LPS 2987-40-040Recalls & reported problems
Depuy (Ireland) · LPS IMPLANT TO TRIAL ADAPTER 40mm · Class 1
All models of LPS (113)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10603295158752), received between Jan 17, 2019 and Aug 12, 2025 — classified as 2 malfunctions.
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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
- Device-Device Incompatibility1
- No Apparent Adverse Event1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 12, 2025Detachment of Device or Device Component; No Apparent Adverse Event; Detachment of Device or Device Component; No Apparent Adverse Event
IT WAS REPORTED THAT WHILE OVERLOOKING INSTRUMENTS BEFORE ENTERING FACILITY SPD PROCESS, IT WAS NOTICED THAT THREE SEGMENTAL COMPONENT TRIALS DO NOT MATCH THE OTHER TRIALS IN THE SET. THE THREE AFFECTED SEEM TO BE DIFFERENT BECAUSE THE SEGMENTS DO NOT HAVE A LOCKING RING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22781608 ↗MalfunctionJan 17, 2019Device-Device Incompatibility; Device-Device Incompatibility
IT WAS REPORTED THAT THE 40MM TRIAL TO REAL IMPLANT SEGMENT IS NOT ATTACHING CORRECTLY. THE TRIAL SITS 10-15MM PROUD.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8256744 ↗
Other TEMPLATE devices
- ATTUNE 2544-01-014Depuy (Ireland) · TEMPLATE802 reports
- ATTUNE 2545-00-546Depuy (Ireland) · TEMPLATE1 recall301 reports
- ARTICUL/EZE 2531-51-000Depuy (Ireland) · TEMPLATE323 reports
- DELTA XTEND 2307-95-000Depuy (Ireland) · TEMPLATE315 reports
- ATTUNE 2545-00-547Depuy (Ireland) · TEMPLATE1 recall231 reports
- ATTUNE 2544-00-520Depuy (Ireland) · TEMPLATE279 reports
- ARTICUL/EZE 2530-91-000Depuy (Ireland) · TEMPLATE271 reports
- ATTUNE 2545-00-545Depuy (Ireland) · TEMPLATE1 recall221 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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