remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use
Reported: February 26, 2025 Initiated: February 13, 2025 #Z-1201-2025
Product Description
remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use
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.
Details
- Recalling Firm
- Remel, Inc
- Units Affected
- 316 units
- Distribution
- US Nationwide distribution.
- Location
- Lenexa, KS
Frequently Asked Questions
What product was recalled? ▼
remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use. Recalled by Remel, Inc. Units affected: 316 units.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 26, 2025. Severity: Moderate. Recall number: Z-1201-2025.
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