DJO SURGICAL 341-16-707Recalls & reported problems
Encore Medical, L.P. · EMPOWR 3D KNEETM INS, 7L 16MM, VE · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00888912167147), received between Apr 25, 2019 and Mar 19, 2026 — classified as 4 injuries.
The most frequently reported specific device problem is “Unstable” (2 reports).
1 FDA recall record name this device's identifier, 1 still open.
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.
Reports received per month
Recalls naming this device
- Jan 15, 2026Class IIOpen, Classified
Knee and Humeral socket implants contain incorrect labeling.
Z-1459-2026 · Root cause: Process control · Recall details · FDA record ↗
Most reported problems
Device problems
- Unstable2
- Adverse Event Without Identified Device or Use Problem1
- Appropriate Device Problem Term/Code Not Available1
- Loosening of Implant Not Related to Bone-Ingrowth1
Patient problems
- Unspecified Infection2
- Joint Dislocation1
- No Known Impact Or Consequence To Patient1
- Unspecified Tissue Injury1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryMar 19, 2026Adverse Event Without Identified Device or Use Problem
InjuryDec 6, 2021Unstable; Loosening of Implant Not Related to Bone-Ingrowth
REVISION SURGERY - THE PATIENT HAD AN ACUTE INJURY CAUSING HIS LEFT KNEE TO DISLOCATE. HE STARTED TO EXPERIENCE LOOSENING AND INSTABILITY.
Patient problems: Joint Dislocation; Unspecified Tissue Injury
MAUDE report 12936958 ↗InjuryMay 2, 2019Unstable
REVISION SURGERY - DUE TO INSTABILITY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8573450 ↗InjuryApr 25, 2019Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO AN INFECTION.
Patient problems: Unspecified Infection
MAUDE report 8552086 ↗
Other Guide, Surgical, Instrument devices
- NA 03.037.017Synthes GmbH · Guide, surgical, instrument346 reports
- EVOS 71174934Smith & Nephew, Inc. · Guide, surgical, instrument149 reports
- LCP 323.042Synthes GmbH · Guide, surgical, instrument129 reports
- DJO SURGICAL 342-10-705Encore Medical, L.P. · Guide, Surgical, Instrument1 recall51 reports
- DJO SURGICAL 341-10-707Encore Medical, L.P. · Guide, Surgical, Instrument81 reports
- NA 03.010.404Synthes GmbH · Guide, surgical, instrument73 reports
- DJO SURGICAL 341-14-708Encore Medical, L.P. · Guide, Surgical, Instrument1 recall22 reports
- DJO SURGICAL 341-10-711Encore Medical, L.P. · Guide, Surgical, Instrument1 recall16 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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