Arthrex® AR-8719DS-181815Recalls & reported problems
Arthrex, Inc. · Dynanite NiTi Staple w/Instrs 18Wx18/15L · Class 2 · Implant
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 00888867288188), received between May 23, 2022 and May 23, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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.
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
- Break1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 23, 2022Break; Appropriate Device Problem Term/Code Not Available
ON (B)(6) 2022, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA PHONE THAT AN AR-8771-0422X DYNAMITE COMPRESSION PLATE WAS IMPLANTED ON PATIENT DURING A TARSAL METATARSAL FUSION PROCEDURE ON (B)(6) 2021. ON (B)(6) 2022, IT WAS NOTICED TO BE BROKEN VIA X-RAY. PATIENT UNDERWENT TARSAL METATARSAL FUSION REVISION SURGERY ON (B)(6) 2022 AND HAD THE AR-8771-0422X DYNAMITE COMPRESSION PLATE ALONG WITH THE STAPLES FROM AN AR-8719DS-181815 DYNAMITE NITINOL STAPLE IMPLANT SYSTEM REMOVED. SURGEON COMPLETED THE REVISION SURGERY BY IMPLANTING DEVICES FROM ANOTHER MANUFACTURER. CASE WAS COMPLETED SUCCESSFULLY AND NO FURTHER ISSUES HAS BEEN REPORTED.
Patient problems: Insufficient Information
MAUDE report 14469444 ↗
Other Staple, fixation, bone devices
- N/A StandardSynthes GmbH · Staple, Fixation, Bone2 recalls16 reports
- 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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