23 results · 14ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Brand Name: OBM00002 OBM DAB (Digital Acquisition Box) Product Name: OBM00002 OBM DAB (Digital Acquisition Box) Model/Catalog Number: OBM00002 OBM DAB (Digital Acquisition Box) Software Version: N/A Product Description: OBM00002 OBM DAB (Digital Acquisition Box) Component: No

FDA Recall
Open, Classified ·Natus Neurology DBA Excel Tech., Ltd. (XLTEK)·Product code OMA·May 7, 2025

Moberg Component Neuromonitoring System (CNS Monitor)-Intended as a short-term neurological monitoring system that collects, displays, and stores multiple physiological measurements Model: CNS-350

FDA Recall
Open, Classified ·Moberg Research, Inc.·Product code OMA·February 20, 2023

VNS Therapy Programmer, Model 3000 used with Models 103, 104, 105, 106, or 8103 VNS Therapy generators.

FDA Recall
Open, Classified ·LivaNova USA Inc·Product code LYJ·February 4, 2020

Cryo Module Accessories Domestic CMA-OUS, Product Catalog Number A001053

FDA Recall
Open, Classified ·AtriCure, Inc.·Product code GEH·November 28, 2023

Packaged, Tank Hose Assembly CMA-US, Product Catalog Number A001056

FDA Recall
Open, Classified ·AtriCure, Inc.·Product code GEH·November 28, 2023

Recreo Hair Growth Laser Comb

FDA Recall
Open, Classified ·OMM Imports, Inc. dba Zero Gravity·Product code OAP·September 1, 2022

VNS Therapy Program GMDN: 44077 Model # 3000 V1.5.2, RxOnly

FDA Recall
Open, Classified ·LivaNova USA Inc·Product code LYJ·November 16, 2018

MediBeads Neck Wrap, Item Number 34320

FDA Recall
Open, Classified ·Bruder Healthcare Company, LLC·Product code IMA·February 21, 2024

PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic glue.

FDA Recall
Open, Classified ·Preat Corp·Product code EMA·February 1, 2023

IonoStar Plus, Catalog (REF) Numbers: a) 2540, b)2543, c) 2544, d) 2545, e) 2546, f) 2547, g) 2549; dental cement

FDA Recall
Open, Classified ·Voco GmbH Anton-Flettner-Str. 1-3 Cuxhaven Germany·Product code EMA·January 25, 2024

Thermalon Eye Compress, Item Number 2434

FDA Recall
Open, Classified ·Bruder Healthcare Company, LLC·Product code IMA·February 21, 2024

Thermalon Neck Wrap, Item Number 24322

FDA Recall
Open, Classified ·Bruder Healthcare Company, LLC·Product code IMA·February 21, 2024

Thermalon Stye Compress, Item Number 24352

FDA Recall
Open, Classified ·Bruder Healthcare Company, LLC·Product code IMA·February 21, 2024

Thermalon Heating Pad, Item Number 24002

FDA Recall
Open, Classified ·Bruder Healthcare Company, LLC·Product code IMA·February 21, 2024

DENTEMP ONE STEP .077OZ, SKU 902139

FDA Recall
Open, Classified ·Family Dollar Stores, Llc.·Product code EMA·October 4, 2023

Ionolux, Catalog (REF) Numbers: a) 2115, b)2117, c) 2118, d) 2119, e) 2120, f) 2122; dental cement

FDA Recall
Open, Classified ·Voco GmbH Anton-Flettner-Str. 1-3 Cuxhaven Germany·Product code EMA·January 25, 2024

MediBeads King Pad, Item Numbers: 34120, 34120PM, 34125R

FDA Recall
Open, Classified ·Bruder Healthcare Company, LLC·Product code IMA·February 21, 2024

Thermalon Sinus Compress, Item Number 24332

FDA Recall
Open, Classified ·Bruder Healthcare Company, LLC·Product code IMA·February 21, 2024

Thermalon Back Wrap, Item Number 24312

FDA Recall
Open, Classified ·Bruder Healthcare Company, LLC·Product code IMA·February 21, 2024

DENTEMP ONE STEP .077OZ, SKU 902139

FDA Recall
Open, Classified ·Family Dollar Stores, Llc.·Product code EMA·June 23, 2022