GLENWOOD SPRINGS — A rare bacterial infection contracted at a Denver-area hospital by a Glenwood Springs boy who is battling leukemia prompted a national recall of tainted alcohol wipes.
The surgical prep pads, swabs and wipes manufactured by the Triad Group of Hartland, Wis., are suspected of being contaminated with a potentially deadly bacteria. The product was voluntarily recalled by the company on Jan. 5 following an investigation by the Food and Drug Administration.
Months later, the boy’s mother, Jessica Armstrong, remains on a mission to make sure what happened to her son does not happen to others.
The Triad products were widely used in medical facilities around the country and were available for sale to consumers under a variety of product names at Safeway, City Market and Walgreens stores.
“Anyone who has or thinks they may have these prep pads or wipes in their home needs to check to confirm the manufacturer, and discard them in the trash immediately,” Armstrong said.
Her family’s ordeal received national media attention with a report on MSNBC. That report referred to several infection cases around the country blamed on the Triad wipes, including one involving the death of 2-year-old boy in Texas in early December 2010.
Jessica and husband Noel Armstrong’s story began when their 10-year-old son, Peyton, was airlifted to Children’s Hospital in Aurora on Oct. 18, 2010, after he had been extremely sick for several weeks.
At Children’s, he was diagnosed with a type of leukemia that required quick action. Peyton had surgery to insert an internal catheter so he could immediately begin chemotherapy treatment.
“Within 12 hours of the surgery, in the middle of the night, he started having this excruciating pain,” his mother said.
Soon, the pain was accompanied by a fever, indicating that Peyton had contracted an infection. Infectious disease experts were called in, and the cause of the infection was narrowed down to the Bacillus cereus bacteria.
Peyton was put on strong antibiotics to stabilize his condition and had to undergo another emergency surgery, followed by a stay in the intensive care unit, she said.
Because of concerns about Peyton’s case and a series of similar infections involving other young patients, Children’s Hospital officials contacted the FDA. In late November, Children’s confirmed that the source of the bacteria was the surgical prep pads.
With the new information, Triad voluntarily issued the product recall.
“Peyton’s case was the catalyst for breaking this investigation, because his surgical site was infected,” Jessica Armstrong said.
“It was very telling, because it was different than a bloodstream infection. I really want to praise Children’s for being so diligent and doing the extensive research to find out the cause.”
But she’s still worried, even after hundreds of thousands of letters went out to medical facilities and retailers, that the tainted wipes may still be lingering in home medicine cabinets or medical kits.
Armstrong said her son is “faring OK” now, despite the ongoing chemotherapy treatments that will last three years.
