Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary Recalled by Andover Healthcare Inc. Due to Incomplete packaging seal of sterile product
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Andover Healthcare Inc. directly.
Affected Products
Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary wound dressing or compression wrap
Quantity: 1759 Cases
Why Was This Recalled?
Incomplete packaging seal of sterile product
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Andover Healthcare Inc.
Andover Healthcare Inc. has 7 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report