D-1335-2015 Class I Terminated

Recalled by Baxter Healthcare Corp. — Deerfield, IL

FDA drug recall D-1335-2015 was initiated by Baxter Healthcare Corp. on Jul 17, 2015 and is designated Class I. Reason for recall: Presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled. The recall status is terminated (terminated Dec 1, 2016). Affected quantity: 133,600 bags.

Recall Details

Product Type
Drugs
Report Date
Aug 26, 2015
Initiation Date
Jul 17, 2015
Termination Date
Dec 1, 2016
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
133,600 bags

Product Description

0.9% Sodium Chloride Injection USP MINI-BAG Plus Container, 100 mL VIAFLEX Single Dose Container bags, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Product Code 2B0043, NDC 0338-0553-18.

Reason for Recall

Presence of Particulate Matter: Customer complaint for an insect found free floating inside a single bag for each lot recalled.

Distribution Pattern

Nationwide

Code Information

Lot#: P327635, Exp 12/15

Source

Dataset
openFDA drug recall enforcement reports
FDA record
This recall in openFDA (JSON)
Enforcement Report
Search FDA's Enforcement Report for D-1335-2015
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.