Equinoxe 310-01-44 (UDI 10885862657572)Recalls & reported problems
Exactech, Inc. · Humeral Head, Short · Class 2 · Implant
All models of Equinoxe (305)
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 10885862657572), received between Jun 8, 2026 and Jun 8, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Naturally Worn” (1 report).
10 other recalls cover devices cleared under the same FDA submission (K042021); 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
Most reported problems
Device problems
- Naturally Worn1
Patient problems
- Metal Related Pathology1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 8, 2026Naturally Worn
IT WAS REPORTED THAT THIS PATIENT UNDERWENT A LEFT SHOULDER REPLACEMENT. SUBSEQUENTLY, THEY HAD A REVISION SURGERY FOR PAIN AND DECREASED FUNCTION. INTRAOPERATIVE FINDINGS DEMONSTRATED EXTENSIVE POLYETHYLENE WEAR OF THE GLENOID COMPONENT, WITH WEAR TO THE UNDERLYING METAL PEGS RESULTING IN METALLOSIS. THE GLENOID COMPONENT WAS NOTED TO BE FRACTURED INTO TWO PARTS. REVISION SURGERY WAS PERFORMED WITH CONVERSION TO A REVERSE TOTAL SHOULDER ARTHROPLASTY. THE HUMERAL STEM FROM THE INDEX PROCEDURE WAS RETAINED IN SITU. THE PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT.
Patient problems: Metal Related Pathology; Pain
MAUDE report 25430030 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K042021. One submission often covers many models, so check the product and lot details in each record.
- Z-0537-2026 · Sep 5, 2025 · Open, ClassifiedBrand Name: Equinoxe Ergo Product Name: Ergo Augments Pilot Tip Converter Model/Catalog Number: 301-11-11 Software Version: N/A Product Description: Pilot Tip Converter Piece Compo
- Z-0536-2026 · Sep 5, 2025 · Open, ClassifiedBrand Name: Equinoxe Ergo Product Name: Adjustable Angle rTSA Reamer, 46mm Model/Catalog Number: 321-59-46 Software Version: N/A Product Description: rTSA Reamer, 46mm Component: N
- Z-0535-2026 · Sep 5, 2025 · Open, ClassifiedBrand Name: Equinoxe Ergo Product Name: Adjustable Angle rTSA Reamer, 42mm Model/Catalog Number: 321-59-42 Software Version: N/A Product Description: rTSA Reamer, 42mm Component: N
- Z-1403-2024 · Mar 6, 2024 · Open, ClassifiedExactech Equinoxe GLENOID,KEELED, CEMENTED, mates with 47, 50, 53 head, beta curvature, Sizes: a) Small, Item Number 314-01-12, b) Medium, Item Number 314-01-13, c) Large, Item Nu
- Z-1402-2024 · Mar 6, 2024 · Open, ClassifiedExactech Equinoxe GLENOID,KEELED, CEMENTED, Mates with 38, 41, 44 head, alpha curvature, Sizes: a), Small, Item Number 314-01-02; b) Medium, Item number 314-01-03; c) Large, Item
- Z-1404-2024 · Mar 6, 2024 · Open, ClassifiedExactech Equinoxe GLENOID,KEELED, CEMENTED, mates with 47, 50, 53 head, beta curvature, Sizes: a) Small, Item Number 314-02-02, b) Medium, Item Number 314-02-03, c) Large, Item Nu
- Z-1405-2024 · Mar 6, 2024 · Open, ClassifiedExactech Equinoxe GLENOID,KEELED, CEMENTED,47, 50, 53 head, beta curvature, Sizes: a) Small, Item Number 314-02-12, b) Medium, Item Number 314-02-13, c) Large, Item Number 314-02
- Z-0884-2021 · Nov 9, 2020 · Open, ClassifiedEquinoxe Humeral Stem, Primary, Press Fit, 11mm
- Z-1459-2015 · Feb 13, 2015 · TerminatedEquinoxe 44mm Short Humeral Head Catalog Number 310-01-44. Orthopedic shoulder implant component.
- Z-2115-2012 · Jun 15, 2012 · TerminatedEquinoxe Anatomic Replicator Plate Intended for Primary and Reverse Total Shoulder Arthroplasty
Other PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED devices
- DJO SURGICAL 508-32-204Encore Medical, L.P. · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 recall544 reports
- Comprehensive Reverse Shoulder 010000589Biomet Orthopedics, LLC · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 recall142 reports
- DELTA XTEND 130738203Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED175 reports
- DJO SURGICAL 509-00-432Encore Medical, L.P. · Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented1 recall117 reports
- Alliance® SBGL3007Zimmer, Inc. · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED162 reports
- DELTA XTEND 130760138Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED146 reports
- DELTA XTEND 130790030Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED132 reports
- DJO SURGICAL 509-00-436Encore Medical, L.P. · Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented124 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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