3 results
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18ms
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Sources: EU EUDAMED, US FDA
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FDA Recall
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1757-1: Compressor/Distractor Instrument (aka Plate Distractor Forceps), and product literature. Devices are manufactured by Spinal Concepts, Inc., An Abbott Laboratories Company
FDA Recall
Terminated
·Spinal Concepts, Inc·Product code KWQ·March 1, 2004
One-level Ant-Cer Plates (Assembly Level). 1706-1024, 1706-1026, 1706-1028, 1706-1030, 1706-1032, and product literature. Devices are manufactured by Spinal Concepts, Inc., An Abbott Laboratories Company
FDA Recall
Terminated
·Spinal Concepts, Inc·Product code KWQ·March 1, 2004
Intake/Reservoir Valve (Part No. 875400), used in all sizes of Laerdal Silicone Resuscitators. Responsible firm on the label: Distributed in the U.S. by Laerdal Medical Corporation, Wappingers Falls, NY, Made in Norway.
FDA Recall
Terminated
·Laerdal Medical Corporation·Product code BTM·December 23, 2003