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PRIMED

priMED Medical Products Inc · Model PM4-314 · UDI-DI 00842942017315

FCX
10
510(k) clearances
540
Adverse events (6 deaths)
2
Recalls
33
Facilities

Description

ASTM Level 2 Anti-Fog Strip Mask, Ultra Soft Ear Loops, Blue

Recalls

DateFirmReason
2021-01-15Northgate Technologies, Inc.An internal tubing component in the flow path was made with incorrect material which was not tested for use with this device.
2013-09-16Pentax Medical CompanyPENTAX Medical has become aware of a product issue associated with the OF-B194 Gas/Water Feeding Valve. A manufacturing defect may cause improper stoppage of CO2 gas during an end

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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.