Atar Extension Cables Recalled
The recall by Oscor Inc. of its Atar extension cables. On July 6, the U.S. Food and Drug Administration (FDA) announced the recall by Oscor Inc. of its Atar extension cables. The Florida-based device maker issued the recall on March 27, 2017 and was initiated due to a concern that during use, some of the cables were separating from … [Read more...] about Atar Extension Cables Recalled
DePuy LCS Complete RPS Knee System Recall
DePuy Orthopaedics issued a recall for the LCS Complete RPS Knee System. On May 26, DePuy Orthopaedics issued a recall for the LCS Complete RPS Knee System after Australia's Therapeutic Goods Administration reported higher rates of revision (corrective surgery) when the native patella is not resurfaced during the original … [Read more...] about DePuy LCS Complete RPS Knee System Recall
Medtronic SynchroMed and IsoMed Infusion Systems Recall
Infusion systems has now been deemed a Class I recall. Medtronic Inc.'s January communication regarding problems with its SynchroMed and IsoMed infusion systems has now been deemed a Class I recall by the Food & Drug Administration (FDA). A Class I recall indicates a situation in which there is a reasonable probability that use … [Read more...] about Medtronic SynchroMed and IsoMed Infusion Systems Recall
