medical Class II Updated 2019-10-30

Andover Healthcare Inc. recalls Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary

Recalled Product

Sterile Co-Flex LF2 4" - 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 # 9400S Expiration Date: 01OCT2021-14JUN2022 Lot # CI147V, CI15F1, CI17B9, CI18Y0, CI1FJ3, CI1JCF
View official government recall

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