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Mohs Closer Pack, kit number PSS1827(A, PSS1827(B, and PSS1827(C convenience custom kits used for general surgery in hospital operating room

FDA Enforcement
Class II ·Terminated·Windstone Medical Packaging, Inc.·October 26, 2016

Persona Trabecular Metal Tibia; Persona Trabecular Metal Tibial Plate Instruments and Modular Brackets; Used to facilitate the implantation of joint replacement implants.

FDA Enforcement
Class II ·Terminated·Zimmer Biomet, Inc.·June 15, 2016

Anchored Lateral Retractable Drill, Timberline IPF IFU IFU8621-0113, Model 8630-0102. Timberline Anchored Lateral Retractable Drills are used with the Timberline MPF System to establish access into the vertebrae for the screws utilized to anchor the plate to the vertebrae.

FDA Enforcement
Class II ·Terminated·Biomet Spine, LLC·January 21, 2015

ConvaTec Flexi-Seal SIGNAL +, Rx Only Product Usage: For use to manage fecal incontinence through the collection of liquid to semi-liquid stool and to provide access to administer medication.

FDA Enforcement
Class III ·Terminated·Convatec Inc.·August 28, 2013

ConvaTec Flexi-Seal SIGNAL Fecal Management System, Rx Only Product Usage: For use to manage fecal incontinence through the collection of liquid to semi-liquid stool and to provide access to administer medication.

FDA Enforcement
Class III ·Terminated·Convatec Inc.·August 28, 2013

epoc BGEM Test Card (Catalogue number CT-1004-00-00). quantitative testing of samples for pH, pCO2, pO2, Sodium Potassium , Ionized Calcium, Glucose, Lactate and Hematocrit.

FDA Enforcement
Class II ·Terminated·Epocal·August 21, 2013

ConvaTec Flexi-Seal SIGNAL +, Rx Only Product Usage: For use to manage fecal incontinence through the collection of liquid to semi-liquid stool and to provide access to administer medication.

FDA Recall
Terminated ·Convatec Inc.·Product code KNT·June 25, 2013

ConvaTec Flexi-Seal SIGNAL Fecal Management System, Rx Only Product Usage: For use to manage fecal incontinence through the collection of liquid to semi-liquid stool and to provide access to administer medication.

FDA Recall
Terminated ·Convatec Inc.·Product code KNT·June 25, 2013

S-LIFT Slap Hammer, Part Number: 11-50204, Revision A The slap hammers are used primarily to remove trial instruments that are used to estimate sizes of intervertebral body fusion devices intended to promote fusion. These devices were used in conjunction with lumbar intervertebral body fusion device intended for intervertebral body fusion of the spine of skeletally mature patients.

FDA Recall
Terminated ·SpineFrontier, Inc.·Product code FZY·April 25, 2013

Siemens Healthcare Diagnostics Inc. MIcroScan MICroSTREP plus Type 1 B1027-201 panels. .MICroSTREP panels are designed for use in determining antimicrobial agent susceptibility of aerobic nonenterococcal streptococci (including Streptococcus pneumoniae) and Haemophilus spp.

FDA Enforcement
Class II ·Terminated·Siemens Healthcare Diagnostics, Inc.·May 15, 2013

Ethicon Stratafix Symmetric PDS Plus Knotless Tissue Control Device Ethicon LLC Guaynabo, Puerto Rico 00969. Intended for general soft tissue approximation where use of an absorbable suture is appropriate.

FDA Recall
Terminated ·Ethicon, Inc. US·Product code NEW·September 25, 2013

REFLECTION(R), MICROSTABLE(R), ACETABULAR LINER, 20o OVERHANG, 28 MM ID, 54-56 OD, QTY: (1), STERILE EO, REF 71742854, Smith & Nephew, Inc. Memphis, TN 38116 USA. Orthopaedic.

FDA Recall
Terminated ·Smith & Nephew Inc·Product code LPH·November 25, 2013

LifeScan brand OneTouch Select Control Solution, Part Number/Model #: 02168902. Testing of Blood Glucose Levels.

FDA Recall
Terminated ·Lifescan Inc·Product code JJX·February 25, 2013

NIPRO SET / SLIMLINE BLOOD TUBING SET for Hemodialysis with Transducer Protectors and Priming Set A disposable bloodline intended to provide extracorporeal access to the patient's blood during Hemodialysis. Compatible for use with Fresenius 2008H, 2008K/K2 and 2008T dialysis machines.

FDA Recall
Terminated ·Nipro Medical Corporation·Product code FJK·March 30, 2015

XiO RTP System. Used to create treatment plans for any cancer patient for whom external beam radiation therapy or brachytherapy has been prescribed.

FDA Recall
Terminated ·Elekta, Inc.·Product code MUJ·November 25, 2013

LifeScan brand OneTouch Ultra Control Solution, Part Numbers/Model Numbers: 01045808, 02141603. Testing of Blood Glucose Levels.

FDA Recall
Terminated ·Lifescan Inc·Product code JJX·February 25, 2013

KY SENSITIVE TM JELLY Personal Lubricant. The product is packaged into 3 oz tubes, which are then packed into a printed carton. Distributed by McNeil-PPC Inc.

FDA Recall
Terminated ·Mc-NEIL-PPC, Inc.·Product code NUC·January 25, 2013

VITROS Anti-HBs Calibrators & VITROS Anti-HBs Reagent Packs

FDA Recall
Terminated ·Ortho-Clinical Diagnostics·Product code LOM·October 25, 2013

KY TINGLING JELLY Personal Lubricant. The product is packaged into 5 oz tubes with the UPC printed on it. Distributed By: McNeil-PPC Inc.

FDA Recall
Terminated ·Mc-NEIL-PPC, Inc.·Product code NUC·January 25, 2013

1) Accolade II 127 Neck Angle Hip Stem, Size # 3 2) Accolade II 127 Neck Angle Hip Stem, Size #5 Howmedica Osteonics Corp. 325 Corporate Drive Mahwah, NJ 07430 USA Telephone # +1 201-831-5000 Stryker France ZAC Satolas Green Pusignan Av de Satolas Green 69881 MEYZIEU Cedex France Intended for cementless application in total or hemiarthroplasty procedures.

FDA Recall
Terminated ·Stryker Howmedica Osteonics Corp.·Product code JDI·October 25, 2013