Home / Recalls / Medical Devices
Cardinal Health 200, LLC recalls KIT, PRE OP DRAH - Product Usage: Preoperative kit used to decolonize intranasal S. aureus.
Recalled October 7, 2020 · FDA recall Z-3016-2020 · Cardinal Health 200
Hazard
Only providing one nasal swab in our pre-operative kit instead of the 4 required for proper treatment. · FDA Class II
Units
9,150 kits
Sold at
US Nationwide distribution including the state of North Carolina.
Description
Only providing one nasal swab in our pre-operative kit instead of the 4 required for proper treatment.
Product
KIT, PRE OP DRAH - Product Usage: Preoperative kit used to decolonize intranasal S. aureus.
Manufacturer(s)
Cardinal Health 200, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →