NA 402.878Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10886982206732), received between Sep 25, 2020 and Jul 17, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “Break” (1 report).

4 other recalls cover devices cleared under the same FDA submission (K050110, K063049, K112583, K962616); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryJul 17, 2023Break; Break

  DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN JAPAN AS FOLLOWS: IT WAS REPORTED THAT ON (B)(6) 2022, THE PATIENT UNDERWENT AN OPEN REDUCTION INTERNAL FIXATION PROCEDURE FOR A DISTAL CLAVICLE FRACTURE. AFTER SURGERY, ON (B)(6) 2023 , THE THREE SCREWS INSERTED AT THE DISTAL HOLES OF THE PLATE WERE FOUND TO BE BROKEN. REMOVAL SURGERY WAS PERFORMED ON (B)(6) 2023 . BONE UNION WAS ACHIEVED, SO THE PLATE AND SCREWS WILL BE REMOVED. THIS REPORT INVOLVES ONE 2.7MM TI CORTEX SCREW SLF-TPNG WITH T8 STARDRIVE RECESS 18MM. THIS IS REPORT 3 OF 3 FOR (B)(4).

  Patient problems: Nonunion/Delayed-union Bone Fracture

  MAUDE report 17332808 ↗
• InjurySep 25, 2020Off-Label Use; Off-Label Use

  DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN (B)(6) AS FOLLOWS: IT WAS REPORTED THAT ON (B)(6) 2020 DURING AN OPEN REDUCTION FIBULA AND TIBIA PROCEDURE, THE SURGEON IMPLANTED LATERAL DISTAL FIBULAR PLATES AND USED 2.7MM CORTICAL SCREWS IN THE BODY OF THE PLATE INSTEAD OF THE INDICATED 3.5MM SCREWS. AFTER A PREVIOUS PROCEDURE, THE SURGEON DIRECTED THE STAFF TO RETAIN 3.5MM SCREWS AND THEY WERE SENT TO BE STERILIZED. THE SURGEON BEGAN THE PATIENT'S PROCEDURE WITHOUT THE 3.5MM BEING AVAILABLE AS THEY WERE STILL BEING STERILIZED. AFTER BEING ADVISED THAT USING THE 2.7MM CORTICAL SCREWS COULD GENERATED COMPLICATIONS IN THE PATIENT, THE SURGEON PROCEEDED TO IMPLANT THE 2.7MM CORTICAL SCREWS. THERE IS NO FURTHER INFORMATION AVAILABLE. THIS REPORT IS FOR ONE (1) 2.7MM TI CORTEX SCREW SLF-TPNG WITH T8 STARDRIVE RECESS 18MM. THIS IS REPORT 4 OF 10 FOR (B)(4).

  Patient problems: Injury; No Code Available

  MAUDE report 10587882 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K050110, K063049, K112583, K962616. One submission often covers many models, so check the product and lot details in each record.

• Z-2389-2016 · Jun 28, 2016 · Terminated
  Synthes 2.4mm Titanium Locking Screws Self-Tapping with Stardrive Recess 12mm, Synthes 2.4mm Titanium Locking Screws Self-Tapping with Stardrive Recess 12mm, Plate, Fixation, Bone,
• Z-0323-2016 · Nov 2, 2015 · Terminated
  2.4MM locking screw SLF-TPNG with Stardrive Recess 18 mm. Intended for fixation of fractures, osteotomies, nonunions, replantations, and fusions of small bones and small bone frag
• Z-0167-2016 · Oct 6, 2015 · Terminated
  2.7 mm Locking Screw SLF-TPNG with T8 Stardrive Recess 12mm. The Synthes modular Mini Fragment LCP System is intended for fixation of fractures, osteotomies, nonunions, replantati
• Z-0380-2014 · Jul 31, 2013 · Terminated
  2.4 and 2.7 MM Locking Screw SLF-TPNG with T8 Stardrive Recess 12 MM Fixation of fractures, osteotomies, nonunions, replantations, and fusions of small bones and small bone fragmen