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PowerPICC Provena S1173108D1Recalls & reported problems

Bard Access Systems, Inc. · Catheter Placement Kit · Class 2 · Implant

All models of PowerPICC Provena (116)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741154720), received between Apr 22, 2022 and Apr 22, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (1 report).

1 FDA recall record name this device's 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, 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 18, 2026.

Recalls naming this device

  1. May 21, 2026Class IIOpen, 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 · Recall details · FDA record ↗

Most reported problems

Device problems

  • Device Dislodged or Dislocated1

Patient problems

  • 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.

  • MalfunctionApr 22, 2022Device Dislodged or Dislocated; Device Dislodged or Dislocated

    IT WAS REPORTED VIA MS&S "NURSE CALLING ON BEHALF OF A PATIENT WHO SHE BELIEVES HAS AN OCCLUDED 3F POWERPICC PROVENA (REF (B)(4), LOT# REFR0253). THE PATIENT'S PICC WAS IMPLANTED ON (B)(6) 2022. ALSO, SHE BELIEVES THE CATHETER TIP IS NOT IN THE RIGHT LOCATION. THE DOCUMENTATION STATED ON 1-3CM IS OUT OF THE ARM BUT IT LOOKS LIKE A FOOT OF THE CATHETER IS OUT OF THE ARM. SHE TRIED TO ASPIRATE FOR BLOOD WITHOUT SUCCESS. THE PATIENT WAS TOLD TO CALL MI NUMBER IF THERE WAS ANY PROBLEMS WITH THE PICC LINE" MS&S RESPONSE: INFORMED FOR CATHETER OCCLUSION WE TYPICALLY RECOMMEND CONTACTING THE PHYSICIAN TO SEE IS TPA CAN BE ORDERED FOR POSSIBLE FIBRIN BUILDUP. RECOMMENDED CONTACTING THE DOCTOR SO THE CATHETER CAN BE ASSESSED IF THE PICC CATHETER IS MALPOSITION

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14190074 ↗

Other Catheter, intravascular, therapeutic, long-term greater than 30 days devices

All Catheter, intravascular, therapeutic, long-term greater than 30 days devices →

Sources and updates

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