Andover Healthcare Inc. recalls Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary
Recalled Product
Sterile Co-Flex LF2 3" - Product Usage: Single Use secondary wound dressing or compression wrap
Hazard / Issue
Incomplete packaging seal of sterile product
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Manufacturer's product or Catalog # 9300S Expiration Date: 01OCT2021-14JUN2022 LOT # CIOZJV, CI02SW, CI18YA, CI1FJ2
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