remel BLOOD AGAR MacCONKEY AGAR BIPLATE, REF R02049, QTY 100, for invitro diagnostic use

Class I - Dangerous
🏥 Medical Devices Recalled: February 13, 2025 Remel Diagnostic Equipment Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI/DI 848838003691, Lot Number 213926, exp. 2025-02-24
  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:
Remel, Inc
Reason for Recall:
Product may contain surface and subsurface contamination of Listeria monocytogenes which is typically visible immediately upon removal from the packaging, appearing on the blood side of the biplate.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

remel BLOOD AGAR MacCONKEY AGAR BIPLATE, REF R02049, QTY 100, for invitro diagnostic use

Product Codes/Lot Numbers:

UDI/DI 848838003691, Lot Number 213926, exp. 2025-02-24

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1200-2025

Related Recalls

Class I - Dangerous

Products may report incorrect AST results during quality control. Health consequences may include delayed response or the need to change to another antifungal agent if laboratory ignores Quality Control test result.

Mar 24, 2026 Other Medical Devices Nationwide View Details →