Reported Oct 3, 2012 · Terminated

5% Dextrose Injection USP, packaged in a) 250 mL AVIVA Container, product code 6E0062, NDC 0338-6346-02; b) 500 mL…

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. · Route 120 And Wilson Rd · Round Lake, IL · 60073-9799

Is this the product you have?

3 of 3 products

Products covered by this recall
Model / numberProduct as published
6E00625% Dextrose Injection USP, packaged in a) 250 mL AVIVA Container, , NDC 0338-6346-02
6E0063500 mL AVIVA Container, , NDC 0338-6346-03
Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA
Lot codes and dates

27 of 27 products

Products covered by this recall
#Product as published
1C841114, C841254, Exp 09/12
2C842229, C842898, C843037, C843326, C844209, Exp 10/12
3C844456, C844928, C846089, C846246, C847178, Exp 11/12
4C848044, C848804, C849869, C849810, C850313, Exp 12/12
5C852574, C852673, C853168, C853275, C853473, Exp 01/13
6C854331, C855098, C855551, Exp 02/13
7C856690, C856815, C857813, Exp 03/13
8C858829, C858951, C859884, C860049, C860304, C860304A, C860452, C861138, Exp 04/13
9C861252, C861971, C862748, C862854, Exp 05/13
10C865576, C865683, C866079, Exp 06/13
11C866947, C867283, C867424, C867960, C868455, Exp 07/13
12C818039, Exp 09/12
13C821793, Exp 10/12
14C824276, C825679, Exp 11/12
15C828350, Exp 12/12
16C830323, C832105, Exp 01/13
17C834986, C836114, Exp 03/13
18C840736, Exp 04/13
19C843433, Exp 05/13
20C844829, C845784, Exp 06/13
Amount recalled
753,941 containers

This recall covers 5 products

The agency filed one notice per product. You are reading one of them; the other 4 are below.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

Chemical Contamination: The IV solutions were packaged in AVIVA containers which may contain trace levels of cumene hydroperoxide (CHP).

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

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Where this came from

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

Read the FDA (openFDA drug enforcement) notice

Notice updated May 4, 2015 · Data as of Sep 19, 7:14 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.