Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DT Medical -Hintermann Series H3 Poly Inlay Recalled by DT MedTech, LLC Due to Incorrect package labeling identifying the device
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 DT MedTech, LLC directly.
Affected Products
DT Medical -Hintermann Series H3 Poly Inlay, Size 3 5mm Part Number: 300305 components are prostheses for a mobile bearing ankle joint.
Quantity: 54 units
Why Was This Recalled?
Incorrect package labeling identifying the device
Where Was This Sold?
Australia, Ireland, Korea, Germany
About DT MedTech, LLC
DT MedTech, LLC has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report