PathFinder NXT Pivoting Percutaneous Rod Holder This device is an instrument used during orthopedic surgery. The intended use of the pivoting percutaneous rod holder is to attach to the rod to facilitate rod insertion, positioning, and orientation through the extender sleeves, under the fascia. The rod is secured to the holder by tightening a captive set screw against the rod end in the tip of the holder using the set screw driver. After positioning the rod and securing at least one pedicle screw closure top against the implanted rod, the holder is removed from the rod end by loosening the captive set screw with the set screw driver.
FDA Recall Z-1933-2012 · Posted 2012-07-03
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Recalling FirmZimmer, Inc.
Recall StatusTerminated
Product CodeNKB
Date Initiated2012-06-05
Date Terminated2013-02-14
Product Quantity77 units
Reason for Recall
Complaints have been reported where, during surgery, the surgeon was unable to loosen or
remove the inserted rod from the rod holder instrument. The complaint investigation showed
the hex mating feature of the set screw was broken and material missing. There were no
reports of fragments of the set screw being left in the patient or that there was any patient or
user injury, but these events we
Firm Action
The firm, Zimmer Spine, sent an "URGENT MEDICAL DEVICE RECALL" letter dated June 5, 2012 to all consignees/customers. The letter described the product, problem and actions to be taken. The customers were instructed to review the notification and ensure they are aware of the content; to immediately remove and discontinue use of Pivoting Percutaneous Rod Holder (part number 3564-1) from Pathfinder NXT instrument sets in their possession and follow the PathFinder NXT Surgical Technique; to notify their Zimmer Spine customer service representative to obtain return authorization; and return the complete Surgeon Contact Certification Form within 10 working days from receipt of notification to [email protected] or Fax to 1-512-258-0995.
If you have any questions, call Zimmer Spine Customer Service at 866-774-6368.
Root Cause
Device Design
Distribution Pattern
Worldwide distribution: USA (nationwide) and countries of: Australia, France and Germany.
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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