Arthrex® AR-8719MXDS-1815Recalls & reported problems
Arthrex, Inc. · SuperMX NiTi Staple w/ Instrs, 18W x 15L · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 00888867300873), received between Dec 4, 2024 and Dec 4, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (1 report).
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.
Reports received per month
Most reported problems
Device problems
- Patient Device Interaction Problem1
Patient problems
- Hypersensitivity/Allergic reaction1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryDec 4, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
ON (B)(6) 2024, A PATIENT SUBMITTED AN INQUIRY VIA EMAIL REQUESTING THE MATERIAL COMPOSITION OF A 4.5 CANNULATED SCREW THAT WAS USED THE PROCEDURE. NO ALLEGATION OF PRODUCT DEFICIENCY OR ADVERSE EVENT WAS REPORTED WITHIN THIS INQUIRY. ADDITIONAL INFORMATION RECEIVED ON 11/6/2024: THE PATIENT WAS IMPLANTED WITH TWO TITANIUM SCREWS AND AN AR-8719MXDS-1815 DYNANITE SUPERMX NITINOL STAPLE. THE PATIENT DEVELOPED COMPLICATIONS DUE TO AN ALLERGIC REACTION. THE PATIENT UNDERWENT REVISION SURGERY. NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: Hypersensitivity/Allergic reaction
MAUDE report 20844634 ↗
Other Staple, fixation, bone devices
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- GII QUICKANCHOR ETHIBOND 212034Medos International Sàrl · STAPLE, FIXATION, BONE98 reports
- GII QUICKANCHOR ORTHOCORD 222983Medos International Sàrl · STAPLE, FIXATION, BONE94 reports
- Speed SE-0910Synthes GmbH · Staple, Fixation, Bone1 recall24 reports
- Speed Shift SE-2020-10Synthes GmbH · Staple, Fixation, Bone1 recall10 reports
- Lapiplasty SpeedPlate SK50Treace Medical Concepts, Inc. · Staple, Fixation, Bone59 reports
- Speed SE-1512Synthes GmbH · Staple, Fixation, Bone1 recall6 reports
- LUPINE ORTHOCORD 210709Depuy Mitek, LLC · STAPLE, FIXATION, BONE56 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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