Arthrex® AR-7720-3.5Recalls & reported problems
Arthrex, Inc. · HUMERAL DRILL, 3.5 MM · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00888867042155), received between Oct 31, 2023 and Oct 31, 2023 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Dull, Blunt” (2 reports).
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
- Dull, Blunt2
- Smoking2
- Overheating of Device1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 31, 2023Smoking; Dull, Blunt; Smoking; Dull, Blunt
ON 10/2/2023, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA (B)(4).THAT AN AR-7720-3.5 HUMERAL DRILL AND AN AR-7720-4.0 HUMERAL DRILL, PART OF A RAR-7700S UCL RECONSTRUCTION SET (LOANER) HAD AN ISSUE. THE 3.5 AND 4.0 DRILLS WERE JUST DULL AND SMOKING DURING THE PROCEDURE. THAT HAPPENED DURING 3 CASES IN A ROW, AND IT WAS HAVING THE BONE SMOKE MORE THAN NORMAL. THE SET HAD BEEN INSPECTED UPON RECEIPT. THIS OCCURRED DURING USE IN AN UNSPECIFIED PROCEDURE WITH NO PATIENT HARM. ADDITIONAL INFORMATION HAS BEEN REQUESTED. ON 10/4/2023, THE SALES REPRESENTATIVE PROVIDED THE FOLLOWING INFORMATION VIA PHONE: THE SAME AR-7720-3.5 HUMERAL DRILL AND AN AR-7720-4.0 HUMERAL DRILL, PART OF A RAR-7700S UCL RECONSTRUCTION SET (LOANER, WITH LOT NUMBER 10225812) WERE USED IN THREE DIFFERENT COLLATERAL LIGAMENT REPAIR PROCEDURES ON (B)(6) 2023. THE INCREASED BONE SMOKE DID NOT BURN OR HARM THE PATIENTS, AND THERE WAS NO SMOKE OR BURNING SMELL NOTICED BY THE SURGEON OR THE FACILITY STAFF DURING THOSE CASES. THE THREE PATIENTS DID NOT OBTAIN ANY HARM. THE COMPLAINT DEVICES WERE USED TO COMPLETE EACH PROCEDURE SUCCESSFULLY. THERE WERE NO CASE DELAYS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18040923 ↗MalfunctionOct 31, 2023Smoking; Smoking
ON 10/2/2023, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA (B)(4) THAT AN AR-7720-3.5 HUMERAL DRILL AND AN AR-7720-4.0 HUMERAL DRILL, PART OF A RAR-7700S UCL RECONSTRUCTION SET (LOANER) HAD AN ISSUE. THE 3.5 AND 4.0 DRILLS WERE JUST DULL AND SMOKING DURING THE PROCEDURE. THAT HAPPENED DURING 3 CASES IN A ROW, AND IT WAS HAVING THE BONE SMOKE MORE THAN NORMAL. THE SET HAD BEEN INSPECTED UPON RECEIPT. THIS OCCURRED DURING USE IN AN UNSPECIFIED PROCEDURE WITH NO PATIENT HARM. ADDITIONAL INFORMATION HAS BEEN REQUESTED. ON 10/4/2023, THE SALES REPRESENTATIVE PROVIDED THE FOLLOWING INFORMATION VIA PHONE: THE SAME AR-7720-3.5 HUMERAL DRILL AND AN AR-7720-4.0 HUMERAL DRILL, PART OF A RAR-7700S UCL RECONSTRUCTION SET (LOANER, WITH LOT NUMBER 10225812) WERE USED IN THREE DIFFERENT COLLATERAL LIGAMENT REPAIR PROCEDURES ON (B)(6)2023. THE INCREASED BONE SMOKE DID NOT BURN OR HARM THE PATIENTS, AND THERE WAS NO SMOKE OR BURNING SMELL NOTICED BY THE SURGEON OR THE FACILITY STAFF DURING THOSE CASES. THE THREE PATIENTS DID NOT OBTAIN ANY HARM. THE COMPLAINT DEVICES WERE USED TO COMPLETE EACH PROCEDURE SUCCESSFULLY. THERE WERE NO CASE DELAYS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18040546 ↗MalfunctionOct 31, 2023Overheating of Device; Dull, Blunt; Overheating of Device; Dull, Blunt
ON 10/2/2023, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA (B)(4) THAT AN AR-7720-3.5 HUMERAL DRILL AND AN AR-7720-4.0 HUMERAL DRILL, PART OF A RAR-7700S UCL RECONSTRUCTION SET (LOANER) HAD AN ISSUE. THE 3.5 AND 4.0 DRILLS WERE JUST DULL AND SMOKING DURING THE PROCEDURE. THAT HAPPENED DURING 3 CASES IN A ROW, AND IT WAS HAVING THE BONE SMOKE MORE THAN NORMAL. THE SET HAD BEEN INSPECTED UPON RECEIPT. THIS OCCURRED DURING USE IN AN UNSPECIFIED PROCEDURE WITH NO PATIENT HARM. ADDITIONAL INFORMATION HAS BEEN REQUESTED. ON 10/4/2023, THE SALES REPRESENTATIVE PROVIDED THE FOLLOWING INFORMATION VIA PHONE: THE SAME AR-7720-3.5 HUMERAL DRILL AND AN AR-7720-4.0 HUMERAL DRILL, PART OF A RAR-7700S UCL RECONSTRUCTION SET (LOANER, WITH LOT NUMBER 10225812) WERE USED IN THREE DIFFERENT COLLATERAL LIGAMENT REPAIR PROCEDURES ON (B)(6) 2023. THE INCREASED BONE SMOKE DID NOT BURN OR HARM THE PATIENTS, AND THERE WAS NO SMOKE OR BURNING SMELL NOTICED BY THE SURGEON OR THE FACILITY STAFF DURING THOSE CASES. THE THREE PATIENTS DID NOT OBTAIN ANY HARM. THE COMPLAINT DEVICES WERE USED TO COMPLETE EACH PROCEDURE SUCCESSFULLY. THERE WERE NO CASE DELAYS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18040522 ↗
Other BIT, DRILL devices
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- QUICKSET 2274-35-500Depuy Orthopaedics, Inc. · BIT, DRILL770 reports
- QUICKSET 2274-30-500Depuy Orthopaedics, Inc. · BIT, DRILL761 reports
- NA 03.037.022Synthes GmbH · BIT, DRILL339 reports
- NA 323.062Synthes GmbH · BIT, DRILL309 reports
- QUICKSET 2274-56-000Depuy (Ireland) · BIT, DRILL275 reports
- QUICKSET 2274-45-500Depuy Orthopaedics, Inc. · BIT, DRILL211 reports
- LCS 2366-83-000Depuy (Ireland) · BIT, DRILL207 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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