Adverse-event reports (MAUDE)
Read this first: MAUDE report counts cannot be used to compute incidence rates or compare device safety. Reporting is incomplete, duplicated, and spikes with publicity; there is no denominator of devices in use. The peer line shows reporting volume for the average device in the same FDA product code — a reporting baseline, not a risk measure.
No adverse-event reports are linked to this device.
Recall history
No recalls linked.
Regulatory clearances
None linked.
Manufacturer compliance record
| Date | Type | Outcome | Facility | Citations |
|---|---|---|---|---|
| 2024-03-28 | NAI | No action indicated | DePuy Orthopaedics, Inc. | 0 |
| 2022-05-12 | NAI | No action indicated | DePuy Orthopaedics, Inc. | 0 |
| 2019-11-08 | NAI | No action indicated | DePuy Orthopaedics, Inc. | 0 |
| 2017-09-01 | VAI | Voluntary action indicated | DePuy Orthopaedics, Inc. | 2 |
| 2015-10-01 | VAI | Voluntary action indicated | DePuy Orthopaedics, Inc. | 2 |
| 2015-09-24 | NAI | No action indicated | DePuy Orthopaedics, Inc. | 0 |
| 2012-11-26 | VAI | Voluntary action indicated | DePuy Orthopaedics, Inc. | 6 |
| 2011-12-08 | WL | Warning Letter | DePuy Orthopaedics, Inc. | — |
| 2011-08-16 | NAI | No action indicated | DePuy Orthopaedics, Inc. | 0 |
| 2011-06-07 | OAI | Official action indicated | DePuy Orthopaedics, Inc. | 6 |
| 2010-08-19 | WL | Warning Letter | DePuy Orthopaedics, Inc. | — |
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