DELTA LINERS & ACCESSORIES 5885.54.157Recalls & reported problems
Limacorporate SPA · Neutral LimaVit Liner I.D. 32mm, size MEDIUM- · 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 08033390136099), received between May 26, 2026 and May 26, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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
- Device Dislodged or Dislocated1
Patient problems
- Joint Dislocation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 26, 2026Device Dislodged or Dislocated
REVISION SURGERY WAS PERFORMED ON (B)(6) 2026. PATIENT WAS DISLOCATING THE HIP ANTERIOR. PREVIOUS SURGERY OCCURRED ON (B)(6) 2026, WHEN DELTA TT PRO ACETABULAR CUP DIA48MM (PN 5553.14.482, LOT 2202752, STERILIZAZTION 2200083) AND DELTA NEUTRAL LINER MEDIUM (PN 5885.54.157, LOT 25AT28X, STERILIZATION 2500129) WERE IMPLANTED IN COMBINATION WITH UNKNOWN FMEORAL COMPONENTS. SINCE PATIENT WAS DISLOCATING THE HIP, THE ABOVE MENTIONED ACETABULAR CUP AND LINER WERE REMOVED AND REPLACED WITH AN ACETABULAR ASSEMBLY CONSISTING OF: DELTA TT ACETABULAR CUP DIA50MM (PN 5552.15.500), DELTA DUAL MOBILITY LINER MEDION FOR MOBILE LINER DIA40 (PN 5885.09.040), DELTA MOBILE LINER (PN 5566.50.401). SURGERY WAS COMPLETED AS INTENDED. PATIENT IS FEMALE, DATE OF BIRTH (B)(6) 1947. THE EVENT OCCURRED IN THE UNITED STATES.
Patient problems: Joint Dislocation
MAUDE report 25278191 ↗
Other Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous devices
- Accolade 6021-0537Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous46 reports
- PROFEMUR® PHAC1252Microport Orthopedics Inc. · Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous37 reports
- Accolade 6020-0335Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous35 reports
- OXINIUM 71342340Smith & Nephew, Inc. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous32 reports
- EXETER 0580-1-351Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous29 reports
- INSTRUMENT 2101-0200Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous27 reports
- REFLECTION 71330001Smith & Nephew, Inc. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous20 reports
- Accolade 6720-0330Howmedica Osteonics Corp. · Prosthesis, hip, semi-constrained, uncemented, metal/polymer, porous18 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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