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CirQPOD Blower

Zoll Medical Corporation · Model 12-2403-000 · UDI-DI 00847946028343

BWF
10
510(k) clearances
180
Adverse events (4 deaths)
1
Recalls
53
Facilities

Description

CIRQPOD BLOWER

Recalls

DateFirmReason
2020-12-21Smiths Medical ASD Inc.Shipping box may contain wrong model.

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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.