Sherlock 9770130Recalls & reported problems
Bard Access Systems, Inc. · SHERLOCK 3CG TCS DISPLAY · Class 2
All models of Sherlock (9)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00801741124358), received between Mar 19, 2021 and Jul 28, 2022 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Application Program Freezes or Fails to Launch” (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.
Most reported problems
Device problems
- Application Program Freezes or Fails to Launch1
- Data Problem1
- Poor Quality Image1
- Unexpected Shutdown1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 28, 2022Data Problem; Data Problem
UNIT NOT TRACKING PICC PROPERLY, IT SHOWS PICC IS GOING TOWARDS NECK BUT THEY'RE GETTING A P-WAVE. THEY DO AN X-RAY CHECK TO VERIFY AND IT DOES SHOW THE PICC IS IN THE RIGHT LOCATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15122309 ↗MalfunctionAug 25, 2021Application Program Freezes or Fails to Launch; Application Program Freezes or Fails to Launch
SCREEN FREEZES AND REQUIRES A COMPLETE RE BOOT TO START.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12367469 ↗MalfunctionAug 18, 2021Poor Quality Image; Poor Quality Image
BACK BATTERY DOESN¿T STAY INTACT AND WHEN THEY TRY TO HOLD IT IN PLACE THEY GET LINES ACROSS THE SCREEN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12340388 ↗MalfunctionMar 19, 2021Unexpected Shutdown; Unexpected Shutdown
IT WAS REPORTED UNIT TURNING ITSELF OFF IN THE MIDDLE OF PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11532448 ↗
Other Catheter,intravascular,therapeutic,long-term greater than 30 days devices
- Groshong NXT ClearVue Catheter 7617405Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 deaths1,708 reports
- Groshong NXT ClearVue Catheter 7655405Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 deaths1,536 reports
- PowerPICC Catheter 3174118Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall402 reports
- L-Cath™ S/L PICC S/L 26GA (1.9F) x 30cmArgon Medical Devices, Inc. · Catheter,Intravascular,Therapeutic,Long-Term Greater Than 30 Days2 recalls245 reports
- PowerPICC SOLO2 Catheter 1194108DBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days2 recalls216 reports
- Broviac 0600520Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall265 reports
- Groshong® Catheter 7717405Bard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days279 reports
- PowerPICC® Catheters 1174108DBard Access Systems, Inc. · Catheter,intravascular,therapeutic,long-term greater than 30 days1 recall222 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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