Reported Jul 8, 2026 · Ongoing · Updated Sep 16, 2026

CK000525B PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236129 CK000883 PowerPICC Provena…

Bard Access Systems, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Bard Access Systems, Inc. · 605 N 5600 W · Salt Lake City, UT · 84116-3738

Is this the product you have?

  • CK000525B PowerPICC Provena SOLO
  • Catheter 4 Fr Dual-Lumen UDI-DI Code00801741236129 CK000883 PowerPICC Provena
  • Catheter 4 Fr Dual-Lumen UDI-DI Code00801741188800 CK000884A PowerPICC Provena SOLO
  • Catheter 4 Fr Dual-Lumen UDI-DI Code00801741219177 CK001000 PowerPICC Provena SOLO
  • Catheter 4 Fr Dual-Lumen UDI-DI Code00801741223020 CK001066 PowerPICC Provena
  • Catheter 4 Fr Dual-Lumen UDI-DI Code00801741228544 CK001068 PowerPICC Provena
  • Catheter 4 Fr Dual-Lumen UDI-DI Code00801741228728 S1173108D PowerPICC Provena
  • Catheter 3 Fr Single-Lumen UDI-DI Code00801741130342 S1173108D1 PowerPICC Provena
  • Catheter 3 Fr Single-Lumen UDI-DI Code00801741154720 S1173108D4 PowerPICC Provena
  • Catheter 3 Fr Single-Lumen UDI-DI Code00801741155031 S1173108D5 PowerPICC Provena
  • Catheter 3 Fr Single-Lumen UDI-DI Code00801741155130 S1173108D6 PowerPICC Provena
  • Catheter 3 Fr Single-Lumen UDI-DI Code00801741232190 S1193108D3 PowerPICC Provena SOLO
  • Catheter 3 Fr Single-Lumen UDI-DI Code00801741154980 S1193108D4 PowerPICC Provena SOLO
  • Catheter 3 Fr Single-Lumen UDI-DI Code00801741155086 S1193108D5 PowerPICC Provena SOLO
  • Catheter 3 Fr Single-Lumen UDI-DI Code00801741155185 S1193108PD PowerPICC Provena SOLO
  • Catheter 3 Fr Single-Lumen UDI-DI Code00801741134135 S1274108D PowerPICC Provena
  • Catheter 4 Fr Dual-Lumen UDI-DI Code00801741130366 S1274108D4 PowerPICC Provena
  • Catheter 4 Fr Dual-Lumen UDI-DI Code00801741155055 S1274108D5 PowerPICC Provena
  • Catheter 4 Fr Dual-Lumen UDI-DI Code00801741155154 S1294108D PowerPICC Provena SOLO
  • Catheter 4 Fr Dual-Lumen UDI-DI Code00801741130373 S1294108D2 PowerPICC Provena
  • Catheter 4 Fr Dual-Lumen UDI-DI Code00801741154898 S1294108D4 PowerPICC Provena SOLO
  • Catheter 4 Fr Dual-Lumen UDI-DI Code00801741155109 S1294108D5 PowerPICC Provena SOLO
  • Catheter 4 Fr Dual-Lumen UDI-DI Code00801741155208 S3173108 PowerPICC Provena
  • Catheter 3 Fr Single-Lumen UDI-DI Code00801741130144 S3274108D PowerPICC Provena
  • Catheter 4 Fr Dual-Lumen UDI-DI Code00801741130403 S9274108D PowerPICC Provena
  • Catheter 4 Fr Dual-Lumen UDI-DI Code00801741130441 The PowerPICC Provena Catheters and PowerPICC Provena Catheter with SOLO Valve Technology are indicated for short and long term peripheral access to central venous system for intravenous therapy, blood sampling, power injection of contrast media, and allow for central venous pressure monitoring. For central venous pressure monitoring, it is recommended that a catheter lumen of 20 guage or larger be used
Lot codes and dates

25 of 25 products

Products covered by this recall
#BarcodesProduct as published
100801741188800Lot Numbers: REKW2510 REKX3786 CK000883 PowerPICC Provena Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741188800
200801741219177Lot Number: REKX3767 CK000884A PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741219177
300801741223020Lot Number: REKX0133 CK001000 PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741223020
400801741228544Lot Number: REKY1171 CK001066 PowerPICC Provena Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741228544
500801741228728Lot Number: REKX0087 CK001068 PowerPICC Provena Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741228728
600801741130342Lot Number: REKW1569 S1173108D PowerPICC Provena Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741130342
700801741154720Lot Number: REKX3449 S1173108D1 PowerPICC Provena Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741154720
800801741155031Lot Number: REKU2923 S1173108D4 PowerPICC Provena Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741155031
900801741155130Lot Numbers: REKV3208 REKW2482 S1173108D5 PowerPICC Provena Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741155130
1000801741232190Lot Number: REKX0070 S1173108D6 PowerPICC Provena Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741232190
1100801741154980Lot Number: REKY0141 S1193108D3 PowerPICC Provena SOLO Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741154980
1200801741155086Lot Number: REKV3188 S1193108D4 PowerPICC Provena SOLO Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741155086
1300801741155185Lot Numbers: REKV3240 REKW0961 S1193108D5 PowerPICC Provena SOLO Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741155185
1400801741134135Lot Number: REKW1468 S1193108PD PowerPICC Provena SOLO Catheter 3 Fr Single-Lumen UDI-DI Code: 00801741134135
1500801741130366Lot Numbers: REKV3256 REKY1690 S1274108D PowerPICC Provena Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741130366
1600801741155055Lot Number: REKW1461 S1274108D4 PowerPICC Provena Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741155055
1700801741155154Lot Number: REKW2520 S1274108D5 PowerPICC Provena Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741155154
1800801741130373Lot Number: REKW1458 S1294108D PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741130373
1900801741154898Lot Number: REKV2247 S1294108D2 PowerPICC Provena Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741154898
2000801741155109Lot Numbers: REKW0952 REKX2229 S1294108D4 PowerPICC Provena SOLO Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741155109
Amount recalled
29,490

This recall covers 14 products

The agency filed one notice per product. You are reading one of them; the other 13 are below.

1 more are in the archive.

Where it was sold

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (Enforcement Report)

Read the FDA (weekly enforcement report) notice

Data as of Sep 19, 5:01 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.