49 results · 17ms · Sources: EU EUDAMED, US FDA

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Neptune 1 Silver Rover, Part 0700-003-000 Stryker Instruments Neptune Rover IFU part 0700-001-700

FDA Recall
Terminated ·Stryker Instruments Div. of Stryker Corporation·Product code FYD·June 8, 2012

ThermoFlo 1 HME, Disposable, Non-sterile, Expiry date 04/17. Used as a humidifier in a breathing circuit.

FDA Recall
Terminated ·Arc Medical Inc·Product code BYD·February 19, 2015

Stryker brand Neptune waste management system, Neptune Rover, 15 amp plug; model 0700-003-000.

FDA Recall
Terminated ·Stryker Instruments Div. of Stryker Corporation·Product code FYD·October 12, 2004

Portex Thermovent T, Heat and Moisture Exchangers Catalog # 570016;

FDA Recall
Terminated ·Smiths Medical ASD, Inc.·Product code BYD·July 13, 2004

MAQUET Servo Humidifier 163; Model No.: 01-06-8125-8, catalog no. XKC01-06-8125-8. A heat and moisture condenser (artificial nose) is a device intended to be positioned over a tracheotomy (a surgically created opening in the throat) or tracheal tube (a tube inserted into the trachea) to warm and humidify gases breathed in by a patient.

FDA Recall
Terminated ·Teleflex, Inc.·Product code BYD·December 4, 2014

(1) Gibeck Humid-Vent 2S Flex DC, Product #17731, sterile; (2) Gibeck Humid-Vent 2S Flex DC, Product #17732, non-sterile; (3) Gibeck Humid-Vent Filter Compact S with Smooth-Flo/Swivel, Product #19061, sterile; (4) Gibeck Humid-Vent Filter Compact S with Smooth-Flo/Swivel, Product #19062, non-sterile; and (5) Gibeck Humid-Vent Filter Compact S with Flex Tube, Product #19812, non-sterile.

FDA Recall
Open, Classified ·TELEFLEX MEDICAL INC·Product code BYD·April 11, 2022

smiths medical portex, Y' PIECE 15MM, REF 100/276/000

FDA Recall
Open, Classified ·Smiths Medical ASD Inc.·Product code BYD·July 18, 2024

smiths medical portex, Thermovent 1200, 15mm/22mm: a) REF 100/582/000; b) REF 100/582/000JP; c) REF 100/582/000JS

FDA Recall
Open, Classified ·Smiths Medical ASD Inc.·Product code BYD·July 18, 2024

Flamingo Funnel Small, Model Number SQ20012-01

FDA Recall
Open, Classified ·SurgiSmoke Solutions·Product code FYD·March 16, 2026