Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
RECLAIM Distal Reamer Extension Non Sterile REF 2975-00-500 Intended as Recalled by DePuy Orthopaedics, Inc. Due to Specific lots are being recalled due to the...
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 Distal Reamer Extension Non Sterile REF 2975-00-500 Intended as an attachment device to the distal reamers to allow the surgeon to clear soft tissue while reaming the distal femoral canal.
Quantity: 875 units
Why Was This Recalled?
Specific lots are being recalled due to the potential for the tabs to break, leaving fragments in the patient.
Where Was This Sold?
This product was distributed to 27 states: AZ, CA, CO, FL, GA, HI, IL, IN, 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