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D-1550-2014 Class I Terminated

Recalled by Baxter Healthcare Corp. — Deerfield, IL

FDA drug recall D-1550-2014 was initiated by Baxter Healthcare Corp. on May 12, 2014 and is designated Class I. Reason for recall: Presence of Particulate Matter; blue polyisoprene shavings found inside the bag port tubes The recall status is terminated (terminated Jun 29, 2015). Affected quantity: 4,200 containers.

Recall Details

Product Type: Drugs
Report Date: Aug 27, 2014
Initiation Date: May 12, 2014
Termination Date: Jun 29, 2015
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 4,200 containers

Product Description

0.9 % Sodium Chloride Injection, USP, 1000 mL in VIAFLEX Plastic Container, Baxter Healthcare Corporation, Deerfield, IL 60015

Reason for Recall

Presence of Particulate Matter; blue polyisoprene shavings found inside the bag port tubes

Distribution Pattern

Nationwide

Code Information

Lot C931923, exp 8/31/2015

Source

Dataset: openFDA drug recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for D-1550-2014
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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