DELTA CUP ACCESSORIES Neutral Liner (REF 5885.51.158)Recalls & reported problems
Limacorporate SPA · Neutral Liners (UHMWPE X-LIMA + Ti6Al4V) 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 08033390041072), received between Dec 4, 2018 and Dec 4, 2018 — 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.
Most reported problems
Device problems
- Device Dislodged or Dislocated1
Patient problems
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 4, 2018Device Dislodged or Dislocated
HIP REVISION SURGERY DUE TO FREQUENT DISLOCATIONS PERFORMED ON (B)(6) 2018. PREVIOUS SURGERY PERFORMED ON (B)(6) 2014. ACCORDING TO THE INFO PROVIDED, THE SURGEON HAD PLANNED TO REPLACE NECK AND LINER TO INCREASE STABILITY, BUT DURING SURGERY HE WAS FORCED TO REMOVE ALSO THE STEM BECAUSE IT WAS NOT POSSIBLE TO DISENGAGE IT FROM THE NECK DUE TO AN INTRA-OP ISSUE INVOLVING THE NECK EXTRACTOR (STEM, NECK AND EXTRACTOR ARE NOT MARKETED IN THE USA). THE EXPLANTED COMPONENTS ARE THE FOLLOWING: - DELTA NEUTR.LINER ØINT 32MM #M CODE 5885.51.158 LOT# 1406267. - MODULUS NECK S TAPER B 12/14 CODE 7590.15.030 LOT# 1403514. - MODULUS MOD.STEM Ø23 MM 4310.15.110 LOT# 1303564. - FEM. MODULAR HEAD - M Ø32MM 5010.42.322 LOT# 1481197. COMPONENTS FROM ANOTHER MANUFACTURER HAVE THEN BEEN IMPLANTED. EVENT HAPPENED IN JAPAN.
Patient problems: No Code Available
MAUDE report 8127812 ↗
Other Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Porous devices
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- 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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