55 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Terminated
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Welch Allyn AED 10 automated external defibrillator and MRL Jumpstart (collectively "AED 10")
FDA Recall
Terminated
·Welch Allyn Protocol, Inc·Product code MKJ·December 15, 2008
Leksell Gamma Knife C
FDA Recall
Terminated
·Elekta, Inc.·Product code IWB·August 1, 2006
Custom Kit, REF: K05-00843, Revision L, Sterile, Merit Medical Systems, Inc., South Jordan, Utah 84095.
FDA Recall
Terminated
·Merit Medical Systems, Inc.·Product code DQO·April 15, 2008
Custom Kit, Custom Angiographic Kit, REF: K05-YS1032, Revision A, Sterile, Merit Medical Systems, Inc., South Jordan, Utah 84095.
FDA Recall
Terminated
·Merit Medical Systems, Inc.·Product code DQO·April 15, 2008
Custom Kit, Custom Angiographic Kit, REF: K05-YS1025, Sterile, Merit Medical Systems, Inc., South Jordan, Utah 84095.
FDA Recall
Terminated
·Merit Medical Systems, Inc.·Product code DQO·April 15, 2008
OEC 9900 Elite Image-intensified fluoroscopic x-ray system (includes OEC 9900 Elite Fluoroscopy System and 9900 EliteMD Motorized C-arm System), GE Healthcare, Surgery, Salt Lake City, UT.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·April 15, 2008
OEC 9800 Image Intensified fluoroscopic x-ray system (includes OEC 9800, OEC FluoroTrak 9800 Plus, OEC 9800 Plus, and OEC 9800MD Motorized C-arm System), GE Healthcare, Surgery, Salt Lake City, UT.
FDA Recall
Terminated
·OEC Medical Systems, Inc·Product code JAA·April 15, 2008
Depuy DELTA Xtend, Standard humeral PE Cup Dia 38/+3 STD, sterile, Depuy France; REF 130738203. The device is used as a shoulder implant.
FDA Recall
Terminated
·Depuy Orthopaedics, Inc.·Product code KWS·July 10, 2008
Custom Waste Management Kit, K10-01756/B, Sterile EO, Merit Medical Systems, Inc., South Jordan, Utah 84095
FDA Recall
Terminated
·Merit Medical Systems, Inc.·Product code DQO·September 12, 2008
Depuy DELTA Xtend, Standard Humeral PE Cup, Dia 42/+3 STD, sterile, Depuy France; REF 130742203. The device is used as a shoulder implant.
FDA Recall
Terminated
·Depuy Orthopaedics, Inc.·Product code KWS·July 10, 2008
Depuy DELTA Xtend, Standard Humeral PE Cup, Dia 38/+6R RET, sterile, Depuy France; REF 130738106. The device is used as a shoulder implant.
FDA Recall
Terminated
·Depuy Orthopaedics, Inc.·Product code KWS·July 10, 2008
Depuy DELTA Xtend, Standard Humeral PE Cup, Dia 38/+9 STD, sterile, Depuy France; REF 130738209. The device is used as a shoulder implant.
FDA Recall
Terminated
·Depuy Orthopaedics, Inc.·Product code KWS·July 10, 2008
Depuy DELTA Xtend, Standard Humeral PE Cup, Dia 42/+6 STD, sterile, Depuy France; REF 130742206. The device is used as a shoulder implant.
FDA Recall
Terminated
·Depuy Orthopaedics, Inc.·Product code KWS·July 10, 2008
Depuy DELTA Xtend, Standard Humerus PE Cup, Dia 38/+6 STD, sterile, Depuy France; REF 130738206. The device is used as a shoulder implant.
FDA Recall
Terminated
·Depuy Orthopaedics, Inc.·Product code KWS·July 10, 2008
Depuy DELTA Xtend, Standard Humeral PE Cup, Dia 42/+9 STD, sterile, Depuy France; REF 130742209. The device is used as a shoulder implant.
FDA Recall
Terminated
·Depuy Orthopaedics, Inc.·Product code KWS·July 10, 2008
Depuy DELTA Xtend, Standard Humeral PE Cup, Dia 42+6R RET, sterile, Depuy France; REF 130742106. The device is used as a shoulder implant.
FDA Recall
Terminated
·Depuy Orthopaedics, Inc.·Product code KWS·July 10, 2008
Radiation therapy system - Coherence Therapist System 2.1 equipped with Coherence Therapist RTT2.1 or Primeview 3i R2.1, part number 8147667. Medical charged particle Radiation therapy system, part of the firm's beam limiting device/accessory. The product provides data processing, and the SYNGO standard medical imaging platform to provide comprehensive oncology workflow solutions for radiation therapy.
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IYE·May 15, 2008
Radiation therapy system - AG Therapist 3rd party V&R equipped with Coherence Therapist RTT2.1 or Primeview 3i R2.1, part number 7345411. Medical charged particle Radiation therapy system, part of the firm's beam limiting device/accessory. The product provides data processing, and the SYNGO standard medical imaging platform to provide comprehensive oncology workflow solutions for radiation therapy.
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IYE·May 15, 2008
Radiation therapy system - Impression Therapist 3rd party V&R equipped with Coherence Therapist RTT2.1 or Primeview 3i R2.1, part number 7345429. Medical charged particle Radiation therapy system, part of the firm's beam limiting device/accessory. The product provides data processing, and the SYNGO standard medical imaging platform to provide comprehensive oncology workflow solutions for radiation therapy.
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IYE·May 15, 2008
Radiation therapy system - Coherence Impression Therapist System equipped with a Coherence Therapist RTT2.1 or Primeview 3i R2.1 part number 7341410. Medical charged particle Radiation therapy system, part of the firm's beam limiting device/accessory. The product provides data processing, and the SYNGO standard medical imaging platform to provide comprehensive oncology workflow solutions for radiation therapy.
FDA Recall
Terminated
·Siemens Medical Solutions USA, Inc·Product code IYE·May 15, 2008