Povidine iodine prep pads are used to prevent infection in minor cuts, scrapes and burns and are labeled as an antiseptic for preparation of the skin prior to surgery. The prep pads contain some of the same raw material as the recalled alcohol prep pads recently recalled by Triad and were therefore investigated by FDA and H&P for potential contamination. Analytical testing showed the presence of objectionable organisms, namely Elizabethkingia meningoseptica. There have not been any reports of adverse events in connection with the contaminated iodine prep pads.
Read the news release about the recalled povidine iodine prep pads.
Read other coverage about recalls by Triad Group:
– Triad to Shut Down Healthcare Line Following Recalls
– Smith & Nephew Recalls IV Prep Antiseptic Wipes
– Triad Sterile Lubricating Jelly Recalled
At the Becker’s 32nd Annual Meeting: The Business and Operations of ASCs, taking place October 29-31 in Chicago, ASC leaders, surgeons and healthcare executives will explore strategies to drive growth, enhance operational performance, navigate reimbursement challenges and prepare for the future of ambulatory surgery. Apply for complimentary registration now.