OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystem
Class I - Dangerous 🏥 Medical Devices
Recalled: March 3, 2026 Oxoid Australia Pty Limited Diagnostic Equipment
Nationwide
What Should You Do?
- Check if you have this product: UDI/DI 5032384127498, Lot Number 4494873
- 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:
- Oxoid Australia Pty Limited
- Reason for Recall:
- Oxoid Ltd., part of Thermo Fisher Scientific, confirmed that Microbact 12L Kit 20 Tests MB1128A lot 4494873 may identify incorrect organism due to inconclusive result from ambiguous color reactions in wells.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystem
Product Codes/Lot Numbers:
UDI/DI 5032384127498, Lot Number 4494873
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1766-2026