Implant Partners DLXPGD36WDRecalls & reported problems
Microport Orthopedics Inc. · POLY 0DG LINER 36MM GRP D A-CLASS® IMPLANT PARTNERS™ · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI M684DLXPGD36WD1), received between Sep 26, 2024 and Sep 26, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).
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
Most reported problems
Device problems
- Detachment of Device or Device Component1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 26, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
ALLEGEDLY, DISASSOCIATION OF POLY LINER FROM SHELL. REVISION PROCEDURE ENTAILED REMOVING THE FEMORAL HEAD AND DISASSOCIATED POLY LINER. THE SHELL WAS WELL AFFIXED SO THE DR. PROCEEDED WITH INSERTING A DUAL MOBILITY METAL LINER WITH THE APPROPRIATELY SIZED LINER, DUAL MOBILITY INSERT, AND APPROPRIATE CERAMIC 28MM HEAD NON-REVISED PRODUCTS: PRODUCT ID: DBFPGD52 DYNASTY® BF SHELL PRIMARY 52MM GROUP D/ LOT NO.: 1955983/ QTY: 1 PRODUCT ID: PRGLCLS1 PROFEMUR® GLADIATOR® CLASSIC PLASMA SIZE 1 STRAIGHT NECK/ LOT NO.: 1936519/ QTY: 1.
Patient problems: Insufficient Information
MAUDE report 20313870 ↗
Other Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented devices
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- BIOLOX DELTA 1365-32-320Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented1 death314 reports
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- DJO SURGICAL 400-03-362Encore Medical, L.P. · Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented187 reports
- Anthology 71365705Smith & Nephew, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented176 reports
- BIOLOX DELTA 1365-40-710Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented170 reports
- PINNACLE GRIPTION 1217-32-054Depuy Orthopaedics, Inc. · Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented169 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
- 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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