145 results · 67ms · Sources: EU EUDAMED, US FDA

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BE 183-XXX (EXACT MODEL NUMBER IS UNKNOWN)

FDA Adverse Event
Death ·INSTRUMENTATION INDUSTRIES, INC.·Product code BTL·September 1, 2009

O2 INSTANT FLOW VALVE

FDA Adverse Event
Other ·INSTRUMENTATION INDUSTRIES, INC.·Product code BTM·February 25, 2011

MAGNETIC PEEP VALVE

FDA Adverse Event
Other ·INSTRUMENTATION INDUSTRIES INC.·Product code BYE·June 1, 2000

DISPOSIBLE CLEAR SWIVEL OXYGEN CONNECTOR

FDA Adverse Event
Malfunction ·INSTRUMENTATION INDUSTRIES INC.·Product code BZA·November 5, 2009

FLOW SELECTOR VALVE

FDA Adverse Event
Other ·INSTRUMENTATION INDUSTRIES, INC.·Product code BXY·October 4, 2005

02 INSTANT FLOW VALVE

FDA Adverse Event
Injury ·INSTRUMENTATION INDUSTRIES, INC·Product code BTM·February 10, 2011

N/A

FDA Adverse Event
Death ·INSTRUMENTATION INDUSTRIES, INC·Product code BYE·February 25, 1992

ADULT INLINE MDI ADAPTER

FDA Adverse Event
Malfunction ·INSTRUMENTATION INDUSTRIES, INC.·Product code CCQ·July 1, 2010

Transtracheal (Jet Ventilation) Catheter ACU 1060.1, labeled sterile if unopened. The Jet Ventilation Catheter allows a safe and atraumatic transtracheal access for oxygenation/ventilation.

FDA Recall
Terminated ·Instrumentation Industries Inc·Product code BTO·July 9, 2009

MEDICAL ACTION KIT: ED THORACOTOMY INST.

FDA Adverse Event
Malfunction ·MEDICAL ACTION INDUSTRIES·Product code KDD·December 18, 2015

Ventilator Tubing

FDA Recall
Terminated ·Instrumentation Industries Inc·Product code BTO·September 23, 2015

HYPODERMIC NEEDLE

FDA Adverse Event
CHENGDU SHIFENG MEDICAL TECHNOLOGY CO., LTD.·Product code FMI·December 29, 2022

Instrumentation Industries BE183-SU and BE 183 SU-12 Manual Jet Ventilators; BE 183-SUR and BE 183 SUR-12 Manual Jet Ventilators with Regulator and Gauge; BE 183-2 4 ft. Small Bore Tubing Assembly w/Inline Filter; and BE 183-R Regulator The BE 183-SUR and BE 183-SU Manual Jet Ventilators are designed to provide transtracheal ventilation in specific emergency situations of upper airway obstructions.

FDA Recall
Terminated ·Instrumentation Industries Inc·Product code BTL·September 7, 2012

BTA3D CONTROL MODULE, INDUSTRY - 210148

FDA Adverse Event
Malfunction ·BIOMÉRIEUX, INC.·Product code MDB·November 24, 2021

ENDOWRIST

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·November 27, 2024

MEDLINE INDUSTRIES, INC.

FDA Adverse Event
Malfunction ·MEDLINE INDUSTRIES, INC.·Product code OHD·July 3, 2025

ENDOWRIST

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·September 19, 2024

KIT: CIRCUMCISION 20/CS

FDA Adverse Event
Malfunction ·MEDICAL ACTION INDUSTRIES·Product code OHG·May 11, 2026

KIT: CIRCUMCISION 20/CS

FDA Adverse Event
Malfunction ·MEDICAL ACTION INDUSTRIES·Product code OHG·May 11, 2026

KIT: CIRCUMCISION 20/CS

FDA Adverse Event
Malfunction ·MEDICAL ACTION INDUSTRIES·Product code OHG·May 11, 2026