Reported Jun 22, 2016 · Terminated

Vaxcel PICC with PASV IR-145 Kit under the following labels

Navilyst Medical, Inc., an AngioDyamics Company

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: Navilyst Medical, Inc., an AngioDyamics Company · 10 Glens Falls Tech Park · Glens Falls, NY · 12801-3864

Is this the product you have?

Vaxcel PICC with PASV IR-145 Kit under the following labels

3 of 3 products

Products covered by this recall
#Product as published
14F, UPN M001454580, Rx ONLY
25F, UPN M001454630, Rx ONLY &
36F, UPN M001454780, Rx ONLY The Vaxcel PICC with PASV is indicated for use in establishing peripheral access to the central venous system for administration of fluids including, but not limited to, hydration agents, antibiotics, chemotherapy, analgesics, nutritional therapy, and blood products. It is also indicated for blood specimen withdrawal. This product is intended for central venous access in adults, children and infants who require intravenous (IV) therapy.
Lot codes and dates

3 of 3 products

Products covered by this recall
#Product as published
14748893, 4766101, 4773293 & 4814220 with Use By Range 2016-05-31 to 2016-10-31. Batch/Lots
24752348, 4784466, 4735032, 4738833, 4765395 & 4814222 with Use By Range 2016-05-31 to 2016-07-31. Batch/Lots
34752881, 4765393 & 4942171 with Use By Range 2016-05-31 to 2017-09-30.
Amount recalled
2,260 units

This recall covers 23 products

The agency filed one notice per product. You are reading one of them; the other 22 are below.

10 more are in the archive.

Where it was sold

Why it was recalled

PICC catheters that contain valve(s) manufactured prior to July 15, 2014 lack a manufacturing specification change that reduces the incidence of hemolysis during blood sampling through the PICC catheter.

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 (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jun 11, 2018 · Data as of Sep 19, 5:59 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.