HemoTrol Level 3- In Vitro Diagnostic Hematology quality control mixture. Catalogue number: 171.003.002 Eurotrol HemoLin is an assayed hemoglobin control intended for professional use in the verification of the linearity of the HemoCue¿ Hb 201 systems.

Class I - Dangerous
🏥 Medical Devices Recalled: October 18, 2018 EUROTROL Diagnostic Equipment Nationwide

What Should You Do?

  1. Check if you have this product:
    Batch Number: 82467
  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:
EUROTROL INC
Reason for Recall:
Incorrect measurement results caused by microbial contamination of the product, results in values lower than assigned values
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

HemoTrol Level 3- In Vitro Diagnostic Hematology quality control mixture. Catalogue number: 171.003.002 Eurotrol HemoLin is an assayed hemoglobin control intended for professional use in the verification of the linearity of the HemoCue¿ Hb 201 systems.

Product Codes/Lot Numbers:

Batch Number: 82467

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0515-2019

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