DePuy Synthes 11.0mm Reamer Head Recalled for Breakage and Tissue Damage
Synthes (USA) Products LLC is recalling DePuy Synthes 11.0mm Reamer Heads for RIA 2 due to breakage exceeding expected rates, which can cause tissue and bone damage.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 4/5 (Severe).
The hazard poses a serious risk of illness, injury, or structural failure. Stop using the product immediately and contact the manufacturer for a refund or repair.
Our severity reasoning: The recall is classified as FDA Class II and involves reports of significant injury, specifically soft tissue and bone damage, which meets the criteria for a Severe rating.
Plain-English summary
Synthes (USA) Products LLC is recalling the DePuy Synthes 11.0mm Reamer Head for RIA 2, a sterile orthopedic manual surgical instrument. The recall affects 1,275 units distributed in the United States and 445 units distributed outside the United States. The product is identified by Part Code 03.404.018S and UDI 10886982273963.
The recall was initiated because the reamer head breakage rate exceeds the expected occurrence. When the recommended surgical techniques are not followed, this breakage can result in adverse tissue reactions, soft tissue damage, and/or bone damage.
Healthcare providers and facilities that have received this product should stop using it and contact Synthes (USA) Products LLC for further instructions on the recall process.
The recalled product
- Product
- DePuy Synthes 11.0MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual surgical instrument Part Code: 03.404.018S
- 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: 10886982273963
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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