FDAFDA · Food and drugs·Recall number D-1162-2014
5% Dextrose Injection, USP, 100 mL Single dose VIAFLEX plastic containers, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015 USA, Product code 2B0089, NDC 0338-0017-38.
Published March 26, 2014 · Recall initiated: November 21, 2013
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of Paticulate Matter; Baxter is issuing a voluntary recall for these IV solutions due to particulate matter found in the solution identified as polyester and cotton fibers, adhesive-like mixture, polyacetal particles, thermally degraded PVC, black polypropylene and human hair embedded in the plastic bag
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- DEXTROSE
- Manufacturer
- Baxter Healthcare Corp.
- Distributor
- Nationwide, Puerto Rico, Singapore, Saudi Arabia and United Arab Emirates.
- Lot
- Lot #: P285288, Exp 11/13
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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