Recall of Humalog KwikPen U-100
On May 25, 2022, the U.S. Food and Drug Administration (FDA) announced that Cardinal Health is voluntarily recalling Humalog KwikPen U-100 as a Class I Recall. The products were exposed to temperatures outside of the labeled storage conditions due to inclement weather.
Your health and safety are important to us. If you are currently taking Humalog KwikPen U-100, please contact your health care provider to talk about other treatments or medicines that may be appropriate.
For more information, please visit FDA.gov. If you have questions about this recall, the Horizon NJ Health Pharmacy Help Desk is available at 1-800-682-9094 x81016 (TTY 711), weekdays, 8 a.m. to 5 p.m., Eastern Time.