Equinoxe 321-35-38Recalls & reported problems
Exactech, Inc. · REAMER, REVERSE SHOULDER, MODULAR, CANNULATED, 38mm · Class 2
All models of Equinoxe (305)
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 10885862087805), received between Nov 10, 2022 and Sep 28, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (1 report).
18 other recalls cover devices cleared under the same FDA submission (K042021, K093430, K113309); 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.
Most reported problems
Device problems
- Break1
- Fracture1
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 28, 2023Break; Break
AS REPORTED DURING SURGICAL USE, THE SURGEON WAS REARING THE GLENOID AND WENT UP TO THE 38 REAMER AND IT CAUGHT A PIECE OF THE SUPERIOR GLENOID AND BOUND UP AT THE END OF HIS REAMING. SURGEON HANDED THE REAMER BACK TO THE TECH AND SHE NOTICED THAT THE REAMER HAD BROKEN WHEN IT CAUGHT THE SUPERIOR GLENOID. NO BROKEN PIECES, PARTS FELL INTO PATIENT WOUND SITE. THERE WAS NO SURGICAL DELAY/PROLONGATION. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. IMAGES RECEIVED. SALES REP WAS UNABLE TO OBTAIN X-RAYS. THE DEVICE WILL BE RETURN. NO OTHER PATIENT INFORMATION/MEDICAL HISTORY REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17840865 ↗MalfunctionNov 10, 2022Fracture; Fracture
IT WAS REPORTED THAT DURING A SURGICAL PROCEDURE, A SIZE 38 CANNULATED REAMER BROKE. FRAGMENTS, PARTS OR PIECES FELL INTO THE PATIENT WOUND SITE AND WERE REMOVED. THERE WAS A SURGICAL DELAY, AMOUNT OF TIME NOT REPORTED. ADVERSE EVENT AS A RESULT INDICATED ¿NO¿, ¿THERE ARE NO ADVERSE EVENTS AS A RESULT AS YET¿. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. THE DEVICE IS AVAILABLE FOR RETURN.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 15777263 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K042021, K093430, K113309. One submission often covers many models, so check the product and lot details in each record.
- 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-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-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-1415-2024 · Mar 6, 2024 · Open, ClassifiedExactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Right, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-32, b) 41, 44, 47, 50, head, Medium, Item Numbe
- Z-1413-2024 · Mar 6, 2024 · Open, ClassifiedExactech Equinoxe CAGE GLENOID, CEMENTED, beta curvature, Mates with: a) 47, 50, 53 head, Medium, Item Number 314-13-13, b) 47, 50, 53 head, Large, Item Number 314-13-14, c) 47
- 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-1414-2024 · Mar 6, 2024 · Open, ClassifiedExactech Equinoxe CAGE GLENOID,POSTERIOR AUGMENT, CEMENTED, Left, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-13-22, b) 41, 44, 47, 50, head, Medium, Item Number
- 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-1412-2024 · Mar 6, 2024 · Open, ClassifiedExactech Equinoxe CAGE GLENOID, CEMENTED, alpha curvature, Mates with: a) 38, 41, 44 head, Small, Item Number 314-13-02, b) 38, 41, 44 head, Medium, Item Number 314-13-03, c) 3
- Z-0884-2021 · Nov 9, 2020 · Open, ClassifiedEquinoxe Humeral Stem, Primary, Press Fit, 11mm
- Z-0459-2021 · Oct 6, 2020 · TerminatedCatalog 314-13-23, Equinoxe Cage Glenoid, Posterior Augment, Left, Medium
- Z-0460-2021 · Oct 6, 2020 · TerminatedCatalog 314-13-33, Equinoxe Cage Glenoid, Posterior Augment, Right, Medium
- Z-0414-2018 · Aug 31, 2017 · TerminatedEquinoxe Cage, Glenoid, Alpha, Small Product Usage: The Equinoxe Shoulder System is indicated for use in skeletally mature individuals with degenerative diseases or fractures of t
…and 3 more.
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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