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Updated 2026-04-08

Oxoid Australia Pty Limited recalls OXOID MICROBACT IDENTIFICATION KITS, Listeria 12L Kit, 20 Te

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Recalled Product

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

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Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI/DI 5032384127498, Lot Number 4494873

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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