FDAClass IIApril 8, 2026

Oxoid Microbact Identification Kits recall

OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystem

Why was Oxoid Microbact Identification Kits recalled?

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.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

UDI/DI 5032384127498, Lot Number 4494873

Product
OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Tests; Listeria identification sysystem
Recalling firm
Oxoid Australia Pty Limited
Quantity
2 kits
Distribution
US Nationwide distribution in the states of GA and CA.
Recall date
April 8, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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