Equinoxe 320-46-00Recalls & reported problems

Summary

The FDA's MAUDE database contains 22 adverse event reports that list this exact device (DI 10885862086730), received between Aug 19, 2020 and Aug 3, 2026 — classified as 22 injuries.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (13 reports).

1 FDA recall record name this device's identifier, 1 still open.

12 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.

Recalls naming this device

1. Mar 6, 2024Open, Classified

   The packaging of these affected UHMWPE humeral liners and glenoids are nonconforming as they do not meet the established packaging specification. They were packaged in vacuum bags that did not contain an additional oxygen barrier layer consisting of Ethylene Vinyl Alcohol (EVOH).

   Z-1424-2024 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗

Most reported problems

Recent adverse event reports

The 22 most recent of 22 reports, in the reporter's own words as published by the FDA.

• InjuryAug 3, 2026Detachment of Device or Device Component

  As reported by the Equinoxe Shoulder Study, the patient underwent an initial right reverse total shoulder arthroplasty. Subsequently, the patient was revised due to poly dissociation. The humeral liner and humeral tray were removed. The outcome is considered to be continuing.

  Patient problems: Insufficient Information

  MAUDE report 50113333 ↗
• InjurySep 3, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED A PATIENT UNDERWENT A LEFT TOTAL SHOULDER ARTHROPLASTY. SUBSEQUENTLY, ONE (1) YEAR, SIX (6) MONTHS LATER, THE PATIENT EXPERIENCED PAIN. AS A RESULT, THE PATIENT UNDERWENT REVISION OF THE LEFT KNEE. THE PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION. NO MEDICAL OR SURGICAL INTERVENTIONS WERE REPORTED. EXPLANTS WERE PROVIDED FOR EVALUATION. NO ADDITIONAL INFORMATION IS AVAILABLE.

  Patient problems: Pain

  MAUDE report 22952344 ↗
• InjuryJul 1, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT THE PATIENT RECEIVED AN INITIAL RIGHT RTSA APPROXIMATELY 3 YEARS AND 9 MONTHS AGO. SUBSEQUENTLY, IT WAS REPORTED THAT THE POLYETHYLENE LINER DISASSOCIATED FROM THE HUMERAL TRAY APPROXIMATELY 3 YEARS AND 7 MONTHS AFTER INITIAL IMPLANTATION. AS A RESULT, THE PATIENT UNDERWENT A RIGHT SHOULDER REVISION TO REPLACE THE POLYETHYLENE LINER APPROXIMATELY 3 YEARS AND 8 MONTHS AFTER INITIAL IMPLANTATION. NO FURTHER PATIENT IMPACT REPORTED. NO FURTHER INFORMATION AVAILABLE.

  Patient problems: Insufficient Information

  MAUDE report 22376621 ↗
• InjuryApr 30, 2025Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT THE PATIENT UNDERWENT AN INITIAL TOTAL SHOULDER REPLACEMENT ON THE RIGHT SIDE. SUBSEQUENTLY, THE PATIENT EXPERIENCED DISASSOCIATION OF POLYETHYLENE - RSP. AS A RESULT, APPROXIMATELY 2 YEARS AFTER INITIAL REPLACEMENT, THE PATIENT UNDERWENT A SHOULDER REVISION. NO FURTHER IMPACT TO THE PATIENT WAS REPORTED. NO OTHER INFORMATION IS AVAILABLE.

  Patient problems: Insufficient Information

  MAUDE report 21938720 ↗
• InjuryApr 30, 2025Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THIS PATIENT'S RIGHT SHOULDER WAS REVISED APPROXIMATELY 3 YEARS 4 MONTHS POST OPERATION. SUBSEQUENTLY, THE HUMERAL TRAY DETACHED FROM THE HUMERAL STEM. THE PATIENT'S PROSTHESIS WAS NOT ARTICULATING AS INTENDED. SURGEON REMOVED, THE TRAY, LINER, TORQUE SCREW, GLENOSPHERE LOCKING SCREW, AND GLENOSPHERE. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT.

