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: Bodily Injury BlogJohnson & Johnson Recalls Wound Sealant
By Edward Bills
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The Ethicon unit of Johnson and Johnson (J&J) has announced a recall of 700,000 vials of a liquid wound sealant and also a hernia-treatment product. The Dermabond adhesive was recalled due to discoloration, the company reported, and Securestrap product, used in hernia repair, was pulled because its packaging might not be sterile. |
Full post as published by Bodily Injury Blog on February 22, 2011 (boomark / email).
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