Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Orthopedic manual surgical instrument Usage: Exeter Rasp Handle is a Recalled by Stryker Howmedica Osteonics Corp. Due to Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle.
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
Orthopedic manual surgical instrument Usage: Exeter Rasp Handle is a reusable instrument which is part of the Exeter femoral hip system. Exeter femoral rasps are assembled with the rasp handle and locked in place by closing down the lever on the rasp handle. The rasp handle is then used to guide the rasp into the patients femur and is impacted using a mallet in order to remove bone and further prepare the femur.
Quantity: 241 units
Why Was This Recalled?
Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle.
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