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Terminated

Exprt Precision System: Revision Hip, Proximal Body with Bolt, Lateral Offset, Sterile R, djo surgical, REF: 495-00-065, 495-00-075, 495-00-085, 495-01-065, 495-01-075, 495-01-085

FDA Recall Z-1123-2019 · Posted None

Recalling FirmEncore Medical, Lp
Recall StatusTerminated
Product CodeKWZ
Date Initiated2018-09-21
Date Terminated2020-09-16
Product Quantity22

Reason for Recall

Complaints regarding loose proximal body bolts or bolts that were found through x-ray as sitting above the proximal body and not properly seated. Patient risks may include: pain, dissociation, and possible revision surgery

Firm Action

On 09/21/18, Urgent Field Safety Notices, updated surgical techniques, and Acknowledgement and Receipt Forms were emailed to Surgical Sales Agents. The Surgical Technique provides instructions on use of the manual T-handle as the primary tightening method. It also provides instructions for use of the torque wrench to ensure that the readout for the torque wrench is at "0" before torque is applied. Sales agents were asked to affirm that they have read and understood the updated Surgical Technique information provided in the Field Safety Notice Bulletin. They were also asked to affirm that they disseminated this information to all employed and contracted sales reps in their organization. On 01/29/19, Urgent Field Safety Notices were emailed to Surgical Agents. This notice communicated the exchange process for physical product in inventory. The firm will notify Surgical Agents to make arrangements for the exchange of affected inventory with proximal bodies that are packaged with new capture bolts containing a polyethene plug. Surgical Agents with additional questions were encouraged to call 512-834-6255.

Root Cause

Other

Distribution Pattern

US: TN, MN, TX, CO, IL, IN, OH, SC, MS, MI, RI, PA, ME, NY, WA, MO, AR, OK, LA, AL, FL, GA, UT, AZ, CA, NV,.

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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