Additional H&P Products Recalled

Custom surgical kits, manufactured by H&P Industries, have been recalled due to inadequate microbial testing, according to an FDA news release.

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The kits contained povidone iodine prep solution, which has been the subject of recalls since December 2010. Since then, H&P Industries initiated several product recalls due to bacterial contamination. H&P and distributor Triad Group were placed under consent decree prohibiting the companies from manufacturing and distributing products.

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