It poses a serious health hazard.
According to the recall notice, the company pulled the insulin pens after discovering they could be missing a label.As the product is a long-acting insulin used by adults and children to improve glycemic control in patients with type 1 diabetes or adults with type 2 diabetes, the FDA warns that patients who may use more than one type of insulin for their treatment could mix up the products and use the wrong strength, potentially resulting in"serious complications.
Anyone with questions about the recall can also reach the customer relations division of parent company Viatris by calling 1-800-796-9526 on weekdays between 8 a.m. and 5 p.m. EST or emailing [email protected]. The agency also urges patients who believe they're experiencing any health problems related to the recalled product to call their doctor or healthcare provider immediately.Zach is a freelance writer specializing in beer, wine, food, spirits, and travel.
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