Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
28MM -4 LFIT V40 HEAD Recalled by Howmedica Osteonics Corp. Due to There is a potential for the outer white...
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 Howmedica Osteonics Corp. directly.
Affected Products
28MM -4 LFIT V40 HEAD, Catalog Number 6260-9-122
Why Was This Recalled?
There is a potential for the outer white Tyvek lid to debond from the sealed package.
Where Was This Sold?
Puerto Rico
About Howmedica Osteonics Corp.
Howmedica Osteonics Corp. has 229 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report