Arthrex® AR-1665PSLRecalls & reported problems
Arthrex, Inc. · LNT Implant System, 4.75 PEEK SwiveLock · Class 2 · Implant
Data updated Oct 16, 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 00888867367319), received between Nov 22, 2023 and Nov 22, 2023 — 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Patient Device Interaction Problem1
Patient problems
- Unspecified Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 22, 2023Patient Device Interaction Problem; Patient Device Interaction Problem
ADDITIONAL INFORMATION RECEIVED ON 11/13/2023: THE INFECTIOUS DISEASE FACILITY REPRESENTATIVE DOES NOT KNOW WHERE THE PROCEDURE TOOK PLACE OR THE INFORMATION OF THE SURGEON. THE PROCEDURE WAS PERFORMED ON THE RIGHT SHOULDER, AND THE ARTHREX PRODUCTS ARE STILL IMPLANTED. THE INFECTION WAS IDENTIFIED ON (B)(6) 2023 BUT IT'S UNKNOWN IF IT'S DEEP OR SUPERFICIAL. THE INFECTION WAS TREATED WITH A RIGHT SHOULDER ARTHROSCOPIC AND OPEN I&D. ADDITIONAL INFORMATION WAS REQUESTED.
Patient problems: Unspecified Infection
MAUDE report 18190176 ↗
Other Fastener, fixation, biodegradable, soft tissue devices
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- HEALICOIL 72205137Smith & Nephew, Inc. · Fastener, fixation, biodegradable, soft tissue427 reports
- HEALIX ADVANCE ORTHOCORD 222296Medos International Sàrl · FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE320 reports
- TWINFIX 72202597Smith & Nephew, Inc. · FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE288 reports
- Arthrex® AR-2324BCCArthrex, Inc. · FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE254 reports
- HEALIX ADVANCE 222331Depuy Mitek, LLC · FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE1 recall196 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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