Reported Sep 17, 2014 · Terminated

***Baxter***Buretrol Solution Set***105" (2.7 m)***150 mL Burette***Drip Chamber Filter Valve***3 Injection Sites Male…

Baxter Healthcare Corp.

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: Baxter Healthcare Corp · 1 Baxter Pkwy · Deerfield, IL · 60015-4625

Is this the product you have?

  • ***Baxter***Buretrol Solution Set***105" (2.7 m)***150 mL Burette***Drip Chamber Filter Valve***3 Injection Sites Male Luer Lock Adapter with***Retractable Collar***Fluid path is Sterile, Nonpyrogenic***Indications
  • for UseFor the administration of fluids from a container into the patient's vascular system through a vascular access device.***
Lot codes and dates
  • 2C7564- Buretrol Solution Set with 150mL INTERLINK Burette
  • lots
    • DR13E06019
    • DR13E07017
    • DR13E07025
    • DR13I14023
    • DR13I16010
    • DR13I16028
    • DR13I23016
    • DR13I23024
    • DR13J03033
    • DR13J04015
    • DR13J04023
    • DR13J08024
    • DR13J09014
    • DR13J09022
    • DR13J24021
    • DR13J24039
    • DR13K07024
    • DR13K08022
    • DR13K12024
    • DR13K13022
    • DR13K18021
    • DR13K19029
    • DR13K25026
    • DR13K26024
    • DR13L02023
    • DR13L03039
    • DR13L10018
    • DR13L11016
    • DR13L18011
    • DR13L18029
    • DR13L19035
    • DR14A09052
    • DR14A10035
    • DR14A23012
    • DR14A23020
    • DR14A29027
    • DR14A30017
    • DR14B06049
    • DR14B07013
    • DR14B07047
    • DR14B11023
    • DR14B13037
    • DR14B13045
    • DR14B14019
    • DR14B20016
    • DR14B20032
    • DR14B21014
    • DR14B26013
    • DR14B26039
    • DR14C05015
    • DR14C05031
Amount recalled
234196

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide

Why it was recalled

Baxter Healthcare Corporation is voluntarily issuing a recall for specific lots of Buretrol Solution set product codes due to complaints for separation between the burette chamber and the drip chamber. Affected product codes are: 2C7564, 2C8864 and 2H8864.

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.

Free recall alerts

Get alerted about new Baxter Healthcare Corp. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Mar 15, 2016 · Data as of Sep 19, 4:50 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.