clock use, biomedical repair technicians face increasing pressure to maintain and repair all that equipment. However, in too many cases, manufacturers limit access to the essential tools and information these repair experts need. A new report by the OSPIRG Foundation, Hospital Repair Restrictions, details the challenges that medical professionals face as a result of device manufacturers setting up barriers to repair, and outlines steps to take to help hospitals. 

The report includes a survey of 222 medical repair professionals, as well as dozens of interviews. Among the most troubling findings is how common restricted repair is -- with 91.8 percent of respondents reporting that they have been denied access to service information for “critical equipment (defibrillators, ventilators, anesthesia machines, imaging equipment, etc.).” 

“There is a strong financial incentive for manufacturers to restrict repair. They want to get hospitals to buy repair service contracts from the manufacturer,” said Nathan Proctor, OSPIRG Foundation's Right to Repair Campaign Director and one of the authors of the report. “Manufacturers typically charge much more for repairs than if the hospitals hire a third party or train their own technicians -- but more costs aren’t the only price of proprietary repair. Delays in getting equipment running put patients at risk.” 

Since March, OSPIRG Foundation has called for manufacturers of medical devices, especially ventilators, to cooperate with biomedical technicians and provide the information, parts, and other service information needed to repair critical medical equipment. In April, a number of manufacturers responded to public outcry by releasing additional service information for ventilators. 

Of the 153 survey respondents whose departments work with ventilators, 29.2 percent report that they currently (as of June 12, 2020) have ventilators that they cannot use because they lack access to parts and service information. 

"Restricted access to service materials for critical health care equipment has become a growing problem that hospitals are dealing with everyday. COVID-19 has been a kind of stress test for our medical system – and unnecessary manufacturer-imposed restrictions on repair is a barrier to safe and effective care, but one of the easiest to remedy," said Sam Jacques, VP of Clinical Engineering at McLaren Health Care. 

Manufacturers claim that these restrictions are in place to ensure patient safety. However, the Food and Drug Administration (FDA), in a 2018 study, found that third-party repair carries no additional risk and, just like manufacturers, “provide high quality, safe, and effective servicing of medical devices.”

“We need to stand up and help our hospitals right now. One easy thing we can do is to remove barriers to fixing life-saving medical equipment. It’s no time to be proprietary,” added Proctor. 

A copy of the report to download is available here.

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