Equinoxe 321-09-40Recalls & reported problems
Exactech, Inc. · Humeral Liner Impactor Tip, 40mm · Class 2
All models of Equinoxe (305)
Data updated Oct 18, 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 10885862560223), received between Oct 2, 2020 and Oct 2, 2020 — 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 18, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- No Consequences Or Impact 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 2, 2020Break; Break
AS REPORTED, AT FINAL IMPACTION, THE IMPACTOR PIECE BROKE AND FELL TO THE FLOOR. NO PARTS OR PIECES FELL INTO THE WOUND. THE (B)(6) Y/O MALE PATIENT HAD A SUCCESSFUL SMALL BASEPLATE RSA WITH ALL IMPLANTS. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. DEVICE TO BE RETURNED. POST IMPLANT X-RAY WAS PROVIDED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10619194 ↗
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-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-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-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-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-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-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 320-42-00Exactech, Inc. · Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented3 recalls107 reports
- Equinoxe 320-38-00Exactech, 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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