FDA Device Intelligence
Home › Avanos Medical, Inc. › Halyard

Halyard

Avanos Medical, Inc. · Model 51743 · UDI-DI 10680651517439

LHC Prescription
10
510(k) clearances
211
Adverse events
10
Recalls
31
Facilities

Description

HYH,WARMER,FLUID,6.6L,1

Recalls

DateFirmReason
2016-10-25Smiths Medical ASD, Inc.Smiths Medical became aware that that one (1) NORMOFLO H-1100 Irrigation Fluid Warmers was incorrectly labelled with Spanish language labels instead of English labels. Specifical
2015-08-25Resource Optimization & Innovation LlcCustom surgical kits contain a component (ORS fluid warming and slush drapes) that was recalled due to compromised package integrity potentially affecting sterility assurance.
2015-08-25Resource Optimization & Innovation LlcCustom surgical kits contain a component (ORS fluid warming and slush drapes) that was recalled due to compromised package integrity potentially affecting sterility assurance.
2015-08-25Resource Optimization & Innovation LlcCustom surgical kits contain a component (ORS fluid warming and slush drapes) that was recalled due to compromised package integrity potentially affecting sterility assurance.
2015-08-25Resource Optimization & Innovation LlcCustom surgical kits contain a component (ORS fluid warming and slush drapes) that was recalled due to compromised package integrity potentially affecting sterility assurance.
2015-08-25Resource Optimization & Innovation LlcCustom surgical kits contain a component (ORS fluid warming and slush drapes) that was recalled due to compromised package integrity potentially affecting sterility assurance.
2015-08-25Resource Optimization & Innovation LlcCustom surgical kits contain a component (ORS fluid warming and slush drapes) that was recalled due to compromised package integrity potentially affecting sterility assurance.
2015-08-25Resource Optimization & Innovation LlcCustom surgical kits contain a component (ORS fluid warming and slush drapes) that was recalled due to compromised package integrity potentially affecting sterility assurance.
2015-08-25Resource Optimization & Innovation LlcCustom surgical kits contain a component (ORS fluid warming and slush drapes) that was recalled due to compromised package integrity potentially affecting sterility assurance.
2015-08-18Ecolab IncThe sterile packaging may contain small (less than 250 microns wide) channels in the seal of the pouch. If channels are present, the package integrity is compromised and there is a

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
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.