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Titan™ Total Shoulder System

Ascension Orthopedics, Inc. · Model GLN092003001K · UDI-DI 10381780120179

KWSHSD Prescription
1
510(k) clearances
23,453
Adverse events (33 deaths)
153
Recalls
216
Facilities

Description

The Titan Modular Total Shoulder System Keeled Glenoid is used in conjunction with metaphyseal bodies, humeral stems, and humeral heads in the TITAN™ Modular Total Shoulder System for total replacement Arthroplasty and provide stable fixation, proximal bone loading, and proper head placement. The glenoid component is intended for use of correction of humeral joint due to severely painful and/or disabled joint resulting from osteoarthritis, traumatic arthritis or rheumatoid arthritis. The component is also used in repairing fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon’s experience indicates that alternative methods of treatment are unsatisfactory as well as other difficult clinical problems where shoulder arthrodesis or resection arthroplasty are not acceptable (e.g. – revision of a failed primary component).

Recalls

DateFirmReason
2026-07-30Howmedica Osteonics Corp.Affected devices were manufactured with Ultra High Molecular Weight Polyethylene (UHMWPE) raw material aged in excess of five years. Product has the potential for elevated levels o
2026-03-05Tornier, IncAffected products were incorrectly labeled as Tornier HRS Max products. These parts are compatible with the Tornier HRS system only, and are incompatible with the Tornier HRS Max s
2026-01-15Encore Medical, LPKnee and Humeral socket implants contain incorrect labeling.
2025-12-19Tornier, IncA specific lot of screws is incorrectly labeled. Screws are labeled as 5.0mmx18mm but actual screws are 5.00mmx14mm. If mismatch is detected during surgery, the issue may cause a m
2025-07-18Encore Medical, LPTheir is a potential that the reamer may kick or bind up during or immediately prior to use.
2025-07-18Encore Medical, LPTheir is a potential that the reamer may kick or bind up during or immediately prior to use.
2025-07-18Encore Medical, LPTheir is a potential that the reamer may kick or bind up during or immediately prior to use.
2024-03-06Exactech, Inc.The packaging of these affected UHMWPE humeral liners and glenoids are nonconforming as they do not meet the established packaging specification. They were packaged in vacuum bags
2024-03-06Exactech, Inc.The packaging of these affected UHMWPE humeral liners and glenoids are nonconforming as they do not meet the established packaging specification. They were packaged in vacuum bags
2024-03-06Exactech, Inc.The packaging of these affected UHMWPE humeral liners and glenoids are nonconforming as they do not meet the established packaging specification. They were packaged in vacuum bags

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.