Recall: NovoPen Echo Insulin Delivery Device
On 2017-07-06, the FDA announced that Novo Nordisk is conducting a recall on Insulin Delivery Device due to a possible defect. The recalled products were sold under the brand name(s) NovoPen Echo during an unspecified time period throughout the regions shown in the map below.
In recent months, there have been 5 medical devices recalls due to potential defect, including catheters, intra-aortic balloon pumps and more. Additionally, there have been 3 drug and medical device recalls due to other health hazards as well as 141 food recalls.
Company Contact Information:
Name: Novo Nordisk
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Detailed Recall Information
Regions Where Sold: Because the region was not specified, it is assumed that this product was available nationwide.
Product Description: Insulin delivery device
Brand Name(s): NovoPen Echo
Reason for Recall: Device may crack or break if exposed to certain chemicals
Official Recall Date: 2017-07-05
Note: Although this recall announcement is dated 07/05/2017, it was not published by the FDA until 07/06/2017.
Additional information provided by the FDA.gov:
Novo Nordisk is initiating a recall of insulin cartridge holders used in a small number of NovoPen Echo batches because they may crack or break if exposed to certain chemicals, like certain cleaning agents. NovoPen Echo is used for insulin treatment by people with diabetes. Using a device with a cracked/broken cartridge holder may result in the device delivering a reduced dose of insulin which could potentially lead to high blood sugar. Novo Nordisk believes the risk of experiencing high blood sugar when using a device with an affected cartridge holder is low. Read More.
More information may be available at FDA.gov
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Sources may include Food & Drug Administration (FDA), United States Department of Agriculture (USDA), Health Canada and companies involved with this or a related recall.