Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hoffman LRF Wire Bolt Recalled by Stryker Howmedica Osteonics Corp. Due to Two complaints have been filed where Hoffman LRF...
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 Stryker Howmedica Osteonics Corp. directly.
Affected Products
Hoffman LRF Wire Bolt, Catalog number 4933-1-001 through -003.
Quantity: 476 units
Why Was This Recalled?
Two complaints have been filed where Hoffman LRF Wires have broken during load bearing application by patients.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker Howmedica Osteonics Corp.
Stryker Howmedica Osteonics Corp. has 87 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report