Sherlock 9770353Recalls & reported problems
Bard Access Systems, Inc. · Sherlock 3CG+ Small Sensor · Class 2
All models of Sherlock (9)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00801741163098), received between Jan 19, 2023 and Sep 12, 2024 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Data Problem” (3 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Data Problem3
- Break2
- No Apparent Adverse Event2
- Defective Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 12, 2024No Apparent Adverse Event; Data Problem; No Apparent Adverse Event; Data Problem
IT WAS REPORTED, SENSOR IS GIVING INACCURATE, ERRATIC READINGS. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20201877 ↗MalfunctionJul 3, 2024Data Problem; Data Problem
IT WAS REPORTED BY CUSTOMER THAT PREVIOUSLY PLACED PICCS USING SMALL SHERLOCK SENSOR WERE CONFIRMED WITH MAX P WAVE, BUT X-RAYS SHOWED TOO DEEP/SHORT. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19666769 ↗MalfunctionOct 26, 2023No Apparent Adverse Event; Data Problem; No Apparent Adverse Event; Data Problem
IT WAS REPORTED READINGS ARE INTERMITTENTLY SHOWING THE WRONG LOCATION ON THE PATIENT. "NOT GETTING AN INTRAVASCULAR WAVEFORM ONCE THE PICC IS CONNECTED TO THE SENSOR."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18011504 ↗MalfunctionApr 3, 2023Break; Defective Component; Break; Defective Component
IT WAS REPORTED THE CORD IS PULLING AWAY AT THE STRAIN RELIEF, EXPOSING WIRING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16665939 ↗MalfunctionJan 19, 2023Break; Break
IT WAS REPORTED THE STRAIN RELIEF WIRES ARE EXPOSED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16211304 ↗
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- 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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