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D-1159-2014 Class I Terminated

Recalled by Baxter Healthcare Corp. — Deerfield, IL

FDA drug recall D-1159-2014 was initiated by Baxter Healthcare Corp. on Nov 18, 2013 and is designated Class I. Reason for recall: Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose. The recall status is terminated (terminated Sep 20, 2016). Affected quantity: 7,068 bags.

Recall Details

Product Type: Drugs
Report Date: Mar 26, 2014
Initiation Date: Nov 18, 2013
Termination Date: Sep 20, 2016
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 7,068 bags

Product Description

Clinimix E 4.25/10 sulfite-free (4.25% Amino Acid with Electrolytes in 10% Dextrose with Calcium) Injection, 2000 mL CLARITY Dual Chamber Container bag, Rx only. Dist: Baxter Healthcare Corporation, One Baxter Parkway, Deerfield, IL 60015. NDC 0338-1115-04.

Reason for Recall

Presence of Particulate Matter: Particulate matter includes wood, sodium citrate and dextrose.

Distribution Pattern

US Nationwide

Code Information

Lot#: P275883, Exp 10/2013

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-1159-2014
openFDA file date: Oct 27, 2026
Loaded by RegDataLab: Oct 29, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.

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