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Johnson & Johnson's Unit Recalls Bone Putty-Reuters


Tuesday, 21 Aug 2012 02:16pm EDT 

Reuters reported that the U.S. health regulator said certain lots of bone putty made by Johnson & Johnson's unit Synthes were recalled as there was potential for the putty to catch fire if it came in contact with electrosurgical cautery systems during surgery. The Hemostatic Bone Putty is used to stop bone bleeding by creating a physical barrier along the edges of bones damaged by trauma or cut during a surgical procedure. The recall, which has been classified as Class I, or the most serious type of recall, was initiated on July 5. The U.S. health regulator said certain lots of bone putty made by Johnson & Johnson unit Synthes were recalled as there was potential for the putty to catch fire if it came in contact with electrosurgical cautery systems during surgery. The Hemostatic Bone Putty is used to stop bone bleeding by creating a physical barrier along the edges of bones damaged by trauma or cut during a surgical procedure. The recall, which has been classified as Class I, or the most serious type of recall, was initiated on July 5. 

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