Medical device recalls are a big deal. In the past few years, we’ve seen a wide variety of medical devices recalled due to safety concerns. Some of these include surgical mesh used in hernia repair, knee implants, and birth control products. These recent recalls affect millions of people, so you must know about them as soon as possible. Here’s everything you need to know about some recent medical device recalls from this year!
Unauthorized Covid-19 Test Kit
Innova Medical Group has recalled at least 77,339 of its COVID-19 antigen tests after the FDA discovered the company was selling the test without its approval and that it carries the risk of false-positive and false-negative results.
COVID-19 antigen tests were recalled by the manufacturer due to a risk of false results. If you have been prescribed this test. You must contact your doctor as soon as possible for advice and follow-up testing options if necessary. It has been discovered that some batches may be faulty or inaccurate, which could lead to an incorrect diagnosis.
Heart Pump Device
Medtronic has recalled a heart pump device after discovering it sometimes failed to start or restart, an issue that led to two patient deaths.
One of these is the heart pump device, which is faulty in certain situations where it can fail to start or restart properly while implanted. There’s a case of Philips lawsuit, so you can research about it and find out does Philips CPAP even work? This causes dangerous blood clots due to lack of movement, so if this applies to your specific case, always seek help from a doctor immediately.
Smiths Medical, a St. Paul, Minn.-based medical device maker, has recalled several lots of insulin syringes after discovering some had skewed measurement markings.
There have been several medical device recalls that you need to be aware of. Of course, the most recent ones are often what dominate our attention and can cause alarm or panic about your own health care devices being recalled as well. This includes insulin syringes which were recently found to have problems with their auto-injector needle covers, leading some patients to experience adverse events including pain, skin damage, bleeding, and bruising on injection sites. Many of these are used for people who require daily injections. So there is a great deal at risk here if faulty devices continue causing issues with insertion needles not retracting properly after use.
Abbott has recalled nearly 62,000 pacemakers after finding they have the potential to short circuit. There are some recent medical device recalls on the market that you need to know about. Pacemakers are one of these products, so patients and doctors alike need to understand why this happened.
One reason pacemaker recall has taken place is because there was a lack of communication between manufacturers. However, now that things have changed, this problem should not occur again! Unauthorized personnel may also access information like names and addresses of people who purchased implants before.
In conclusion, here are the top six medical device recalls from the past few years. It’s a good idea to keep up with these major product failures because you never know when it could affect your health care decisions.
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