Reported Oct 3, 2012 · Terminated

0.9% Sodium Chloride Injection USP, packaged in a) 250 mL AVIVA Container, product code 6E1322, NDC 0338-6304-02; b)…

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
6E13229% Sodium Chloride Injection USP, packaged in a) 250 mL AVIVA Container, , NDC 0338-6304-02
6E1323500 mL AVIVA Container, , NDC 0338-6304-03
Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA
Lot codes and dates

28 of 28 products

Products covered by this recall
#Product as published
1C840892, C841007, C841403, Exp 09/12
2C842377, C842757, C843748, C843946, Exp 10/12
3C844332, C845065, C845198, C845347, C846873, C847301, C847608, Exp 11/12
4C848481, C848937, C849554, C850180, Exp 12/12
5C850966, C851097, C851212, C852459, C853044, C853614, Exp 01/13
6C853747, C854455, C854711, C854836, C854943, C856013, C856138, Exp 02/13
7C856948, C858027, Exp 03/13
8C858712, C859066, C859199, C859389, C860569, C861021, Exp 04/13
9C861856, C862953, C863076, C863183, Exp 05/13
10C865188, C865824, C866178, C866178A, Exp 06/13
11C867168, C868117, C868570, C868703, Exp 07/13
12C818187, C819367, Exp 09/12
13C821686, Exp 10/12
14C823377, Exp 11/12
15C826255, C828111, C828228, Exp 12/12
16C830455, C830604, Exp 01/13
17C832964, C833152, Exp 02/13
18C839134, C840587, Exp 04/13
19C842740, C843649, Exp 05/13
20C844647, C845941, C847038, Exp 06/13
Amount recalled
897,496 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, 5:46 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.