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Home › FDA recalls › OXOID MICROBACT IDENTIFICATION KITS
CLASS II · ModerateFDA

Oxoid Australia Pty Limited recalls OXOID MICROBACT IDENTIFICATION KITS

📅 Mar 3, 2026 · 📍 Nationwide
Recalling company
Oxoid Australia Pty Limited
Product
OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystem
Reason
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 II – may cause temporary or medically reversible health consequences
Recall date
Mar 3, 2026
Reported
Apr 8, 2026
Distribution
US Nationwide distribution in the states of GA and CA.
Status
Ongoing
Quantity
2 kits
Lot / codes
UDI/DI 5032384127498, Lot Number 4494873
Company location
South Australia
Recall type
Voluntary: Firm initiated
Recall number
Z-1766-2026
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-1766-2026 in the FDA Enforcement Report. Also see FDA recall press releases.

If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.