The Recall Desk
SevereFDA (Devices)·Z-0587-2021·Announced 2020-12-23

DePuy Synthes 18.0mm Reamer Head Recalled for Breakage and Tissue Damage

Synthes (USA) Products LLC is recalling DePuy Synthes 18.0mm Reamer Heads for RIA 2 due to breakage exceeding expected rates, which can cause tissue and 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 recall is classified as FDA Class II and involves a structural defect (breakage) that results in reported adverse tissue reactions, soft tissue damage, and bone damage, meeting the criteria for a Severe rating.

Plain-English summary

Synthes (USA) Products LLC is recalling DePuy Synthes 18.0mm Reamer Heads for RIA 2, sterile orthopedic manual surgical instruments. The recall affects 542 units in the United States and 154 units outside the United States. The product is identified by Part Code 03.404.032S and UDI 10886982274090.

The recall is issued 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.

The affected products were distributed nationwide in the United States and in several foreign countries, including the United Arab Emirates, Austria, Australia, Belgium, Switzerland, China, Czech Republic, Germany, Spain, United Kingdom, Ireland, Israel, Italy, and Singapore. Healthcare providers and facilities should stop using the affected reamer heads and contact the recalling firm for instructions on return or replacement.

The recalled product

Product
DePuy Synthes 18.0MM REAMER HEAD FOR RIA 2 STERILE-Orthopedic manual surgical instrument Part Code: 03.404.032S
Manufacturer
Synthes (USA) Products LLC
Category
Medical Device — Orthopedic Surgical Instrument
Hazard

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: 10886982274090

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.

See all 17 products in this recall →

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