3 results
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46ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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Code Alert Advanced 4-Way Care Solution, CA520 System, PN 9600-1600, RF Technologies. This product is used to alert caregivers when a patient at risk for falls is leaving a bed or chair.
FDA Recall
Terminated
·RF Technologies, Inc.·Product code KMI·May 17, 2013
Bed/chair alarm
FDA Recall
Terminated
·RF Technologies, Inc.·Product code KMI·December 16, 2002
Aquamantys 2.3 Bipolar Sealer Model #23-113-1. Product Usage: The Aquamantys Bipolar Sealer is a sterile, bipolar electrosurgical device intended to be used in conjunction with the Aquamantys Pump Generator for delivery of RF energy and saline for hemostatic sealing and coagulation of soft tissue and bone at the operative site. It is intended for, but not limited to orthopaedic, spine, thoracic, and open abdominal surgery. The device is not intended for contraceptive tubal coagulation (permanent female sterilization
FDA Recall
Terminated
·Salient Surgical Technologies, Inc·July 18, 2011