Arthrex® AR-1665BCPLRecalls & reported problems
Arthrex, Inc. · LNT Implant System, 2.9 BC PushLock · Class 2 · Implant
Data updated Oct 16, 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 00888867367258), received between Oct 15, 2025 and Oct 15, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Failure to Advance” (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
- Failure to Advance1
Patient problems
- 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.
MalfunctionOct 15, 2025Failure to Advance; Failure to Advance
ON 09/29/2025, A SALES REPRESENTATIVE REPORTED VIA PHONE THAT AN AR-1665BCPL 2.9 BC LOOP 'N' TACK¿ TENODESIS IMPLANT SYSTEMS SWIFT STITCH DID NOT ADVANCE. THIS OCCURRED BEFORE USE OUT OF THE BOX DURING A BICEPS TENODESIS PROCEDURE ON (B)(6) 2025. THE PROCEDURE CONTINUED WITH A TENOTOMY PERFORMED. THERE WAS NO DELAY IN THE CASE. THERE WAS NO HARM ON THE PATIENT. ADDITIONAL INFORMATION HAS BEEN REQUESTED. ADDITIONAL INFORMATION WAS PROVIDED ON 09/29/2025 WHERE IT WAS REPORTED THAT DUE TO THE DEFECTIVE KIT FIRST AND BICEP PATHOLOGY, A TENOTOMY WAS DECIDED TO BE PREFORMED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23292452 ↗
Other Fastener, fixation, biodegradable, soft tissue devices
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- HEALIX ADVANCE ORTHOCORD 222295Medos International Sàrl · FASTENER, FIXATION, BIODEGRADABLE, SOFT TISSUE640 reports
- 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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