  Patient problems: Joint Dislocation; Joint Laxity

  MAUDE report 21938510 ↗
• InjuryNov 1, 2024Detachment of Device or Device Component; Adverse Event Without Identified Device or Use Problem; Detachment of Device or Device Component; Adverse Event Without Identified Device or Use Problem

  APPROXIMATELY 1 YEAR(S), 10 MONTH(S) AND 1 DAY(S) POST-OPERATIVE OF A REVISED LEFT TSA, IT WAS REPORTED VIA CLINICAL STUDY THAT THE PATIENT EXPERIENCED UNEXPLAINED PAIN. PATIENT PRESENTED WITH PAIN AFTER WORKING LONG SHIFT, PREVIOUS FALL FROM TREE - DATE UNKNOWN. PREVIOUS REVISION INFORMATION WAS NOT AVAILABLE AT THIS TIME. THE PATIENT UNDERWENT ANOTHER STANDARD REVERSE REVISION, AND THE OUTCOME OF THIS EVENT IS CONSIDERED RESOLVED. THE CLINICAL REPORT INDICATES THAT THIS EVENT IS DEFINITELY NOT RELATED TO THE DEVICE(S) AND/OR TO THE PROCEDURE. AS THERE IS NO WRITTEN, ELECTRONIC, OR ORAL COMMUNICATION THAT ALLEGES DEFICIENCIES RELATED TO THE IDENTITY, QUALITY, DURABILITY, RELIABILITY, SAFETY, EFFECTIVENESS, OR PERFORMANCE OF A DEVICE AFTER IT IS RELEASED FOR DISTRIBUTION, THIS DEVICE ISSUE IS NOT CONSIDERED A COMPLAINT.

  Patient problems: Pain

  MAUDE report 20587215 ↗
• InjuryOct 15, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  APPROXIMATELY 3 YEAR(S), 10 MONTH(S) AND 5 DAY(S) POST-OPERATIVE OF A LEFT RTSA, IT WAS REPORTED VIA CLINICAL STUDY THAT THE PATIENT EXPERIENCED DISASSOCIATION OF POLYETHYLENE. PATIENT TRIED TO BRACE HIMSELF FROM FALLING OFF A LADDER. THE PATIENT UNDERWENT A STANDARD REVERSE WITH PRESERVE STEM REVISION WITH THE REPORTED REMOVAL OF THE HUMERAL TRAY, HUMERAL LINER, GLENOSPHERE, AND GLENOSPHERE LOCKING SCREW. THE OUTCOME OF THIS EVENT IS CONSIDERED RESOLVED AND THE CLINICAL REPORT INDICATES THAT THIS EVENT IS POSSIBLY RELATED TO THE DEVICE(S) AND POSSIBLY RELATED TO THE PROCEDURE.

  Patient problems: Insufficient Information

  MAUDE report 20456508 ↗
• InjurySep 23, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  APPROXIMATELY 3 YEAR(S), 8 MONTH(S) AND 13 DAY(S) POST-OPERATIVE OF A LEFT RTSA, IT WAS REPORTED VIA CLINICAL STUDY THAT THE PATIENT EXPERIENCED DISASSOCIATION OF POLYETHYLENE. SUBJECT WAS GOLFING, HEARD POPPING AND PAIN. THE PATIENT UNDERWENT A STANDARD REVERSE WITH PRESERVE STEM REVISION WITH THE REMOVAL OF THE PRESERVE STEM (RTSA), HUMERAL TRAY, HUMERAL LINER, GLENOSPHERE, GLENOSPHERE LOCKING SCREW, AND GLENOID BASE PLATE. THE OUTCOME OF THIS EVENT IS CONSIDERED RESOLVED AND THE CLINICAL REPORT INDICATES THAT THIS EVENT IS DEFINITELY RELATED TO THE DEVICE(S) AND DEFINITELY NOT RELATED TO THE PROCEDURE.

  Patient problems: Implant Pain

  MAUDE report 20280052 ↗
• InjuryAug 14, 2024Detachment of Device or Device Component; Detachment of Device or Device Component

  IT WAS REPORTED THAT THIS PATIENT'S SHOULDER WAS REVISED. THE HUMERAL INLAY IS DISLOCATED FROM HUMERAL PLATE. HUMERAL PLATE/HUMERAL INLAY AND GLENOSPHERE HAD TO BE REPLACED.

