ATTUNE 1517-00-210Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295054498), received between Jul 20, 2026 and Jul 20, 2026 — classified as 1 injury.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).

5 other recalls cover devices cleared under the same FDA submission (K160700, K241000); 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 18, 2026.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJul 20, 2026Device Dislodged or Dislocated

  IT WAS REPORTED THAT THE PATIENT HAD THESE PRODUCTS IMPLANTED ON (B)(6) 2026. LATER THAT NIGHT IN THE PACU PATIENT SUSTAINED A KNEE DISLOCATION, REASONS UNKNOWN. THERE WAS NO EVENT THAT TRIGGERED IT. ACCORDING TO THE DR. ¿IT JUST SORT OF HAPPENED WITHOUT AN INCIDENT¿. THE DR STATS THAT THE PATIENT HAD A HISTORY OF COMPROMISED SOFT TISSUES OF THE LEFT KNEE. SO THE DR EXPLANTED ALL COMPONENTS AND IMPLANTED A HINGE KNEE REVISION PROSTHESIS. DOI: (B)(6) 2026. DOR: (B)(6) 2026. AFFECTED SIDE: LEFT.

  Patient problems: Joint Dislocation

  MAUDE report 25872528 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K160700, K241000. One submission often covers many models, so check the product and lot details in each record.

• Z-0631-2022 · Jan 5, 2022 · Terminated
  ATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 12MM-intended as a Component in total knee arthroplasty (TKA) revision surgeries Product Number: 154909003
• Z-0632-2022 · Jan 5, 2022 · Terminated
  ATTUNE REVISION DISTAL FEMORAL AUGMENT SZ 6 4MM- Intended as a Component in total knee arthroplasty (TKA) revision surgeries Product Number: 154706001
• Z-2348-2021 · Jul 1, 2021 · Terminated
  ATTUNE REVISION CEMENTED STEM 16X80MM-intended for use in total knee arthroplasty Part Number: 1512-16-080
• Z-1704-2018 · Apr 16, 2018 · Terminated
  ATTUNE Revision CRS Femoral RT SZ 5 Cemented, Catalog No. 150440205, Femoral Revision Implant, Knee
• Z-1703-2018 · Apr 16, 2018 · Terminated
  ATTUNE Revision CRS Femoral LT SZ 5 Cemented, Catalog No. 150440105, Femoral Revision Implant, Knee