The story about Boston Scientific pacemakers isn’t just about a failed battery; it is a story about a company that was aware of the battery defect yet it chose to do nothing, and the only reason why the public caught wind of the same was because of some courageous journalists that chose to file Freedom of Information Act requests forcing the company to part with documents it never intended to reveal in the first place. The FOIA paper trail started when former employees that were privy to some things started seeing things inside the Arden Hills campus which worried them senseless, and what the journalists that received these tips uncovered would eventually reveal a pattern of negligent corporate behavior which went far beyond a simple manufacturing error. The documents reveal information about how test failures were ignored, warnings that were never heeded and quality control systems that were never adequate. If you received a recall notice regarding your Boston Scientific Accolade pacemaker and are wondering how a company could be so careless with your life and what your legal options are for justice and compensation, then you’ve come to the right place – read on to find out more about this conundrum and what to personally do next.
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What the FOIA Documents Actually Revealed
Here’s an overview of what was gleaned from the secret Boston Scientific pacemaker documents:
- The documents showed that dozens of test batteries failed between 2019 and 2023, but the company never issued a warning to neither physicians nor patients, and they instead continued selling and marketing the devices while at the same time investigating the matter internally
- FOIA disclosure also showed that Boston Scientific didn’t analyze battery test data from 2013 to 2021, which created a snowball effect whereby by the time the problem was discovered, years of vital data wasn’t available which could have alerted them to the defect earlier.
- Inspection reports also revealed that Boston Scientific’s quality control systems were never sufficient when it came to detecting the cathode defect before device implantation, and no basic testing protocols were implemented for years.
- The documents also revealed that the company’s internal reporting protocols were designed to minimize the visibility of battery failures, and test results which may have led to immediate action being buried in reports that were never sent over to senior management
Why The FOIA Paper Trail is Pivotal to Your Pacemaker Lawsuit
This FOIA paper trail is damning evidence when it comes to product liability lawsuits since it established that the company was aware of the defect, yet failed to act. This evidence may be used when it comes to filing claims under punitive damages and also rebut any defense argument that the company acted in a reasonable manner with regard to handling the recall.
Best Boston Scientific Accolade Pacemaker Lawyers – Call Us Today!
If you were fitted with a Boston Scientific Accolade pacemaker and are looking to file a claim to recover compensation for the economic and non-economic damages you endured, please give us a call wherever you are in the country at (314) 481-63338 for your 100% FREE consultation into all things pacemaker failure recall lawsuits. Thanks for choosing McCready Law, and we look forward to helping you.