Equinoxe 321-52-07Recalls & reported problems
Exactech, Inc. · 3.2mm K Wire Drill · Class 2
- 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 10885862563811), received between Sep 18, 2026 and Sep 18, 2026 — classified as 1 injury.
The most frequently reported specific device problem is “Fracture” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Fracture1
Patient problems
- Foreign Body In Patient1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 18, 2026Fracture
It was reported that a drill bit fractured during use. Specifically, the tip of the drill bit broke off and remained embedded in the patients glenoid. The fragment was not retrieved, as it was determined that attempting removal could have caused greater harm to the patient. The patient was reported to be functioning well following surgery. The patient was last known to be in stable condition following the event. No further information is available.
Patient problems: Foreign Body In Patient; No Clinical Signs, Symptoms or Conditions
MAUDE report 50820974 ↗
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-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-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-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-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-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-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-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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.