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Andover Healthcare Inc. recalls Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary wound dressing or compression wrap
Recalled October 30, 2019 · FDA recall Z-0182-2020 · Andover Healthcare
Hazard
Incomplete packaging seal of sterile product · FDA Class II
Units
1759 Cases
Sold at
US Nationwide distribution including the states of MA, TX, RI, OH, NY, MN, SD, IL, MO, FL, VA, NE, UT, CA
Description
Incomplete packaging seal of sterile product
Product
Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary wound dressing or compression wrap
Manufacturer(s)
Andover Healthcare Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →