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

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A2814 SPINAL (SDD)W/DRUGS

FDA Recall
Terminated ·Smiths Medical ASD, Inc.·Product code CAZ·July 2, 2004

A2837 SPINAL(SDD)W/DRUGS

FDA Recall
Terminated ·Smiths Medical ASD, Inc.·Product code CAZ·July 2, 2004

A3077-25 SPINAL (SDD) W/DRUGS

FDA Recall
Terminated ·Smiths Medical ASD, Inc.·Product code CAZ·July 2, 2004

A3015-25 SPINAL (SDD) W/DRUGS

FDA Recall
Terminated ·Smiths Medical ASD, Inc.·Product code CAZ·July 2, 2004

A2291-27 SPINAL (SDD) W/DRUGS

FDA Recall
Terminated ·Smiths Medical ASD, Inc.·Product code CAZ·July 2, 2004

A3075-25 SPINAL (SDD) W/DRUGS

FDA Recall
Terminated ·Smiths Medical ASD, Inc.·Product code CAZ·July 2, 2004

A2957 SPINAL (SDD) W/DRUGS K516566

FDA Recall
Terminated ·Smiths Medical ASD, Inc.·Product code CAZ·July 2, 2004

A3121-25 SPINAL (SDD) W/DRUGS

FDA Recall
Terminated ·Smiths Medical ASD, Inc.·Product code CAZ·July 2, 2004

A2624-22/25 SPINAL (SDD) W/DRUGS

FDA Recall
Terminated ·Smiths Medical ASD, Inc.·Product code CAZ·July 2, 2004

A3065-25 SPINAL TRAY (SDD) W/DRUGS

FDA Recall
Terminated ·Smiths Medical ASD, Inc.·Product code CAZ·July 2, 2004

A2832-25 SPINAL TRAY (SDD) W/ DRUGS

FDA Recall
Terminated ·Smiths Medical ASD, Inc.·Product code CAZ·July 2, 2004

15995-20 SPINAL(SDD)25G QUINCKE W/DRUGS

FDA Recall
Terminated ·Smiths Medical ASD, Inc.·Product code CAZ·July 2, 2004

Smiths Medical ASD, Inc. Regional Anesthesia Trays containing the Hospira 2ml drug ampuls of 5% Lidocaine Hydrochloride with 7.5% Dextrose Injection, (NDC 0074-4712-01, lot number 09-568-DK) as follows: Product Number/Description 15248C-22/25 SPINAL TRAY 22/25 (SDD)W/DRUGS

FDA Recall
Terminated ·Smiths Medical ASD, Inc.·Product code CAZ·July 2, 2004

Dual Delivery 4DD-1 of GYC-1000 Green Laser Photocoagulator system GYC4DD-1: The Nidek Green Laser Photocoagulator Model GYC- 1000 is indicated for use in ophthalmic surgical procedures, including retinal and macular photocoagulation, iridotomy and trabeculoplasty.

FDA Enforcement
Class II ·Terminated·Nidek Inc·July 22, 2015

AIA-PACK B12 Pretreatment Set- IVD for diagnostic use for pre-treatment of calibrators/controls. Part Number: 020706

FDA Enforcement
Class III ·Terminated·Tosoh Smd Inc·January 1, 2020

AIA Analyzer Pipette Tips used on Tosoh AIA-2000, AIA-1800, AIA-900 and AIA-600II Analyzers, 1000 tips/bag AIA-Analyzer Tips are disposable pipette tips packaged in bulk quantities and used on Tosoh Bioscience AIA Analyzers for lab analysis of various immunoassays.

FDA Enforcement
Class II ·Terminated·Tosoh Smd Inc·August 7, 2013

Keyspan High-High Speed USB to Serial Adapter Product Usage: The Reporting Software is an application which serves as middle ware between the Tosoh Automated HPLC G8 analyzer and an LIS or as a stand alone data repository for the analyzer. It is designed to store and manage the received data and make reports as necessary. The application is installed on Dell All- in-One computers that do not have serial (RS232) ports only USB ports. The G8 analyzer does not have USB ports. The Key Span Adaptor connects the serial port on the G8 to the USB port on the Dell computer. Once installed the Keyspan adapter is assigned a COM port. The default for the firmware is dynamic which randomly assigns a port for the transmission of data. The port assignment can change when the power for the analyzer or computer is shut down or the cable is physically disconnected and then reconnected. The default can be changed to geographic which allows the port assignment to be static regardless of a power outage.

FDA Enforcement
Class II ·Terminated·Tosoh Smd Inc·March 1, 2017

AmerisourceBergen PF Latex SG (Surgical Glove), Sterile, Powder Free, Size 6.5, Item No. 10112

FDA Enforcement
Class II ·Terminated·WRP Asia Pacific Sdn Bhd·June 6, 2018

Stryker brand Firstcare Ultra Maternity bed and Stryker brand Adel Maternity bed, 220 volt, model 5012, with night light.

FDA Recall
Terminated ·Stryker Medical·Product code HDD·January 26, 2004

Siemens Dimension Vista(R) System B12 Flex(R) Reagent Cartridge (K6442) B12 Flex Reagent Cartridge used with the Dimension Vista System for the in vitro diagnostic test for the quantitative measurement of Vitamin B12 in human serum and plasma.

FDA Recall
Terminated ·Siemens Healthcare Diagnostics, Inc.·Product code CDD·May 8, 2012