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Home Medical Products Inc.

Manufacturer
🇹🇼 Taiwan·1 Importer

Home Medical Products Inc.

FDA registration
Home Medical Products Inc.·12 products·🇹🇼 Taiwan

LUMEX

FDA Adverse Event
Injury ·HOME MEDICAL PRODUCTS, INC.·Product code FSA·January 25, 2019

Algol Trehab Oy

Importer
🇫🇮 Finland·2 Manufacturers

CORFLO NG/NI FEED TUBE WITH STYLET, ENFIT CONNECTOR

FDA Adverse Event
Malfunction ·AVANOS MEDICAL INC.·Product code KNT·May 28, 2026

MIC PERCUTANEOUS ENDOSCOPIC GASTROSTOMY PEG KIT

FDA Adverse Event
Malfunction ·AVANOS MEDICAL INC.·Product code KNT·May 1, 2026

Cordis a Johnson & Johnson Company, RadialSource Spring Wire Transradial Access Kit. Manufacturer Greatbatch Medical 2300 Berkshire Lane North, Minneapolis, MN 55441, Distributor Cordis Corporation 14201 North West 60th Avenue, Miami Lakes, Florida 33014. Baxter's lnfusors SV Elastomeric Infusion Device is a single-use, disposable elastomeric infusion pump indicated tor patients requiring slow, continuous intravenous, intra-arterial, subcutaneous, or epidural administration of medications at a constant flow rate. The device is also indicated for the administration of bolus doses of medication upon patient demand when used in conjunction with the Patient Control Module. lt is suitable for use in the hospital or home setting.

FDA Enforcement
Class II ·Terminated·Greatbatch Medical·July 3, 2013

HOMEPUMP C-SERIES, 270 ML, 5 ML/HR (CONTAINS DEHP)

FDA Adverse Event
Malfunction ·AVANOS MEDICAL INC.·Product code MEB·April 11, 2024

CADD

FDA Adverse Event
Malfunction ·ST PAUL·Product code FPA·April 16, 2020

Salter Labs Bubble humidifier, with 6 PSI safety valve, 350cc, Latex Free; Single Patient use; used with supplemental oxygen therapy. Model Numbers 7600-0-50, E7600-0-50, NP7600-0-50 and special order patient kits that contain 7600 humidifiers. Patient kits have brand names of Salter Labs, AdvaCare; Allcare Medical; Memorial Home Services; Therapy Support Inc; Mendo-Lake Home Respiratory Services; MedAssurance Inc.; Abundant Home Care. Product Usage: Humidifier - single patient use. used with supplemental oxygen therapy.

FDA Recall
Terminated ·SALTER LABS·Product code BBT·October 21, 2011

O-ARM 1000 IMAGING SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC. (LITTLETON)·Product code OXO·November 1, 2016

ON-Q PUMP WITH SELECT-A-FLOW

FDA Adverse Event
Injury ·AVANOS MEDICAL INC.·Product code MEB·July 14, 2023

UNO 102 EE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FSA·February 5, 2025

UNKNOWN NASOGASTRIC/NASOINTESTINAL FEEDING TUBES

FDA Adverse Event
Malfunction ·AVANOS MEDICAL INC.·Product code KNT·December 23, 2025

AIA-900

FDA Adverse Event
Malfunction ·TOSOH CORPORATION·Product code KHO·November 16, 2018

UNKNOWN ON-Q PAIN PUMP

FDA Adverse Event
Injury ·AVANOS MEDICAL INC.·Product code MEB·September 24, 2024

STROLLER

FDA Adverse Event
Injury ·CAIRE INC.·Product code BYJ·June 30, 2021

MIC GASTRIC-JEJUNAL FEEDING TUBE KIT WITH ENFIT CONNECTOR

FDA Adverse Event
Malfunction ·AVANOS MEDICAL INC.·Product code KNT·April 23, 2026

MIC-KEY LOW-PROFILE TRANSGASTRIC-JEJUNAL FEEDING TUBE, 18 FR, 3.0 CM, 45 CM

FDA Adverse Event
Malfunction ·AVANOS MEDICAL INC.·Product code KNT·October 15, 2018

ON-Q C-BLOC INTL PAIN RELIEF SYSTEM WITH ONDEMAND, 400 ML X 5 ML/HR + 5 ML PCA

FDA Adverse Event
Malfunction ·AVANOS MEDICAL - IRVINE·Product code MEB·January 3, 2019