  Patient problems: Insufficient Information

  MAUDE report 19986706 ↗
• InjuryMay 3, 2024Detachment of Device or Device Component; Device Dislodged or Dislocated; Detachment of Device or Device Component; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THIS 73 Y/O PATIENT'S RIGHT SHOULDER WAS REVISED APPROXIMATELY 9 MONTHS POST OP. AFTER XRAY IT WAS DETERMINED THE POLY DISASSOCIATED FROM THE TRAY. THEY ARE NOT SURE WHEN THE EVENT OCCURRED BUT THE PATIENT CAME TO THE DOCTORS OFFICE WITH PAIN AND CLICKING. THE TRAY WAS REMOVED AND THE GLENOSPHERE TAKEN OFF TO EVALUATE THE STEM AND GLENOID PLATE. BOTH WERE FOUND TO BE WELL FIXED. THEN THE SURGEON TRIALED A 42+4 AND FOUND IT TO HAVE EXCELLENT ROM. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Failure of Implant; Pain

  MAUDE report 19243920 ↗
• InjuryApr 16, 2024Naturally Worn; Adverse Event Without Identified Device or Use Problem; Naturally Worn; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT AN 80 YO MALE PATIENT, INITIAL SHOULDER IMPLANTED ON (B)(6) 2017, UNDERWENT A REVISION PROCEDURE ON (B)(6) 2024, APPROXIMATELY 6 YEARS 10 MONTHS POST THE INITIAL PROCEDURE. THE PATIENT WAS REVISED DUE TO ISSUES SINCE THEIR PRIMARY SURGERY, COULD BE INFECTION, BUT THE SURGEON WANTS TO MAKE A REPORT JUST IN CASE. THE SURGEON SUSPECTS POSSIBLE POLY WEAR. THERE WERE NO DEVICE BREAKAGES OR SURGICAL DELAYS DURING THE PROCEDURE. NO X-RAYS WERE PROVIDED. THE PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. NO EXPLANTED DEVICES ARE AVAILABLE FOR ANALYSIS AS THEY WERE SENT TO PATHOLOGY AT THE HOSPITAL. DEVICE IMAGES WERE PROVIDED. NO FURTHER INFORMATION.

  Patient problems: Unspecified Infection

  MAUDE report 19121871 ↗
• InjuryMar 14, 2024Detachment of Device or Device Component; Device Dislodged or Dislocated; Naturally Worn; Detachment of Device or Device Component; Device Dislodged or Dislocated; Naturally Worn

  AS REPORTED BY THE EQUINOXE SHOULDER STUDY, THE 58-YEAR-OLD MALE PATIENT HAD A RIGHT TSA ON (B)(6) 2022. THE PATIENT PRESENTED WITH DISASSOCIATION OF POLYETHYLENE - PATIENT HAS EXPERIENCED CHRONIC INSTABILITY OF THE SHOULDER SINCE POD2, THEN IN ONE SUBLUXATION EVENT, THE POLYETHYLENE DISSOCIATED. THE OUTCOME OF THIS EVENT IS CONSIDERED RESOLVED AND THE REPORT INDICATES THAT THE ACTION TAKEN IS REVISION ON (B)(6) 2024. THE CASE REPORT FORM INDICATES THAT THIS EVENT IS DEFINITELY RELATED TO THE DEVICE AND/OR TO THE PROCEDURE. THIS EVENT REPORT WAS RECEIVED THROUGH CLINICAL DATA COLLECTION ACTIVITIES AND NO DEVICE RETURN IS ANTICIPATED.

  Patient problems: Failure of Implant; Joint Dislocation; Joint Laxity

  MAUDE report 18909371 ↗
• InjuryMar 7, 2024Detachment of Device or Device Component; Device Dislodged or Dislocated; Detachment of Device or Device Component; Device Dislodged or Dislocated

  AS REPORTED BY THE EQUINOXE SHOULDER STUDY, THE PATIENT HAD A LEFT TSA ON (B)(6) 2018 AND PRESENTED WITH DISASSOCIATION OF POLYETHYLENE, ON (B)(6) 2019, PATIENT REACHED BACK AND HAD A SHARP PAIN. THE OUTCOME OF THIS EVENT IS CONSIDERED RESOLVED ON (B)(6) 2021. THE ACTION TAKEN WAS REVISION-STANDARD REVERSE WITH THE REMOVAL OF THE TORQUE SCREW, HUMERAL TRAY, HUMERAL LINER, GLENOSPHERE, GLENOSPHERE LOCKING SCREW. THE CASE REPORT FORM INDICATES THAT THIS EVENT IS POSSIBLY RELATED TO THE DEVICE AND DEFINITELY NOT RELATED TO THE PROCEDURE. THIS EVENT REPORT WAS RECEIVED THROUGH CLINICAL DATA COLLECTION ACTIVITIES AND NO DEVICE RETURN IS ANTICIPATED.

