remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI/DI 848838003684, Lot Number 213971, exp. 2025-02-25
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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 EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use
Product Codes/Lot Numbers:
UDI/DI 848838003684, Lot Number 213971, exp. 2025-02-25
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1201-2025
Related Recalls
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.
Products may contain contamination, which may result in a darker or brown media color.
The products may contain surface and subsurface contamination of Listeria monocytogenes.