Equinoxe 321-55-38Recalls & reported problems
Exactech, Inc. · REAMER, MODULAR, REVERSE, CANNULATED, NARROW, 38mm · Class 2
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
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885862232762), received between Oct 30, 2019 and Oct 30, 2019 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (1 report).
13 other recalls cover devices cleared under the same FDA submission (K063569); 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
Patient problems
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 30, 2019Break
IT WAS REPORTED THAT THE SURGEON PUT A BOW TIE REAMER ON A MODULAR HANDLE (ON DRILL NOT REAM). PUT IT OVER A K WIRE AND RAN IT DOWN TO THE GLENOID. STARTED TO REAM THE GLENOID AND THE PIECE THAT ATTACHES TO THE HANDLE SHEARED OFF. IT DID END UP NOTCHING THE GLENOID BUT WE WERE ABLE TO FACILITATE THE BASEPLATE ON WITHOUT COMPLICATIONS.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 9257092 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K063569. One submission often covers many models, so check the product and lot details in each record.
- Z-2561-2025 · Aug 15, 2025 · Open, ClassifiedExactech Equinoxe, Reverse Shoulder Humeral Liners, REF: 320-38-00,145-DEG PE 38MM HUM LINER +0/ 320-38-03,145-DEG PE 38MM HUM LINER +2.5/ 320-42-00,145-DEG PE 42MM HUM LINER +0/
- Z-1423-2024 · Mar 6, 2024 · Open, ClassifiedExactech Equinoxe REVERSE SHOULDER,42mm Constrained Humeral Liner, a) +0mm, Item number 320-42-10, b) +2.5mm, Item Number 320-42-13; Shoulder Arthroplasty
- Z-1424-2024 · Mar 6, 2024 · Open, ClassifiedExactech Equinoxe REVERSE SHOULDER,46mm Humeral Liner, a) +0mm, Item number 320-46-00, b) +2.5mm, Item Number 320-46-03; Shoulder Arthroplasty
- Z-1418-2024 · Mar 6, 2024 · Open, ClassifiedExactech Equinoxe REVERSE SHOULDER, 38mm Humeral Liner: a) +0mm, Item Number 320-38-00, b) +2.5mm, Item Number 320-38-03; Shoulder Arthroplasty
- Z-1422-2024 · Mar 6, 2024 · Open, ClassifiedExactech Equinoxe REVERSE SHOULDER,42mm Humeral Liner, a) +0mm, Item number 320-42-00, b) +2.5mm, Item Number 320-42-03; Shoulder Arthroplasty
- Z-1425-2024 · Mar 6, 2024 · Open, ClassifiedExactech Equinoxe REVERSE SHOULDER,46mmConstrained Humeral Liner, a) +0mm, Item number 320-46-10, b) +2.5mm, Item Number 320-46-13; Shoulder Arthroplasty
- Z-1419-2024 · Mar 6, 2024 · Open, ClassifiedExactech Equinoxe REVERSE SHOULDER,38mm Constrained Humeral Liner: a) +0mm, Item Number 320-38-10, b) +2.5mm, Item Number 320-38-13, Shoulder Arthroplasty
- Z-0579-2024 · Nov 21, 2023 · Open, ClassifiedExactech Equinoxe Reverse Shoulder System, Catalog Numbers: a) 320-36-00, b) 320-36-03, c) 320-36-04, d) 320-36-10, e) 320-36-13, f) 320-38-00, g) 320-38-13, h) 320-40-00,
- Z-3019-2020 · Aug 24, 2020 · TerminatedEquinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 18 mm.
- Z-3020-2020 · Aug 24, 2020 · TerminatedEquinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 22 mm.
- Z-0012-2019 · Aug 21, 2018 · Open, ClassifiedEquinoxe Reverse Drill Bit Kit, Catalog Number 321-20-00 Product Usage: Shoulder surgery
- Z-0900-2017 · Oct 25, 2016 · TerminatedEquinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit
- Z-2117-2012 · Jun 15, 2012 · TerminatedEquinoxe Reverse Compression Screw Intended for Primary and Reverse Total Shoulder Arthroplasty.
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 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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