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ATTUNE 2999-65-599Recalls & reported problems

Depuy Orthopaedics, Inc. · ATTUNE MAKE TO ORDER NON-SLOTTED BALANCED ANTERIOR POSTERIOR CUTTING BLOCK SIZE 8 · Class 2

All models of ATTUNE (19)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10603295452751), received between Nov 12, 2021 and Nov 12, 2021 — classified as 1 malfunction.

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

10 other recalls cover devices cleared under the same FDA submission (K140881); 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

Device problems

  • Break1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionNov 12, 2021Break; Break

    IT WAS REPORTED THAT THE LEVER BROKE OFF THE CUTTING BLOCK. NO SURGICAL DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12803767 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K140881. One submission often covers many models, so check the product and lot details in each record.

  • Z-2137-2015 · Jun 12, 2015 · Terminated
    ATTUNE FB PS ARTICULATION SURFACE SIZES 3-8 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the Shim component to function as the Insert Trial during a tot
  • Z-2139-2015 · Jun 12, 2015 · Terminated
    ATTUNE RP PS ARTICULATION SURFACE SIZE 3-8 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the Shim component to function as the Insert Trial during a tota
  • Z-2141-2015 · Jun 12, 2015 · Terminated
    ATTUNE RP CR ARTICULATION SURFACE SIZE 3-8 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the Shim component to function as the Insert Trial during a total
  • Z-2146-2015 · Jun 12, 2015 · Terminated
    ATTUNE CONV FB CR TB TRL SZ3 - 10 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the Shim component to function as the Insert Trial during a total knee re
  • Z-2138-2015 · Jun 12, 2015 · Terminated
    ATTUNE FB CR ARTICULATION SURFACE SIZE 3-8 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the Shim component to function as the Insert Trial during a tota
  • Z-2142-2015 · Jun 12, 2015 · Terminated
    ATTUNE CONV FB PS ARTICULATION SURFACE SZ1-10 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the Shim component to function as the Insert Trial during a t
  • Z-2144-2015 · Jun 12, 2015 · Terminated
    ATTUNE CONV RP PS TB TRL SZ10 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the Shim component to function as the Insert Trial during a total knee repla
  • Z-2143-2015 · Jun 12, 2015 · Terminated
    ATTUNE CONV RP PS ARTICULATION SURFACE SZ1-9 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the Shim component to function as the Insert Trial during a to
  • Z-2145-2015 · Jun 12, 2015 · Terminated
    ATTUNE CONV FB CR ARTICULATION SURFACE SZ1 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the Shim component to function as the Insert Trial during a tot
  • Z-2140-2015 · Jun 12, 2015 · Terminated
    ATTUNE CONV RP CR ARTICULATION SURFACE SZ1, 2, 9, and 10 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the Shim component to function as the Insert Tria

Other PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices

All PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER devices →

Sources and updates

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