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Failure of Implant; Pain

  MAUDE report 18862796 ↗
• InjuryDec 19, 2023Unstable; Device Dislodged or Dislocated; Unstable; Device Dislodged or Dislocated

  AS REPORTED BY THE EQUINOXE SHOULDER STUDY, THE PATIENT, (B)(6), HAD AN INITIAL LEFT TSA ON (B)(6) 2017. PATIENT (B)(6) PRESENTED ON (B)(6) 2017 WITH INSTABILITY DESCRIBED AS HAVING SUBLUXATION THAT ARE SELF-REDUCED. THE CASE REPORT FORM INDICATES THAT THIS EVENT IS POSSIBLY RELATED TO DEVICE AND DEFINITELY RELATED TO PROCEDURE. OUTCOME IS CONTINUING; PATIENT ADVISED TO SCHEDULE REVISION (POLY EXCHANGE). DUE TO CLINICAL STUDY, NO DEVICES WILL BE RETURNED FOR EVALUATION.

  Patient problems: Joint Dislocation; Joint Laxity; Subluxation

  MAUDE report 18358647 ↗
• InjuryNov 28, 2022Detachment of Device or Device Component; Detachment of Device or Device Component

  AS REPORTED BY THE EQUINOXE SHOULDER STUDY, APPROXIMATELY FIVE YEARS POST INITIAL RIGHT SIDE TSA, THE 62 Y/O MALE PATIENT WAS LIFTING A SIGN OVERHEAD AND HAD SHARP PAIN. PATIENT EXPERIENCED DISASSOCIATION OF POLYETHYLENE. PATIENT HAD A REVISION APPROXIMATELY A MONTH LATER AND THE EVENT WAS RESOLVED.

  Patient problems: Failure of Implant; Pain

  MAUDE report 15874689 ↗
• InjuryJun 7, 2022Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THAT THIS PATIENT HAD A REVISION WHICH WAS NOT PREVIOUSLY REPORTED. REASON HAS NOT BEEN REPORTED. THIS WAS FOUND DURING THE INVESTIGATION OF (B)(4). (MDR# 1038671-2022-00072).

  Patient problems: Failure of Implant

  MAUDE report 14620282 ↗
• InjuryApr 21, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

  AS REPORTED, APPROXIMATELY ONE YEAR POST OP THE INITIAL TSA, THIS MALE PATIENT'S WAS REVISED DUE TO HUMERAL LINER DISASSOCIATION. PATIENT WAS PERFORMING OVERHEAD ACTIVITY 2 WEEKS AGO AND FELT SOMETHING IN HIS SHOULDER. PRESENTED TO CLINIC WITH PAIN AND X-RAY SHOWING POSSIBLE LINER DISASSOCIATION. HE WAS REVISED YESTERDAY BY SURGEON TO A NEW O TRAY AND 46 MM LINER OF SAME SIZE. NO FURTHER INFORMATION AVAILABLE. EXPLANT IS NOT GIVEN TO REP WITHOUT PATIENT PERMISSION. PATIENT LAST KNOWN TO BE IN STABLE CONDITION.

  Patient problems: Failure of Implant

  MAUDE report 14166459 ↗
• InjuryMar 15, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED THAT THIS (B)(6) MALE PATIENT'S RIGHT SHOULDER WAS REVISED DUE TO HIS HUMERAL LINER BECOMING DISASSOCIATED FROM THE HUMERAL TRAY SOMETIME AFTER PRIMARY SURGERY. SURGEON REMOVED THE STEM, TRAY, AND LINER. DATE OF REVISION IS UNKNOWN AND INITIAL IMPLANT DATE IS UNKNOWN. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. DEVICES WILL BE RETURNING.

  Patient problems: Failure of Implant

  MAUDE report 13769965 ↗
• InjuryDec 6, 2021Device Dislodged or Dislocated; Device Dislodged or Dislocated

  AS REPORTED, AFTER AN UNKNOWN AMOUNT OF TIME FROM THE PRIMARY LEFT TSA SURGERY, THIS (B)(6) Y/O MALE PATIENT'S LEFT HUMERAL LINER SEPARATED FROM THE HUMERAL TRAY. THE SURGEON REMOVED THE PRESERVE STEM, ZERO HUMERAL TRAY, 46 NEUTRAL HUMERAL LINER AND 46 INSET GLENOSPHERE AND WAS REPLACED WITH A 42+4 GLENOSPHERE. THERE WAS ¿NO BREAKAGE OR SURGICAL DELAY¿. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT.

