Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ReClaim Reamer Extension Recalled by DePuy Orthopaedics, Inc. Due to The tabs on the reamer extension device have...
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 DePuy Orthopaedics, Inc. directly.
Affected Products
ReClaim Reamer Extension; Product code 2975-00-500, used with Reclaim Modular Revision Hip Prosthesis System. The ReClaim Reamer Extension is as an attachment to the distal reamers to allow the surgeon to clear soft tissue while reaming the distal femoral canal.
Quantity: 750
Why Was This Recalled?
The tabs on the reamer extension device have broken. DePuy is notifying surgeons of the issue to increase the awareness and to ask surgeons and users to look for tabs before and after surgery to reduce any potential that the tabs are left in the patient. Once the root cause is determined and a design change is implemented, DePuy will conduct a formal swap-out of the affected devices.
Where Was This Sold?
This product was distributed to 27 states: AZ, AR, CA, CO, FL, GA, HI, IL, IA, KY, LA, ME, MD, MA, MI, MN, MT, NV, NY, NC, OH, PA, TN, TX, VA, WA, WI
About DePuy Orthopaedics, Inc.
DePuy Orthopaedics, Inc. has 154 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report