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EC10-120MD

ASTEC CO.,LTD. · Model EC10-120MD · UDI-DI 04580647510125

PUB
1
510(k) clearances
5
Adverse events
6
Recalls
21
Facilities

Recalls

DateFirmReason
2024-11-15CooperSurgical, Inc.The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will al
2024-11-15CooperSurgical, Inc.The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will al
2024-11-15CooperSurgical, Inc.The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will al
2024-11-15CooperSurgical, Inc.The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will al
2024-11-15CooperSurgical, Inc.The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will al
2024-11-15CooperSurgical, Inc.The warming surfaces or incubator well temperatures of the listed products may exceed the desired set temperature. If temperatures exceed the desired set value, the device will al

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.