PowerPICC Provena Sherlock 3CGRecalls & reported problems across all models

We found 3 models of PowerPICC Provena Sherlock 3CG by Bard Access Systems, Inc. in the FDA's device registry (GUDID). Together they are named in 1 adverse event report in the FDA's MAUDE database, received between Jun 16, 2026 and Jun 16, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Contamination /Decontamination Problem” (1 report).

1 FDA recall record name at least one of these models by its device identifier, 1 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 Provena 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-2664-2026 · Root cause: Nonconforming Material/Component · names 2 of these models · Recall details · FDA record ↗

Most reported PowerPICC Provena Sherlock 3CG problems

PowerPICC Provena Sherlock 3CG models

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

• PowerPICC Provena Sherlock 3CG CK001066

  Catheter, intravascular, therapeutic, long-term greater than 30 days
  1 recall0 reports
• PowerPICC Provena Sherlock 3CG CK001068

  Catheter, intravascular, therapeutic, long-term greater than 30 days
  1 recall0 reports
• PowerPICC Provena Sherlock 3CG CK000669B

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

Recent PowerPICC Provena Sherlock 3CG adverse event reports

The 1 most recent reports across all models, in the reporter's own words as published by the FDA.

• MalfunctionJun 16, 2026Contamination /Decontamination Problem

  IT WAS REPORTED THERE IS HAIR IN THE KIT. NO FURTHER INFORMATION WAS PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25521556 ↗

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