🔍 RecallPedia

Admelog Solostar (insulin lispro injection), 100 units/ mL (U-100) injection, packaged in 3mL prefilled pens, 1 pen per box, Rx only, Physician Sample - Not For Sale, Sanofi-Aventis U.S. LLC, Bridgewater, NJ 08807, NDC 0024-5925-00

Class I - Dangerous
💊 Drugs Recalled: July 5, 2018 Sanofi-Aventis U.S. Prescription Drugs Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot #: 7F021B, Exp 6/30/20
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Sanofi-Aventis U.S. LLC
Reason for Recall:
Temperature Abuse: Product samples of Admelog may not have been shipped at proper temperature.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

Admelog Solostar (insulin lispro injection), 100 units/ mL (U-100) injection, packaged in 3mL prefilled pens, 1 pen per box, Rx only, Physician Sample - Not For Sale, Sanofi-Aventis U.S. LLC, Bridgewater, NJ 08807, NDC 0024-5925-00

Product Codes/Lot Numbers:

Lot #: 7F021B, Exp 6/30/20

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-0925-2018

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