DePuy Synthes 10.0MM Reamer Head Recalled for Breakage and Tissue Damage
Synthes (USA) Products LLC is recalling DePuy Synthes 10.0MM Reamer Heads for RIA 2 because breakage exceeds expected rates, causing potential tissue or bone damage.
What this means for you
Illness, injury, or structural failure has been reported. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The source text explicitly reports adverse tissue reactions, soft tissue damage, and bone damage, which aligns with the rubric criterion for 'significant injury' reports under a Class II recall.
Plain-English summary
Synthes (USA) Products LLC is recalling the DePuy Synthes 10.0MM Reamer Head for RIA 2, a sterile orthopedic manual surgical instrument. The recall involves 1,297 units distributed in the United States and 528 units distributed outside the United States. The product is identified by Part Code 03.404.016S and UDI 10886982273932.
The recall is being conducted because the reamer head breakage rate exceeds the expected occurrence. This breakage can result in adverse tissue reactions, soft tissue damage, and/or bone damage when recommended surgical techniques are not followed. The agency has classified this as a Class II recall.
Healthcare providers and facilities that have received this product should stop using it and contact Synthes (USA) Products LLC for instructions on return or replacement. Consumers are not directly affected as this is a professional medical device.
The recalled product
- Product
- DePuy Synthes 10.0MM REAMER HEAD FOR RIA 2, STERILE-Orthopedic manual surgical instrument Part Code: 03.404.016S
- Manufacturer
- Synthes (USA) Products LLC
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- All Lots UDI: 10886982273932
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 17 recalled by Synthes (USA) Products LLC under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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