889 results · 20ms · Sources: EU EUDAMED, US FDA

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Eclipse Blood Collection Set

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

IDENT-A100 INTRAORAL VIDEO CAMERA

FDA 510(k)
FDA Class 1 ·Dental

GE LOGIQ I, LOGIQ E AND VIVID E

FDA 510(k)
FDA Class 2 ·Radiology

DISOPA SOLUTION

FDA Adverse Event
Malfunction ·JOHNSON & JOHNSON, JAPAN·Product code MED·October 23, 2008

COLLEAGUE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 16, 2011

INSIGNIA

FDA Adverse Event
Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 9, 2013

MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213805, K220425, K231560.

FDA Recall
Open, Classified ·Siemens Medical Solutions USA, Inc·Product code LNH·August 28, 2025

MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213805, K220425, K231560.

FDA Enforcement
Class I ·Ongoing·Siemens Medical Solutions USA, Inc·October 8, 2025

BD VACUTAINER® K2 EDTA (K2E) 3.6MG BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·May 26, 2026

BD VACUTAINER® K2 EDTA (K2E) 3.6MG BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·May 1, 2026

BD VACUTAINER® K2 EDTA (K2E) 5.4MG BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·April 28, 2026

BD VACUTAINER® K2 EDTA (K2E) 5.4MG BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·March 11, 2026

BD VACUTAINER® K2 EDTA (K2E) 3.6MG BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·May 12, 2026

BD VACUTAINER® K2 EDTA (K2E) 5.4MG BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·May 15, 2026

BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·February 5, 2026

BD VACUTAINER® K2 EDTA (K2E) 5.4MG BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·May 14, 2026

BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·February 6, 2026

BD VACUTAINER® K2 EDTA (K2E) 10.8MG BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·May 12, 2026

BD VACUTAINER® K2 EDTA (K2E) 3.6MG BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·May 1, 2026

BD VACUTAINER® K2 EDTA (K2E) 7.2MG BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code GIM·February 23, 2026