FDA Device Recalls

Recalls of medical devices, diagnostic equipment, implants, and surgical instruments.

Classification

All Class I Class II Class III

Status

All Ongoing Completed Terminated

Date

All time Past 30 days Past 12 months

Showing 1–9 of 9 recalls for “Listeria”

Class IIOngoing

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

Oxoid Australia Pty Limited

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.

March 3, 2026 · DeviceView details →

Class IIOngoing

Blood Agar,5% Sheep Blood 100/PK, Product Number R01202

Remel, Inc

The products may contain surface and subsurface contamination of Listeria monocytogenes.

July 11, 2025 · DeviceView details →

FDA Device Recalls

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

Blood Agar,5% Sheep Blood 100/PK, Product Number R01202

Blood/MacConkey Biplate 100/PK, Product Number R02049

Strep Selective II Agar, Product Number R01859

Blood/EMB, Levine 100/PK, Product Number R02041

remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use

remel BLOOD AGAR MacCONKEY AGAR BIPLATE, REF R02049, QTY 100, for invitro diagnostic use

VIDAS CLINICAL VIDAS LISTERIA 60T, CATALOG 30700

API LISTERIA 10 STRIPS+10 MEDIA, CATALOG 10300