Reported Jul 7, 2021 · Terminated
5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with 70 cm Guidewire Unit Label: PowerPICC REF CK000340B BARD…
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?
- 5 Fr IR PowerPICC Convenience Kit Catheter Dual
- Lumen with 70 cm Guidewire Unit LabelPowerPICC REF CK000340B BARD MYPICC KIT 5F French Size Dual-Lumen 70cm Guidewire
- Lot codes and dates
- Catalog (REF) NumberCK000340B
- UDI Code(01)00801741126697
- Lot Number20BBK658
- Amount recalled
- 30 kits
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
- RI
Why it was recalled
Catheter convenience kits contain the incorrect guidewire. Kits were labeled with 70cm guidewires, but contained a 50cm guidewire.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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