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Comprehensive Reverse Shoulder 115331Recalls & reported problems

Biomet Orthopedics, LLC · Class 2 · Implant

All models of Comprehensive Reverse Shoulder (57)

Data updated Oct 16, 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 00880304554283), received between Sep 15, 2026 and Sep 15, 2026 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).

24 other recalls cover devices cleared under the same FDA submission (K080642, K120121, K193373, K992367); they may or may not involve this specific model.

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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 1 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

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 15, 2026Detachment of Device or Device Component

    It was reported that following an initial reverse total shoulder arthroplasty, radiography performed after the procedure showed that the glenosphere had become dislodged/detached. The incision was reopened, and reinsertion of the glenosphere was attempted. The taper did not fit, and the central screw was retightened. The procedure was completed with a replacement taper adapter and a replacement glenosphere. Attempts have been made, and no further information has been provided.

    Patient problems: Insufficient Information

    MAUDE report 50769828 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K080642, K120121, K193373, K992367. One submission often covers many models, so check the product and lot details in each record.

  • Z-0619-2021 · Nov 25, 2020 · Terminated
    Comprehensive Reverse Shoulder System, Item numbers 115394, 115395, 115396, 115398, 180550, 180551, 180552, 180553, 180554, 180555, 180556, 180557, 180558, 180559, 180560, 1805
  • Z-0093-2021 · Sep 2, 2020 · Terminated
    Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate with Taper Adapter-Shoulder Prosthesis item: 010000589 - Product Usage: intended to serve as the foundation for t
  • Z-2144-2020 · Apr 17, 2020 · Terminated
    Extremities Item Number: 1)113954 Hybrid Glenoid Glenoid Base, 4 MM 2) XL-115366 Comprehensive Reverse Shoulder Humeral Bearing, ArComXL, 44 MM X 41 MM, Standard 3) XL-115364 Comp
  • Z-1750-2020 · Mar 13, 2020 · Terminated
    Comprehensive Humeral Tray Taper Extraction Pliers - Replacement Tips, Model Number 110028522 - Product Usage: Intended to be used in surgery to relieve pain and to replace the gle
  • Z-1615-2020 · Feb 25, 2020 · Terminated
    Biomet Comprehensive Reverse Shoulder Glenosphere Mini Baseplate With Taper Adapter-indicated for primary, fracture, or revision total shoulder replacement for the relief of pain a
  • Z-0528-2020 · Aug 21, 2019 · Terminated
    HA Pins (DFS HA Cort Screw), Hoffman/Colles Pins (Colles CSER Sterile w/ Pin Kit) Item Nos: HAA60-09030 HAA60-09040 HAA60-10030 HAA60-10040 HAA60-11030 HAA60-11040 HAA60-11050 HAA
  • Z-0972-2019 · Dec 21, 2018 · Terminated
    Comprehensive Reverse Shoulder System Glenosphere Mini Baseplate with Taper Adapter, Model Number 010000589 Biomet Comprehensive Reverse Shoulder products are indicated for use i
  • Z-1859-2017 · Feb 17, 2017 · Terminated
    various polyethylene implants Extremities, Shoulders and Elbows BioModular Shoulder System; Comprehensive Shoulder System; Comprehensive Reverse Shoulder System Product Usage: Sh
  • Z-1103-2017 · Dec 20, 2016 · Terminated
    Comprehensive Reverse Shoulder System Humeral Tray Model 115340
  • Z-1823-2016 · Apr 1, 2016 · Terminated
    Various trauma and sports medicine instruments and implants. Screw, fixation, bone.
  • Z-1208-2015 · Jan 7, 2015 · Terminated
    Comprehensive Reverse Shoulder Glenosphere Mini Baseplate 25mm with Taper Adaptor, Part Number: 010000589 Lot: 527400
  • Z-1548-2013 · May 15, 2013 · Terminated
    Superior Approach Resection Guide Assembly. Indicated for primary, fracture, or revision total shoulder replacement for the relief of pain.
  • Z-2547-2011 · Apr 22, 2011 · Terminated
    Custom solar comprehensive reverse humeral tray with lock ring 44 mm +5mm, sterile, REF CP561659, Biomet Orthopedics, Warsaw, IN. Biomet Comprehensive Reverse Shoulder product
  • Z-2542-2011 · Apr 22, 2011 · Terminated
    Bio-modular reverse shoulder humeral tray with lock ring, 44 mm standard, sterile, single use, REF 11-113680, Biomet Orthopedics, Warsaw, IN. Biomet Comprehensive Reverse Shoulder
  • Z-2550-2011 · Apr 22, 2011 · Terminated
    Custom comprehensive reverse shoulder bio-modular base 44 mm humeral tray standard, REF CP561510, Biomet Orthopedics, Warsaw, IN. Biomet Comprehensive Reverse Shoulder product

…and 9 more.

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Sources and updates

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