FDAFDA · Food and drugs·Recall number Z-1201-2025
remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use
Published February 26, 2025 · Recall initiated: February 13, 2025
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Remel, Inc
- Distributor
- US Nationwide distribution.
- Lot
- UDI/DI 848838003684, Lot Number 213971, exp. 2025-02-25
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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