Arthrex® AR-3200-1036Recalls & reported problems
Arthrex, Inc. · Synergy Matrix Management Software · Class 1
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 00888867253902), received between Nov 28, 2023 and Nov 28, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Unexpected Shutdown” (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
- Unexpected Shutdown1
Patient problems
- Insufficient Information1
- 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.
MalfunctionNov 28, 2023Unexpected Shutdown; Unexpected Shutdown
ON 11/1/2023, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA (B)(4) THAT AN AR-3200-1036 SYNERGY MATRIX MANAGEMENT SOFTWARE HAD AN ISSUE. DURING A CASE IN OR 3, 2 BOOM MONITORS WENT BLACK. INITIALLY ONLY ONE OF THE MONITORS WENT OUT AND THEN CAME BACK, THEN ANOTHER MONITOR WENT OUT, AND CAME BACK, THEN BOTH WENT OUT AT THE SAME TIME AND DIDN'T COME BACK. THE MONITORS WERE USING SDI AT THE TIME BECAUSE THE TECH NEVER ROUTED USING THE ELO. THE BLACKOUTS OCCURRED WHILE USING THE FAIL-OVER SDI MODE. THE CASE WAS COMPLETED WITH NO PATIENT HARM AS THE SALES REPRESENTATIVE ROUTED USING THE ELO.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 18220867 ↗
Other Medical device data system devices
- Trilogy100 Ventilator, Japan-RentalRespironics, Inc. · Medical device data system2 deaths334 reports
- Trilogy 100 Trilogy100 Ventilator, Bluetooth, ItalyRespironics, Inc. · Medical device data system146 reports
- AQURE 933-599Radiometer Medical ApS · Medical device data system2 recalls7 reports
- N/A A901Medtronic, Inc. · Medical device data system1 recall0 reports
- NA 9208000000Stryker Corporation · Medical device data system27 reports
- NA 9205000000Stryker Corporation · Medical device data system19 reports
- Trilogy 200 Trilogy 200 Ventilator, Italy, BluetoothRespironics, Inc. · Medical device data system13 reports
- NA 9206000000Stryker Corporation · Medical device data system9 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.
How reports and recalls are matched · Editorial policy · Report an error on this page