PowerPICC Sherlock 3CGRecalls & reported problems across all models

We found 7 models of PowerPICC Sherlock 3CG by Bard Access Systems, Inc. in the FDA's device registry (GUDID). Together they are named in 6 adverse event reports in the FDA's MAUDE database, received between Apr 22, 2025 and May 11, 2026 — classified as 6 malfunctions.

The most frequently reported specific device problem is “Difficult or Delayed Separation” (3 reports).

2 FDA recall records name at least one of these models by its device identifier, 2 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

PowerPICC Sherlock 3CG recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. May 21, 2026Open, Classified

   Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.

   Z-2666-2026 · Root cause: Nonconforming Material/Component · Recall details · FDA record ↗

2. Mar 11, 2025Open, Classified

   Catheters indicated for short-or-long term access to the central venous system have tubing that exceeded melt flow index specification (higher), which could lead to increased material fatigue leaks, which could lead to infiltration, extravasation, discomfort, phlebitis, bleeding, air embolism, foreign body embolism, infection and interruption to therapy.

   Z-1507-2025 · Root cause: Process control · names 3 of these models · Recall details · FDA record ↗

Most reported PowerPICC Sherlock 3CG problems

PowerPICC Sherlock 3CG models

7 models, most reported first. Each model has its own page with its reports, recalls and device details.

• PowerPICC Sherlock 3CG CK000668B

  Catheter, intravascular, therapeutic, long-term greater than 30 days
  1 recall3 reports
• PowerPICC Sherlock 3CG CK000983

  Catheter, intravascular, therapeutic, long-term greater than 30 days
  1 recall0 reports
• PowerPICC Sherlock 3CG CK000746A

  Catheter, intravascular, therapeutic, long-term greater than 30 days
  1 recall0 reports
• PowerPICC Sherlock 3CG CK001067

  Catheter, intravascular, therapeutic, long-term greater than 30 days
  1 recall0 reports
• PowerPICC Sherlock 3CG CK000887A

  Catheter, intravascular, therapeutic, long-term greater than 30 days
  1 report
• PowerPICC Sherlock 3CG CK001062

  Catheter, intravascular, therapeutic, long-term greater than 30 days
  1 report
• PowerPICC Sherlock 3CG CK000631C

  Catheter, intravascular, therapeutic, long-term greater than 30 days
  1 report

Recent PowerPICC Sherlock 3CG adverse event reports

The 6 most recent reports across all models, in the reporter's own words as published by the FDA.

• MalfunctionMay 11, 2026Material Deformation

  IT WAS REPORTED BY THE CUSTOMER THAT DURING THE INITIAL ATTEMPT TO DILATE THE VEIN USING THE INTRODUCER, THE DILATOR FAILED TO FUNCTION AS EXPECTED. THE PATIENT DID NOT HAVE ANY ADVERSE EFFECTS AND DID NOT HAVE SKIN THAT WOULD LEAD ME TO THINK THE DILATOR WOULD FAIL. NO FURTHER INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25137723 ↗
• MalfunctionApr 23, 2026Difficult or Delayed Separation

  IT WAS REPORTED THE SHEATH THAT BREAK AWAY DID NOT BREAK APART PROPERLY. NO FURTHER INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24966339 ↗
• MalfunctionApr 23, 2026Difficult or Delayed Separation

  IT WAS REPORTED THE SHEATH THAT BREAK AWAY DID NOT BREAK APART PROPERLY. NO FURTHER INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24966309 ↗
• MalfunctionFeb 6, 2026Fluid/Blood Leak

  IT WAS REPORTED BY CUSTOMER THAT THE CATHETER THAT WAS IMPLANTED IN (B)(6). RECENTLY, THE PATIENT NOTICED A PROBLEM, AND UPON EXAMINATION, THE DOCTOR DISCOVERED A LEAK IN THE PICC LINE. THE PICC WAS SUBSEQUENTLY REPLACED. NO FURTHER DETAILS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24276980 ↗
• MalfunctionFeb 3, 2026Difficult or Delayed Separation

  IT WAS REPORTED ONE OF OUR PICC RNS ATTEMPTED TO PLACE A PICC LINE ON (B)(6) 2026. THEY ADVISED THAT THE SHEATH WAS NOT SCORED AND COULD NOT BE BROKEN, THUS MALFUNCTIONING LEADING TO A SECOND PROCEDURE FOR AN ALREADY ANXIOUS PATIENT. NO OTHER INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24251881 ↗
• MalfunctionApr 22, 2025Tear, Rip or Hole in Device Packaging; Tear, Rip or Hole in Device Packaging

  IT WAS REPORTED BY CUSTOMER THAT INSIDE OF KIT SMELLS MOLDY- HORRIBLE SMELL COMING FROM INSIDE KIT. NO OTHER INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21882912 ↗

Other Bard Access Systems, Inc. products

• Port Access Needle122 models · 3,744 reports · 3 recalls
• Groshong NXT ClearVue Catheter8 models · 3,266 reports
• PowerPort ClearVUE27 models · 1,993 reports · 15 recalls
• Site~Rite 8 Ultrasound System11 models · 1,965 reports
• PowerPort M.R.I., ChronoFlex22 models · 1,642 reports · 1 recall
• PowerPICC Provena116 models · 1,337 reports · 2 recalls
• PowerPort M.R.I., Groshong10 models · 1,285 reports
• Navarre15 models · 1,228 reports