  Patient problems: Failure of Implant

  MAUDE report 12933345 ↗
• InjurySep 7, 2021Device Dislodged or Dislocated; Device Dislodged or Dislocated

  AS REPORTED, THIS (B)(6) Y/O MALE PATIENT WAS REACHING FOR SOMETHING WITH HIS L ARM IN FORWARD ELEVATION AND EXTERNAL ROTATION AND SUSTAINED AN INSTABILITY EVENT. DISASSOCIATION OF POLYETHYLENE WAS DIAGNOSED AND THE PATIENT WAS REVISED. THE CASE REPORT FORM INDICATES THIS EVENT IS DEFINITELY RELATED TO DEVICES OR PROCEDURE. THIS EVENT REPORT WAS RECEIVED THROUGH CLINICAL DATA COLLECTION ACTIVITIES.

  Patient problems: Failure of Implant

  MAUDE report 12431973 ↗
• InjuryApr 16, 2021Device Dislodged or Dislocated; Device Dislodged or Dislocated

  AS REPORTED, THIS (B)(6) Y/O MALE PATIENT¿S RIGHT SHOULDER WAS REVISED DUE TO THE LINER SEPARATING FROM THE HUMERAL TRAY SOMETIME AFTER THE INITIAL SURGERY. THE SURGEON REMOVED A 46 GLENOSPHERE, 46 NEUTRAL LINER AND A +0 ADAPTER TRAY. HE REPLACED THEM WITH A 42+4 GLENOSPHERE, 42+2.5 HUMERAL LINER AND A +10MM ADAPTER TRAY. THE PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT.

  Patient problems: Failure of Implant

  MAUDE report 11677303 ↗
• InjuryAug 19, 2020Detachment of Device or Device Component; Detachment of Device or Device Component

  AS REPORTED, APPROXIMATELY 9 MONTHS POSTOP A RIGHT TSA, THIS (B)(6) Y/O MALE PATIENT WAS INFECTED WITH COVID 19 AND ADMITTED TO ICU. THE PATIENT WAS ON VENTILATOR FOR 2 WEEKS. WHEN HE WAS DISCHARGED FROM THE HOSPITAL, HE DESCRIBED HIS RIGHT SHOULDER AS ¿NOT FEELING RIGHT¿. UPON X-RAY EXAMINE, THE DISASSOCIATED IMPLANTS WERE EVIDENT. THE PATIENT WAS FINE PRIOR TO HAVING COVID. THE TORQUE SCREW BACKED OUT AND THE TRAY AND LINER DISASSOCIATED FROM THE STEM. A REVISION WAS COMPLETED WITH REPLACEMENT OF THE TORQUE SCREW, TRAY AND LINER. ALL PARTS OR PIECES WERE REMOVED FROM THE WOUND SITE. THE PATIENT UNDERWENT SUCCESSFUL REVISION AND REPLACEMENT OF FAILED IMPLANTS AND IS DOING WELL. DEVICES TO BE RETURNED.

  Patient problems: Device Embedded In Tissue or Plaque

  MAUDE report 10425487 ↗

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, Classified
  Exactech 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, Classified
  Exactech 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, Classified
  Exactech Equinoxe REVERSE SHOULDER,42mm Humeral Liner, a) +0mm, Item number 320-42-00, b) +2.5mm, Item Number 320-42-03; Shoulder Arthroplasty
• Z-1419-2024 · Mar 6, 2024 · Open, Classified
  Exactech 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, Classified
  Exactech Equinoxe REVERSE SHOULDER, 38mm Humeral Liner: a) +0mm, Item Number 320-38-00, b) +2.5mm, Item Number 320-38-03; Shoulder Arthroplasty
• Z-1423-2024 · Mar 6, 2024 · Open, Classified
  Exactech 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-0579-2024 · Nov 21, 2023 · Open, Classified
  Exactech 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 · Terminated
  Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 18 mm.
• Z-3020-2020 · Aug 24, 2020 · Terminated
  Equinoxe Reverse Shoulder Compression Screw/Locking Cap Kit 4.5 x 22 mm.
• Z-0012-2019 · Aug 21, 2018 · Open, Classified
  Equinoxe Reverse Drill Bit Kit, Catalog Number 321-20-00 Product Usage: Shoulder surgery
• Z-0900-2017 · Oct 25, 2016 · Terminated
  Equinoxe Reverse Shoulder Fixed Angle Torque Defining Screw Kit
• Z-2117-2012 · Jun 15, 2012 · Terminated
  Equinoxe Reverse Compression Screw Intended for Primary and Reverse Total Shoulder Arthroplasty.