Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stem Extractor f/Guide Bar Recalled by Synthes, Inc. Due to There is a potential for the connection screw...
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 Synthes, Inc. directly.
Affected Products
Stem Extractor f/Guide Bar, Part number 03.401.072. Instrumentation for extraction and revision of Epoca shoulder implants.
Quantity: 31
Why Was This Recalled?
There is a potential for the connection screw of the stem extractor to break.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Synthes, Inc.
Synthes, Inc. has 43 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report