D-1335-2015 Class I Terminated
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