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Terminated

Reamer / Irrigator / Aspirator (RIA): RIA Drive Shafts, RIA Tube Assemblies, sterile, RIA Reamer Head, sterile (12.0mm-19.0mm); intended to clear the medullary canal of bone marrow and debris and to effectively size the medullary canal for the acceptance of an intramedullary implant or prosthesis

FDA Recall Z-2092-2015 · Posted 2015-07-16

Recalling FirmSynthes, Inc.
Recall StatusTerminated
Product CodeHTO
Date Initiated2015-05-28
Date Terminated2016-08-18
Product Quantity132564

Reason for Recall

It was reported that the RIA Drive Shaft, Tube Assembly, and Reamer Head have the potential to break when incorrectly assembled or used improperly. Precautionary statements are being added to the Reamer / Irrigator / Aspirator (RIA) Surgical Technique Guide.

Firm Action

DePuy Synthes sent an Urgent Medical Device Safety Notification dated May 28, 2015, to direct accounts and sales consultants to advise them of the patient risk associated with misassembly or misuse of the device. Customers and sales force were instructed to remove the Surgical Technique Guide J4352 (all versions) dated 11/2011 or earlier and replace it with the updated Technique Guide (DSUS/TRM/0515/0620, Date 06/2015),and to return the completed verification response form. If you have any further questions, please call (610) 719-5450. Thank you for your attention to this matter.

Root Cause

Labeling False and Misleading

Distribution Pattern

Nationwide Distribution and Internationally to Canada and Switzerland.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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