Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
32MM -4 V40 TAPER VIT HEAD Recalled by Howmedica Osteonics Corp. Due to There is a potential for the outer Tyvek...
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
32MM -4 V40 TAPER VIT HEAD, Catalog Number 6260-5-032
Quantity: 8 units
Why Was This Recalled?
There is a potential for the outer Tyvek lid to de-bond from the sealed package.
Where Was This Sold?
Worldwide distribution - US Puerto Rico and the countries of Canada, and Malaysia.
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