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JELCO HYPODERMIC NEEDLE-PRO FIXED NEEDLE INSULIN SYRINGE: a) 1.0mL 28G X 1/2" (0.33mm x 13mm), REF 4428-1 b) 1.0mL 29G X 1/2" (0.33mm x 13mm), REF 4429-1

FDA Enforcement
Class I ·Terminated·Smiths Medical ASD Inc.·June 16, 2021

Streamline MIS Spinal Fixation System Fixed Rod Holder NON STERILE, Rx only The Streamline MIS Spinal Fixation System is intended for posterior, noncervical pedicle fixation, T1-S2. Pedicle screw fixation is limited to skeletally mature patients and is intended to be used as an adjunct to fusion. The device is indicated for all the following indications: degenerative disc disease (ODD) (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies); spondylolisthesis; trauma (i.e. fracture or dislocation); spinal stenosis; deformities or curvatures (i.e. scoliosis, kyphosis, and /or lordosis); tumor; pseudoarthrosis; and failed previous fusion. The Streamline MIS instrumentation, when used with the Streamline MIS Spinal Fixation System, is indicated to provide the surgeon with a minimally invasive approach for posterior spinal surgery.

FDA Enforcement
Class II ·Terminated·PIONEER SURGICAL TECHNOLOGY, INC.·September 17, 2014

JELCO HYPODERMIC NEEDLE-PRO FIXED NEEDLE INSULIN SYRINGE: a) 1.0mL 28G X 1/2" (0.33mm x 13mm), REF 4428-1 b) 1.0mL 29G X 1/2" (0.33mm x 13mm), REF 4429-1

FDA Recall
Terminated ·Smiths Medical ASD Inc.·Product code MEG·May 17, 2021

PROBEAT-V, software versions 4.8.1S, and 5.1M Radiation therapy system.

FDA Recall
Terminated ·Hitachi America, Ltd., Power Systems Division·Product code LHN·April 15, 2019

Streamline MIS Spinal Fixation System Fixed Rod Holder NON STERILE, Rx only The Streamline MIS Spinal Fixation System is intended for posterior, noncervical pedicle fixation, T1-S2. Pedicle screw fixation is limited to skeletally mature patients and is intended to be used as an adjunct to fusion. The device is indicated for all the following indications: degenerative disc disease (ODD) (defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies); spondylolisthesis; trauma (i.e. fracture or dislocation); spinal stenosis; deformities or curvatures (i.e. scoliosis, kyphosis, and /or lordosis); tumor; pseudoarthrosis; and failed previous fusion. The Streamline MIS instrumentation, when used with the Streamline MIS Spinal Fixation System, is indicated to provide the surgeon with a minimally invasive approach for posterior spinal surgery.

FDA Recall
Terminated ·PIONEER SURGICAL TECHNOLOGY, INC.·Product code NKB·June 14, 2013

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

IMMULITE /IMMULITE 1000 Vitamin B12

FDA Recall
Terminated ·Siemens Healthcare Diagnostics, Inc.·Product code CDD·January 2, 2018

Stryker brand Firstcare Ultra Maternity bed, model 5010, with night light.

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

Sample Management System software for in vitro diagnostic testing Product # 030102-03

FDA Recall
Terminated ·Siemens Medical Solutions Diagnostics·Product code CDD·January 15, 2007

VITROS Immunodiagnostic Products Vitamin B12 Reagent Pack 1/2, Catalog Number 1453489 For in vitro diagnostic use only For the quantitative measurement of vitamin B12 in human serum and plasma (EDTA or heparin) using the VITROS ECi/ECiQ Immunodiagnostic Systems, the VITROS 3600 Immunodiagnostic System and the VITROS 5600 Integrated System, to aid in the differential diagnosis of anemia

FDA Recall
Terminated ·Ortho-Clinical Diagnostics·Product code CDD·August 28, 2018

AVE 2 Birthing Bed

FDA Recall
Terminated ·Linet Spol. S.r.o. Zelevcice 5 Slany Czech Republic·Product code HDD·January 7, 2019

Hill-Rom Affinity Four Birthing Bed, Hill-Rom Company, Inc., Batesville, Indiana; Model P3700B. Intended to be used as birthing beds for momen of child bearing age in an labor, delivery, recovery or postpartum setting in acute care.

FDA Recall
Terminated ·Hill-Rom, Inc.·Product code HDD·November 16, 2009

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

FDA Recall
Terminated ·Tosoh Smd Inc·Product code CDD·November 15, 2019

AIA-PACK B12 (Vitamin B12) is designed for IN VITRO DIAGNOSTIC USE ONLY for the quantitative measurement of vitamin B12 (B12) in human serum on Tosoh AIA System analyzers.

FDA Recall
Terminated ·Tosoh Bioscience Inc·Product code CDD·November 30, 2018

Stryker brand Birthing Bed; Model 4701.

FDA Recall
Terminated ·Stryker Medical·Product code HDD·March 31, 2005

Hill-Rom Affinity 4 Birthing Bed; Model P3700B, Hill-Rom, Inc., Batesville, IN 47006

FDA Recall
Terminated ·Hill-Rom, Inc.·Product code HDD·September 6, 2007

Stryker brand Adel maternity bed, model 4700, with night light.

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

IMMULITE 2000 Vitamin B12 Kit, Catalog # L2KVB2, L2KVB6, kit lot 186.

FDA Recall
Terminated ·Diagnostic Products Corp·Product code CDD·January 24, 2005

CA 15-3 Calibrators, list 9C08-01; the pack contains six 4-mL bottles of 115D8:DF3 reactive determinants prediluted in TRIS buffer with protein stabilizers to yield the following assay values: A - 0 u/mL, B - 15 U/mL, C - 60 U/mL, D - 120 U/mL, E - 180 U/mL and F - 250 U/mL; Abbott Laboratories, Abbott Park, IL 60064

FDA Recall
Terminated ·Abbott Laboratories HPD/ADD·Product code MOI·March 4, 2003