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Critical recall: Death or serious injury has been reported or is considered likely. Stop using this product now.

Cardinal Health Inc. 2022-05-25 Health critical FDA
Health · FDA · Recall #FDA-D-0882-2022

Humalog KwikPen, Insulin lispro injection, U-100, 100 units per mL, 5x3 mL Prefilled Pens… Recall

Issued May 25, 2022 · Cardinal Health Inc.

In May 2022, Cardinal Health Inc. recalled the Humalog KwikPen, Insulin lispro injection, U-100, 100 units per mL, 5x3 mL Prefilled Pens…, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.

Compiled by Maya Ellison, RecallCheckr

What this means for you

TEMPERATURE ABUSE: Products were exposed to temperatures outside of the products labeled storage conditions due to inclement weather.

What you should do

  1. 1 Stop using Humalog KwikPen, Insulin lispro injection, U-100, 100 units per mL, 5x3 mL Prefilled Pens… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Cardinal Health Inc. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Cardinal Health Inc.
Category
Health
Recall date
May 25, 2022
Units affected
Not reported
Sold at
NM only
Recall number
FDA-D-0882-2022
Made in
United States
Issuing agency
FDA

In context

  • Cardinal Health Inc. has 8 recalls in our database, including 4 rated Critical.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 870th Health recall we've logged in 2022.
Read the official FDA notice

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