2 results
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21ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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Liko Mobile Lifts: Primarily intended for use in nursing homes Liko M220, Model 2050010
FDA Recall
Open, Classified
·Hill-Rom, Inc.·Product code FSA·December 23, 2021
iLink Bone Void Filler. Packaged in a double Tyvek pouch, then placed in a box. Model Number: 50-05-0010, Exp. 2010-04.
FDA Recall
Terminated
·Theken Spine LLC·Product code MQV·August 26, 2008