The Food and Drug Administration has issued a recall for an insulin pump that thousands of people use with Type 1 diabetes.
The recall is centered around certain Medtronic MiniMed 600 series insulin pumps.
One person has died, 2,175 people have received injuries and there have been more than 26,000 complaints, according to a statement released by the FDA.
Medtronic is recalling the specified insulin pumps due to a missing or broken retainer ring. That ring helps lock the insulin cartridge into place, according to the FDA.
More
DelMarVa's Premier Source for News, Opinion, Analysis, and Human Interest Contact Publisher Joe Albero at alberobutzo@wmconnect.com or 410-430-5349
2 comments:
Little old news this was in June last year..........
12:47
Look again. How can it be for June of 2019 when Medtonic notified customers in November 2019.
The press release from the FDA is dated 2/12/2020
The date on the article from Fox 45 is February 13th.
Where do you see June of last year?
Post a Comment