Custom surgical kits, manufactured by H&P Industries, have been recalled due to inadequate microbial testing, according to an FDA news release.
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.
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.
More Articles on Quality:
6-Step Strategy for Promoting Patient Safety Innovation
Patient Safety Tool: Personal Protective Equipment Education and Competency Tools
Nearly Dozen Fatal Occupational Injuries in Hospital, Ambulatory Industries in 2011