TT MB Peg TT GlenoidRecalls & reported problems
Limacorporate SPA · SMR TT Metal Back Peg (Ti6Al4V) - S-R Long · Class 2 · Implant
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 08033390084406), received between Nov 24, 2021 and Nov 24, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Break1
- Detachment of Device or Device Component1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 24, 2021Break; Detachment of Device or Device Component; Detachment of Device or Device Component
INTRA-OPERATIVE ISSUE OCCURRED DURING A SHOULDER REVISION SURGERY ON (B)(6) 2021: WHEN TRYING TO SEPARATE THE GLENOSPHERE (SMR GLENOSPHERE Ø36MM SMALL-R CODE 137409105 LOT 1514727) FROM THE BASEPLATE (MR GLENOID BASEPLATE SMALL-R CODE 137515650 LOT 1512389) THE BASEPLATE DISASSEMBLED FROM THE PEG (SMR GLENOID PEG TT SMALL-R #L CODE 137514653 LOT 1513804). DUE TO THIS ISSUE, THE SURGEON HAD TO CONVERT TO HEMI PROSTHESIS AND THE SURGERY TIME WAS PROLONGED OF 10 MINUTES. THIS INCIDENT OCCURRED IN (B)(6). NOTE: THE PRODUCT CODE OF THE BASEPLATE INVOLVED IS NOT MARKETED IN USA.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 12868975 ↗
Other Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented devices
- Equinoxe 320-38-00Exactech, Inc. · Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented3 recalls107 reports
- Equinoxe 320-42-00Exactech, Inc. · Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented3 recalls107 reports
- Equinoxe 320-42-03Exactech, Inc. · Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented2 recalls87 reports
- Equinoxe 320-38-03Exactech, Inc. · Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented2 recalls43 reports
- Equinoxe 320-42-13Exactech, Inc. · Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented2 recalls41 reports
- Equinoxe 320-10-00Exactech, Inc. · Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented132 reports
- Equinoxe 320-36-00Exactech, Inc. · Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented2 recalls27 reports
- Equinoxe 320-42-10Exactech, Inc. · Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented2 recalls14 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.