Sodium Chloride Injection (Baxter) – Chemical Contamination (2012)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
0.9% Sodium Chloride Injection USP, packaged in a) 250 mL AVIVA Container, product code 6E1322, NDC 0338-6304-02; b) 500 mL AVIVA Container, product code 6E1323, NDC 0338-6304-03; Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA
Brand
Baxter Healthcare Corp.
Lot Codes / Batch Numbers
Lot #: a) C840892, C841007, C841403, Exp 09/12, C842377, C842757, C843748, C843946, Exp 10/12, C844332, C845065, C845198, C845347, C846873, C847301, C847608, Exp 11/12, C848481, C848937, C849554, C850180, Exp 12/12, C850966, C851097, C851212, C852459, C853044, C853614, Exp 01/13, C853747, C854455, C854711, C854836, C854943, C856013, C856138, Exp 02/13, C856948, C858027, Exp 03/13, C858712, C859066, C859199, C859389, C860569, C861021, Exp 04/13, C861856, C862953, C863076, C863183, Exp 05/13, C865188, C865824, C866178, C866178A, Exp 06/13, C867168, C868117, C868570, C868703, Exp 07/13, b) C818187, C819367, Exp 09/12, C821686, Exp 10/12, C823377, Exp 11/12, C826255, C828111, C828228, Exp 12/12, C830455, C830604, Exp 01/13, C832964, C833152, Exp 02/13, C839134, C840587, Exp 04/13, C842740, C843649, Exp 05/13, C844647, C845941, C847038, Exp 06/13, C848184, C849117, C850545, Exp 07/13, C850842, C851568, C852806, Exp 08/13, C853853, C854216, C854216A, C855213, Exp 09/13, C856567, C858142, C858258, Exp 10/13, C858613, C859777, C859777A, C860916, Exp 11/13, C861617, C861724, Exp 12/13, C865311, C866285, Exp 01/14, C866632, C866830, Exp 02/14
Products Sold
Lot #: a) C840892, C841007, C841403, Exp 09/12; C842377, C842757, C843748, C843946, Exp 10/12; C844332, C845065, C845198, C845347, C846873, C847301, C847608, Exp 11/12; C848481, C848937, C849554, C850180, Exp 12/12; C850966, C851097, C851212, C852459, C853044, C853614, Exp 01/13; C853747, C854455, C854711, C854836, C854943, C856013, C856138, Exp 02/13; C856948, C858027, Exp 03/13; C858712, C859066, C859199, C859389, C860569, C861021, Exp 04/13; C861856, C862953, C863076, C863183, Exp 05/13; C865188, C865824, C866178, C866178A, Exp 06/13; C867168, C868117, C868570, C868703, Exp 07/13; b) C818187, C819367, Exp 09/12; C821686, Exp 10/12; C823377, Exp 11/12; C826255, C828111, C828228, Exp 12/12; C830455, C830604, Exp 01/13; C832964, C833152, Exp 02/13; C839134, C840587, Exp 04/13; C842740, C843649, Exp 05/13; C844647, C845941, C847038, Exp 06/13; C848184, C849117, C850545, Exp 07/13; C850842, C851568, C852806, Exp 08/13; C853853, C854216, C854216A, C855213, Exp 09/13; C856567, C858142, C858258, Exp 10/13; C858613, C859777, C859777A, C860916, Exp 11/13; C861617, C861724, Exp 12/13; C865311, C866285, Exp 01/14; C866632, C866830, Exp 02/14
Baxter Healthcare Corp. is recalling 0.9% Sodium Chloride Injection USP, packaged in a) 250 mL AVIVA Container, product code 6E1322, NDC due to Chemical Contamination: The IV solutions were packaged in AVIVA containers which may contain trace levels of cumene hydroperoxide (CHP).. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA drug enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Chemical Contamination: The IV solutions were packaged in AVIVA containers which may contain trace levels of cumene hydroperoxide (CHP).
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm, their healthcare provider, or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 7, 2026